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Baptist Hospital of Miami is seeking Neuro anesthesia-trained anesthesiologists to join our distinguished team, situated in the sunny and vibrant Miami!! The successful candidate will be experienced in neurosurgical and neuro interventional radiology procedures and will have strong general anesthesiologist skills. Baptist Health Neuroscience Center provides the most advanced techniques to treat the brain, spine and nervous system. Our neuro anesthesiologists work closely with neuro medicine and neurosurgical surgical specialists in a collegial environment that fosters collaboration. Baptist Hospital is a growing and established group, one of Miami's finest! Practice Highlights: * Care Team Model of 37 Anesthesiologists and 44 Allied Health, both CRNAs and CAAs. * Broad case mix including, but not limited to, Neuro, Vascular, General, OB/Gen, Ortho, IR, GI, Cardiac, Interventional Cardiac, Interventional Neuroradiology and Pedi. * Annual case volume of 40K * High Acuity, active OB and Cases from Cancer center, advanced Endo * 5.-Teams cover main hospital, 24 OR's, 16 Interventional suites, 4 Endoscopy suites, 2 C/S rooms, Plus 10 ASC rooms. * Call shared equitably amongst team and can be taken from home. * Competitive salary, Start date bonus and Relocation. * Benefits eligible day one of employment- No waiting period! * Company pays 100% of professional liability insurance with tail coverage. For more information about this opportunity, please contact Maryann Holthus, Clinical Recruiter at 734-259-9375 or Envision Physician Services is a dynamic physician- and clinician-led medical group that has been offering exceptional career opportunities for more than 60 years. With our national network of clinicians who are committed to delivering high-quality care, Envision Physician Services is nationally recognized for delivering clinical excellence supported by innovation, integration and exceptional leadership. Candidates considering becoming a teammate at Envision Physician Services will find full-time, part-time and independent contractor opportunities available in a variety of community types, from rural and underserved communities to major metropolitan areas; practice settings, from small hospitals to academic health systems; and job levels, from entry level to senior management. Envision teammates also benefit from the following resources: \t • Strong leadership at local, regional and national levels\t, • Exceptional quality of practice backed by comprehensive support services\t, • Optimal care teams with flexible and equitable scheduling options\t, • A-rated professional liability insurance\t, • Extensive variety of practice settings coast-to-coast\t, • Competitive compensation, including several benefit options\t, • Opportunities for professional development, mentoring and career advancement\t, • Clinician mental health and well-being support\t, • Comprehensive education and training on leadership, management and clinical best practices, including a wide variety of CME programs\t, • Clinical and scientific research opportunities *Benefits vary by division, clinical specialty and employment status.

Sylvester Comprehensive Cancer Center, part of the University of Miami Health System and the University of Miami Miller School of Medicine is initiating a search for a Staff Medical Oncologist. Core Job Functions: Develops and carries out a comprehensive medical treatment plan addressing biological, psychological, and sociocultural domains. Performs physical assessment of patients in a logical and respectful manner. Prescribes medical treatment and clinical drugs to patients. Gathers essential and accurate information through the review of pertinent records and interviews with the patient, family members, caregivers, and other health professionals. Reports to the responsible physician and complies with policy co-sig. Reports hazardous or unsafe conditions, equipment malfunction, and supply instrumentation inadequacies to appropriate personnel. Reports all Quality Assurance (QA) incidences, including mediation errors, to responsible physician using department guidelines. Assumes responsibility for increasing knowledge and expertise by attending continuing educational offerings. Makes informed decisions about interventions based on patient information and preference, up-to-date scientific evidence in the field, and clinical judgment. Maintains confidentiality of all patient information according to federal and state guidelines and regulations. Adheres to University and unit-level policies and procedures and safeguards University assets. Department Specific Functions: Incumbent will also serve as an instructor and as an attending physician in the Division of Medical Oncology, with focus on the care and treatment of patients with General Med Onc cancers. This will include outpatient care supervised by senior faculty with expertise in treatment and management of these cancers, as well as on-call coverage and weekend/rotations. Incumbent will have a focus in the treatment of malignant cancers, to include research protocols, leading to peer-reviewed publications and funded clinical trials. Incumbent will be responsible for the development of novel clinical and translational protocols for treatment of patients with malignancies. Core Qualifications: MD/DO required Board certification and/or eligibility in Hematology and/or Oncology required. Certification in relevant specialty or field required

General Anesthesiologist opportunity at a Level I Trauma Center in Miami, FL with EXCELLENT COMPENSATION & PTO, $75K Start Date Bonus! Envision Physician Services is seeking a BC/BE, General Anesthesiologist to join the growing practice at HCA Florida Kendall Regional Hospital located in Miami, Florida. This opportunity is best suited for an individual that is comfortable handling complex adult cases including trauma and is also interested in providing cardiac services. Practice Highlights: * Level I Trauma Center * GME Anesthesia residency accredited program * Care Team model: 22 Physicians and 27 CRNA's * Approximately 16,000 annual cases. * 14 state-of-the-art OR's * Mix of cases including General, OB, Ortho, vascular, ENT, Trauma, GI/Cardiovascular Lab, and Peds. * 80% adult trauma and 20% pediatrics * 1:3 or 1:4 supervision * Call requirements: Once a week in-house (3p-7a) * PTO to include 8 & 9 weeks * Medical, dental, vision, short-term/long-term disability, 401(k) contribution, health savings + more! * Malpractice provided For more information please contact Clinical Recruiter, Maryann Holthus at: 734 259 9375 or Envision Physician Services is a dynamic physician- and clinician-led medical group that has been offering exceptional career opportunities for more than 60 years. With our national network of clinicians who are committed to delivering high-quality care, Envision Physician Services is nationally recognized for delivering clinical excellence supported by innovation, integration and exceptional leadership. Candidates considering becoming a teammate at Envision Physician Services will find full-time, part-time and independent contractor opportunities available in a variety of community types, from rural and underserved communities to major metropolitan areas; practice settings, from small hospitals to academic health systems; and job levels, from entry level to senior management. Envision teammates also benefit from the following resources: \t • Strong leadership at local, regional and national levels\t, • Exceptional quality of practice backed by comprehensive support services\t, • Optimal care teams with flexible and equitable scheduling options\t, • A-rated professional liability insurance\t, • Extensive variety of practice settings coast-to-coast\t, • Competitive compensation, including several benefit options\t, • Opportunities for professional development, mentoring and career advancement\t, • Clinician mental health and well-being support\t, • Comprehensive education and training on leadership, management and clinical best practices, including a wide variety of CME programs\t, • Clinical and scientific research opportunities *Benefits vary by division, clinical specialty and employment status.

Envision is seeking an accomplished Emergency Department Medical Director to join this high profile and flagship hospital situated in sunny and vibrant Miami! This is one of the few positions in Emergency Medicine that combines the complexities of a large sophisticated medical center with the reward of working in a state-of-the-art Hospital/Emergency Department coupled with the extensive resources and support programs made available by Envision. Qualified Candidates: * Must be Board Certified in Emergency Medicine & clinically active in Emergency Medicine * Have previous leadership / administrative experience * Proven track record of implementing metrics/goals * Have strong administrative and team building skills * Excellent interpersonal and communication skills Position Profile: * Annual ED Volume: 90,000 * 80-bed ED, plus 14-bed Fast Track * Adult-only ED; pediatrics separate * 2 Assistant Medical Directors * Level II Critical Care Facility * Cerner EMR * Admission Rate: 38% * Excellent coverage with 9- and 10-hour shifts * Advanced Practice Provider and Scribe coverage * All subspecialties available * Long-term, stable contract * Professional and collegial work environment Envision Physician Services is a dynamic physician- and clinician-led medical group that has been offering exceptional career opportunities for more than 60 years. With our national network of clinicians who are committed to delivering high-quality care, Envision Physician Services is nationally recognized for delivering clinical excellence supported by innovation, integration and exceptional leadership. Candidates considering becoming a teammate at Envision Physician Services will find full-time, part-time and independent contractor opportunities available in a variety of community types, from rural and underserved communities to major metropolitan areas; practice settings, from small hospitals to academic health systems; and job levels, from entry level to senior management. Envision teammates also benefit from the following resources: \t • Strong leadership at local, regional and national levels\t, • Exceptional quality of practice backed by comprehensive support services\t, • Optimal care teams with flexible and equitable scheduling options\t, • A-rated professional liability insurance\t, • Extensive variety of practice settings coast-to-coast\t, • Competitive compensation, including several benefit options\t, • Opportunities for professional development, mentoring and career advancement\t, • Clinician mental health and well-being support\t, • Comprehensive education and training on leadership, management and clinical best practices, including a wide variety of CME programs\t, • Clinical and scientific research opportunities *Benefits vary by division, clinical specialty and employment status.

Envision Physician Services is seeking a full-time BC/BE Anesthesiologist with Cardiac experience to join our dynamic, well established team of 17 physicians and 24 APPs at HCA Florida Mercy Hospital in Miami, FL! Cardiac fellowship is not required!! Be in the heart of Miami and enjoy all that it has to offer, while being fully supported by your Envision Colleagues who staff the emergency department and provide hospitalist services. This opportunity includes Start Date Bonus and Relocation Stipend Practice Profile: * Physician-led on the local, regional, and national level * Smaller, collegial teams with day-to-day operational control fully supported by the tools and resources from a leading national medical group * Anesthesia team comprised of 17 Physicians and 24 APP's * Annual case volume of 12,000 with 120-200 cardiac cases annually * ANES case mix includes General, Ortho, Plastics, ENT, Urology, Vascular, Neuro and GYN * Case Mix- 33% Cardiac / 67% General ANES * Cardiac cases consist of CABG, Valve Replacement, Aortic surgery, TEVAR, TAVR, Mitra Clip, EP requiring TEE: Watchman, ECHO * Physicians perform 100% of their own open hearts and have an APP for structural hearts * TEE certified preferred, but not required. * Cardiac Fellowship is not required * Cardiac call only (can volunteer to take general): one week per month cardiac call back is rare! * Highly competitive compensation package * Start Date Bonus-$100K * Relocation Stipend * CME allowance * Malpractice and tail coverage provided * Full health benefits on day one * 401k contribution For more information about this opportunity, please contact Maryann Holthus, Clinical Recruiter at 734-259-9375 or Envision Physician Services is a dynamic physician- and clinician-led medical group that has been offering exceptional career opportunities for more than 60 years. With our national network of clinicians who are committed to delivering high-quality care, Envision Physician Services is nationally recognized for delivering clinical excellence supported by innovation, integration and exceptional leadership. Candidates considering becoming a teammate at Envision Physician Services will find full-time, part-time and independent contractor opportunities available in a variety of community types, from rural and underserved communities to major metropolitan areas; practice settings, from small hospitals to academic health systems; and job levels, from entry level to senior management. Envision teammates also benefit from the following resources: \t • Strong leadership at local, regional and national levels\t, • Exceptional quality of practice backed by comprehensive support services\t, • Optimal care teams with flexible and equitable scheduling options\t, • A-rated professional liability insurance\t, • Extensive variety of practice settings coast-to-coast\t, • Competitive compensation, including several benefit options\t, • Opportunities for professional development, mentoring and career advancement\t, • Clinician mental health and well-being support\t, • Comprehensive education and training on leadership, management and clinical best practices, including a wide variety of CME programs\t, • Clinical and scientific research opportunities *Benefits vary by division, clinical specialty and employment status.

New Increased Compensation!! Incredible CAA Opportunity, $75K Start Date Bonus-Come join our growing team at Baptist Hospital in Miami, FL!! Envision Physician Services is seeking a CAA to join the highly regarded practice of anesthesia services for Baptist Hospital of Miami, FL! Practice Highlights: * Care Team Model of 32 Anesthesiologists and 58 Allied Health, both CRNAs and CAAs. * Broad case mix including, but not limited to, Neuro, Vascular, General, OB/Gen, Ortho, IR, GI, Cardiac, Interventional Cardiac and Pedi. * Annual case volume of 40K * Team covers main hospital, 24 OR's, in addition to ASCs and a number of offsite locations. * No call with flexible scheduling options of 8's, 10's and 12's. * We offer a robust orientation/onboarding program for new hires; New grads are welcome to apply! * Benefits eligible day one of employment- No waiting period! * Company pays 100% of professional liability insurance with tail coverage. For more information about this opportunity, please contact Maryann Holthus, Clinical Recruiter at 734-259-9375 or Envision Physician Services is a dynamic physician- and clinician-led medical group that has been offering exceptional career opportunities for more than 60 years. With our national network of clinicians who are committed to delivering high-quality care, Envision Physician Services is nationally recognized for delivering clinical excellence supported by innovation, integration and exceptional leadership. Candidates considering becoming a teammate at Envision Physician Services will find full-time, part-time and independent contractor opportunities available in a variety of community types, from rural and underserved communities to major metropolitan areas; practice settings, from small hospitals to academic health systems; and job levels, from entry level to senior management. Envision teammates also benefit from the following resources: \t • Strong leadership at local, regional and national levels\t, • Exceptional quality of practice backed by comprehensive support services\t, • Optimal care teams with flexible and equitable scheduling options\t, • A-rated professional liability insurance\t, • Extensive variety of practice settings coast-to-coast\t, • Competitive compensation, including several benefit options\t, • Opportunities for professional development, mentoring and career advancement\t, • Clinician mental health and well-being support\t, • Comprehensive education and training on leadership, management and clinical best practices, including a wide variety of CME programs\t, • Clinical and scientific research opportunities *Benefits vary by division, clinical specialty and employment status.

The Department of Obstetrics, Gynecology & Reproductive Sciences, Division of OB/GYN Generalist has an exciting opportunity for an Assistant Professor of Clinical. The faculty will have clinical responsibilities within the Department of Obstetrics, Gynecology & Reproductive Sciences. The incumbent will serve as an attending physician in the Division of Ob/Gyn Generalists, with focus on the care and treatment of obstetric patients. This includes inpatient attending responsibilities for the division on inpatient units at Jackson Holtz Womens & Childrens Hospital Core Job Functions: Members of the Ob/Gyn Generalists Division provide comprehensive obstetric & gynecologic care to women working alongside allied health professionals, specialists and subspecialists in both the University of Miami/ UHealth and Jackson Health Systems. Primary duties will include: * Active participation in the inpatient and outpatient clinical practice of Obstetrics and Gynecology at the Jackson South Medical Center. * Participation in the advancement and education of OB/GYN medical students, residents, and fellows.?? * Develops and carries out a comprehensive medical treatment plan addressing biological, psychological, and sociocultural domains. * Performs physical assessment of patients in a logical and respectful manner. Prescribes medical treatment and clinical drugs to patients. * Gathers essential and accurate information through the review of pertinent records and interviews with the patient, family members, caregivers, and other health professionals. Reports to the responsible physician and complies with policy co-sig. * Reports hazardous or unsafe conditions, equipment malfunction, and supply instrumentation inadequacies to appropriate personnel. * Reports all Quality Assurance (QA) incidences, including mediation errors, to responsible physician using department guidelines. * Assumes responsibility for increasing knowledge and expertise by attending continuing educational offerings. * Makes informed decisions about interventions based on patient information and preference, up-to-date scientific evidence in the field, and clinical judgment. * Maintains confidentiality of all patient information according to federal and state guidelines and regulations. * Adheres to University and unit-level policies and procedures and safeguards University assets. Core Qualifications: Education: * Board Certified/Board Eligible in Obstetrics & Gynecology Certification and Licensing: * Certification in relevant specialty or field required * Active Florida Medical License & DEA * Credentialing needed Experience: * Minimum of 2 years of experience. Minimum Requirements: * Candidates should have a MD/DO and be BE/BC in Obstetrics & Gynecology * Must hold or be eligible for a full, unrestricted Florida Medical license. Knowledge, Skills and Attitudes: * Ability to maintain effective interpersonal relationships. * Ability to work independently and/or in a collaborative environment. * Ability to analyze, organize and prioritize work under pressure while meeting deadlines. * Ability to process and handle confidential information with discretion. * Ability to work evenings, nights, and weekends?as necessary. * Commitment to the Universitys core values. Department Specific Functions Members of the Generalist Division provide comprehensive obstetrical and gynecologic care to women working alongside allied health professionals, specialists and subspecialists in both the University of Miami/ UHealth and Jackson Health Systems. Specialty care includes uterine fibroids, sexual health, pelvic pain, vulvar abnormalities, family planning, preconception counseling, cervical dysplasia, and anal dysplasia. A strong commitment to teaching medical students, residents and fellows, and conducting research are prerequisites for leading the Generalist Division in the role as Division Chief. Clinical investigation includes a broad range of domains, including but not limited to patient oriented, translational, epidemiologic, behavioral, outcomes, implementation or health services research. In addition, faculty will have the opportunity for daily interaction and teaching to our 28 residents and medical students. All candidates should be dedicated to providing high quality patient care and exemplary teaching. The department is composed of 30+ faculty members and is based at the University of Miami/ UHealth and Jackson Health Systems in Miami, which is easily accessible and centrally located in Miami, Florida. The Jackson Memorial Holtz Womens & Childrens Hospital averages 4,000 deliveries a year and has a level 3 NICU staffed by UHealth neonatologists. The Womens Hospital at Jackson Memorial has been recognized by the Maternal Safety Foundation as an Accreta Center of Excellence and as VBAC Center of Excellence. Additional responsibilities: * Outpatient clinics. * Direct care to OB/GYN patients. * Consultation for hospitalized patients on L&D service. * Consultation for nonservice unit patients by telephone. * Inpatient L&D at Jackson Holtz Womens & Childrens Hospital * Required to cover 12 hours shifts on L&D, 6 shifts per month * Will need to use EPIC at UHealth Clinics & Cerner at Jackson Health for documentation and MobileCharge for billing

CRNA Opportunity! How would you like to join an EXCELLENT TEAM !! Envision Physician Services and Aventura Hospital are currently seeking CRNAs to join our collaborative Anesthesia team located in the Miami area! * Team is comprised of 13 physicians and 14 APP's * Facility consists of 1 main hospital * Approximately 11,000 annual cases.11 OR's, 3 Endo, 3 Cath Labs * Case mix includes Neuro, Orthopedics, ENT, Urology, GI, Cardiovascular, Urology and extensive General Surgery * No Peds. No OB * APP's place lines, manage meds and do blocks * Flexible scheduling opportunities include 8's, 10's, 12-hour shifts * Call requirements: 1:5 weekends * Opportunity to make more if you want * PTO increased to 8 & 9 weeks * CME allowance * Medical, dental, vision, short-term/long-term disability, 401(k) contribution, health savings + more! * Malpractice provided For more information about this opportunity, please contact Maryann Holthus, Clinical Recruiter at 734-259-9375 or Envision Physician Services is a dynamic physician- and clinician-led medical group that has been offering exceptional career opportunities for more than 60 years. With our national network of clinicians who are committed to delivering high-quality care, Envision Physician Services is nationally recognized for delivering clinical excellence supported by innovation, integration and exceptional leadership. Candidates considering becoming a teammate at Envision Physician Services will find full-time, part-time and independent contractor opportunities available in a variety of community types, from rural and underserved communities to major metropolitan areas; practice settings, from small hospitals to academic health systems; and job levels, from entry level to senior management. Envision teammates also benefit from the following resources: \t • Strong leadership at local, regional and national levels\t, • Exceptional quality of practice backed by comprehensive support services\t, • Optimal care teams with flexible and equitable scheduling options\t, • A-rated professional liability insurance\t, • Extensive variety of practice settings coast-to-coast\t, • Competitive compensation, including several benefit options\t, • Opportunities for professional development, mentoring and career advancement\t, • Clinician mental health and well-being support\t, • Comprehensive education and training on leadership, management and clinical best practices, including a wide variety of CME programs\t, • Clinical and scientific research opportunities *Benefits vary by division, clinical specialty and employment status.

The Division of Nuclear Medicine in the Department of Radiology at the University of Miami Miller School of Medicine is seeking to fill a full-time faculty position at the rank of Division Director Associate and/or Professor level (Dual Boarded). The Division Director of Nuclear Medicine will be responsible for leading and supervising the clinical operation and academic functions of the Nuclear Medicine Division within Radiology Department at the University of Miami Miller School of Medicine (UMSOM) and Jackson Health Services (JHS). The successful candidate will be tasked with ensuring that the Division maintains a highly competitive status within a top-tier institution. Facility resources include a state-of-the-art PET/CT, SPECT/CT and gamma camera equipment, with associated computer hardware and software for dedicated nuclear medicine post-processing and advanced analysis. Newer additions include capabilities for Artificial Intelligence integration into the workflow. Job Functions * Provide clinical oversight and leadership to the nuclear medicine division, including study interpretation. * Lead the growth and expansion of the nuclear medicine clinical operation and services across UHealth. * Manage/develop a team of physicians, residents/fellows, technologists, and support staff (e.g. hiring, training, evaluating performance). This includes proposing mentorship and research initiatives. * Ensure regulatory and accreditation compliance, including maintaining appropriate licensure and certification. * Coordinate with faculty/staff and departmental leadership to streamline patient care and operational efficiency. * Develop and implement clinical programs to ensure the highest level of patient care and safety. * Foster a culture of excellence by promoting professional development, research, and superior education. * Participate in quality improvement initiatives to improve patient outcomes and operational efficiency. * Collaborate with other healthcare providers and stakeholders to ensure effective coordination of care. * Manage and coordinate Nuclear Medicine therapies across UHealths system, such as multidisciplinary workups and therapies in the realm of Theranostics, including experimental treatments. * Multidisciplinary collaboration for clinical and innovation initiatives with other departments, such as: Medical Oncology, Cardiology, Radiation Oncology, Endocrinology, and others to foster common approaches. * Successfully lead the Division of Nuclear Medicine in supporting the departmental and institutional objectives for excellence in the arenas of: clinical, teaching and education, research, administration, service, citizenship. * Responsibilities of the candidate include providing interpretations of plain film, CT and MR studies, from multiple facilities, including Jackson Memorial Hospital. * Provide clinical care/consultation, teaching of trainees, service, and potential involvement in research. * Participation in grand rounds, journal clubs, multidisciplinary conferences. Able to serve on departmental and institutional committees. * Recruiting, training, and mentoring other faculty and staff physicians. * Conducting research and publishing papers in academic journals. * Representing the university at conferences and delivering presentations when necessary. * Teaching and supervising undergraduate and graduate students * Attending faculty and departmental meetings and voicing concerns or providing suggestions for improvement. Qualifications * Medical Doctor degree and board certification in both Diagnostic Radiology (ABR) and Nuclear Medicine (ABNM). Dual Boarded. * Academic rank of Associate or Full Professor. * Minimum of 7 years of experience in nuclear medicine interpretation and reporting. * Experience in managing a team of physicians, scientists, residents/fellows, technologists, and support staff. * Knowledge of regulatory requirements and accreditation standards related to nuclear medicine. * Strong communication and collaboration skills. Track record of multidisciplinary research. * Demonstrated commitment to high quality patient care and safety. A track record of developing tailored diagnostic and therapeutic nuclear medicine regimens in complex clinical scenarios will be noted. * Ability to think critically, solve complex problems, and to interact and communicate effectively. * Experience with clinical program development and implementation. * Expertise in the interpretation and reporting of nuclear medicine studies, as well as experience in managing a team of physicians, scientists, residents/fellows, technologists, and support staff. * Excellent nuclear medicine background with working experience in all facets of nuclear medicine, molecular imaging and radiopharmaceutical therapies. * A vision in the burgeoning realm of Theranostics is highly desired, which the candidate should be prepared to articulate. * Resident/Fellow education and training in nuclear medicine is another critical aspect. . * Experience in Radiopharmaceutical Therapy and Theranostics is highly desired as the Division is quite active in conventional and new therapies for thyroid cancer, lymphoma, neuroendocrine tumors, and prostate cancer, to name a few. * Excellence in academic achievement as demonstrated by a record of scientific presentation and/or publications. The successful applicant will join a group of six Nuclear Medicine Radiologists who practice at Jackson Memorial Hospital and the University of Miami Hospital and Clinics. Jackson and UHealth deliver leading-edge care by the regions top doctors, powered by the groundbreaking research of the University of Miami Miller School of Medicine. As South Floridas only University-based comprehensive Health system, UHealth is a vital component of the community that is leading the next generation of health care.

Job Requisition: Clinical Research & Evidence Manager Company: Rho Nutrition Location: United States (Remote) Employment Type: Full-Time Reports To: VP of Science & Innovation About Rho Nutrition Rho Nutrition is a fast-growing, science-driven CPG company redefining the supplement industry through liquid, liposomal delivery technology. Operating across Shopify DTC, Amazon, and national retail, Rho serves hundreds of thousands of customers and is scaling rapidly while maintaining strict standards around quality, transparency, and scientific rigor. Role Overview Rho Nutrition is seeking a Clinical Research & Evidence Manager to support the execution, organization, and application of our clinical research initiatives. This role will oversee external research partnerships and clinical studies while ensuring scientific evidence is clearly documented, maintained, and accessible to support internal decision-making across product development, education, and growth. The ideal candidate brings strong experience in clinical or applied research environments, is comfortable working with external research partners, and can translate complex study outputs into clear, structured insights for cross-functional teams. This role plays a key part in ensuring Rho’s scientific foundation continues to scale alongside the business. Key Responsibilities • Manage and coordinate clinical research initiatives, including observational studies, interventional trials, and PK or exploratory research, • Serve as the primary point of contact for external research partners, CROs, and study vendors, • Support IRB submissions, protocol updates, amendments, and study close-outs as needed, • Track study timelines, milestones, endpoints, and operational risks, • Organize and synthesize study outputs into clear internal scientific summaries and executive-level briefs, • Maintain structured evidence libraries organized by product, ingredient, and outcome, • Support internal teams by clarifying existing evidence and appropriate scientific context, • Partner cross-functionally with Product, Education, Marketing, and CX teams to ensure scientific information is accurately reflected across materials, • Identify emerging research needs as the product portfolio and business evolve, • Escalate ambiguous findings or limitations with clear context and recommendationsQualifications & Experience, • Advanced degree in a relevant scientific or clinical field (MS, MPH, PharmD, or equivalent), • 3+ years of experience in clinical research, translational science, or applied research environments, • Hands-on experience working with clinical studies, research platforms, or CROs, • Strong ability to synthesize scientific data into clear, structured insights, • Experience operating in fast-paced, cross-functional environments Preferred: • PhD or professional degree in a relevant discipline, • Experience in nutrition, dietary supplements, or consumer health products, • Familiarity with applied research in commercial or regulated settings What Success Looks Like in This Role • Clinical research initiatives are well-organized, on track, and clearly documented, • Internal teams have clear visibility into available scientific evidence, • Study outputs are translated into usable insights for product, education, and planning, • Reduced ad hoc scientific questions routed to senior leadership, • Strong, productive relationships with external research partnersWhy Join Rho Nutrition, • Join a founder-led, science-driven brand at a critical growth stage, • Work remotely with a highly collaborative, high-caliber leadership team, • Play a meaningful role in shaping how scientific evidence supports a fast-scaling product portfolio, • Competitive compensation and long-term growth opportunities

CRA II local/very regional travel US, Clinical Research Associate, Sponsor Dedicated ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Research Associate II in Miami, FL to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials., • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process., • Collaborating with investigators and site staff to facilitate smooth study conduct., • Performing data review and resolution of queries to maintain high-quality clinical data., • Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your profile • Bachelor's degree in a scientific or healthcare-related field., • Minimum of 2 years of experience as a Clinical Research Associate., • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines., • Strong organizational and communication skills, with attention to detail., • Ability to work independently and collaboratively in a fast-paced environment., • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

Job DescriptionThe Opportunity: Patent Agent Job SummaryA nationally recognized law firm is seeking an experienced Patent Agent to join its dynamic Intellectual Property (IP) team. The ideal candidate will have a strong background in life sciences, possess a Ph.D. in a related field, and have at least five (5) years of experience in patent prosecution. This is an excellent opportunity to work with a highly respected team handling complex patent matters for a diverse range of clients, from biotech startups to multinational pharmaceutical and biotechnology companies.Job Description • Prepare, draft, and prosecute U.S. and international patent applications in the life sciences sector, including biotechnology, pharmaceuticals, and related disciplines., • Conduct patentability assessments, freedom-to-operate analyses, and due diligence reviews to support client business strategies., • Collaborate closely with inventors, scientists, and legal teams to develop strong patent portfolios that align with clients' research and commercialization goals., • Assist in IP strategy development, portfolio management, and competitive landscape analysis for clients in the biotechnology and pharmaceutical industries., • Monitor industry trends, scientific advancements, and regulatory developments to provide informed legal guidance to clients., • Work with attorneys on IP litigation support, post-grant proceedings, and opinion work, including validity and infringement analyses., • Communicate effectively with the U.S. Patent and Trademark Office (USPTO) and foreign patent offices regarding patent prosecution matters.Required Qualifications, • Ph.D. in Life Sciences (e.g., Molecular Biology, Biochemistry, Genetics, Immunology, Microbiology, or a related field) is required., • Minimum of 5 years of experience in patent prosecution, preferably in a law firm or corporate setting., • Exposure to IP due diligence, licensing, and transactional work., • Familiarity with post-grant proceedings, including IPRs and oppositions., • Registered to practice before the U.S. Patent and Trademark Office (USPTO)., • Strong understanding of U.S. and international patent laws, regulations, and procedures., • Excellent technical writing and analytical skills with a keen attention to detail., • Ability to work independently and collaboratively in a fast-paced, client-focused environment., • Strong verbal and written communication skills for interacting with clients, attorneys, and technical professionals.

Job DescriptionAbout MMS Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research. Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit or follow MMS on LinkedIn. Applicants must be legally authorized to work in the U.S. for any employer; we cannot sponsor visas (e.g., H-1B) or offer work authorization transfers at this time. Job Specific Skills: • Mastery and trained on generating tables, listings, and graphs from clinical trial databases using SAS., • Utilizes System Development Life Cycle (SDLC) for programming deliverables., • Advanced user in SAS programming, SAS Base, and SAS Macros., • Advanced knowledge of E-Submission Standards, Guidelines and Regulations., • Mastery and trained on SDTM standards including ability to write specifications., • Advanced knowledge of ADaM standards including supporting specification writing., • Proficient with MS Office applications., • Advanced knowledge of ICH, 21CRF Part 11, and ISO 9001:2000 requirements., • Advanced experience with pooling of data sets for submissions., • Advanced experience with BIMO outputs, define.xml, Reviewer's Guides, SDSP., • Lead study or small programming project teams.Job Requirements:, • Masters required for all Statistics roles., • Minimum of 5 years’ experience in Statistical Programming or similar field required., • Expert knowledge of scientific principles and concepts., • Reputation as emerging leader in field with sustained performance and accomplishment., • Proficiency with MS Office applications., • Hands-on experience with clinical trial and pharmaceutical development preferred., • Good communication skills and willingness to work with others to clearly understand needs and solve problems., • Excellent problem-solving skills., • Good organizational and communication skills., • Familiarity with current ISO 9001 and ISO 27001 standards preferred., • Familiarity with 21 CFR Part 11, FDA, and GCP requirements. P9JqgBb4IE

Job DescriptionBenefits: • 401(k), • 401(k) matching, • Dental insurance, • Employee discounts, • Flexible schedule, • Health insurance, • Paid time off As a BDR, you will report directly to the Director of Sales and work closely with the CEO, VP of Sales, and VPs of Technical Services, gaining unparalleled exposure to cybersecurity expertise and sales mastery. This role is ideal for candidates eager to hone their skills in sales methodologies like Gap Selling and The Challenger Sale and expand their ability to qualify prospects and engage in strategic business conversations beyond technical security topics. Responsibilities • Execute high-volume outbound prospecting via cold calls, emails, and social media to generate qualified meetings with decision-makers in regulated industries (healthcare, energy, banking, critical infrastructure)., • Achieve a goal of booking 1822 qualified meetings per month by Month 4, embracing a one more call, one more meeting mentality to exceed targets., • Learn and articulate InfoSights core offerings, including penetration testing, compliance assessments, fractional vCISO, and managed IT/OT security services., • Qualify prospects effectively during cold calls, identifying needs and aligning them with appropriate solutions, while developing the ability to lead broader business conversations., • Leverage sales enablement tools including Orum, SalesLoft, SalesNav, ZoomInfo, Salesforce, and others for research, outreach, and pipeline management., • Maintain accurate and timely records in Salesforce, ensuring strong CRM hygiene., • Participate in weekly coaching, call reviews, live call shadowing, and structured training on products, industry trends, and sales methodologies (e.g., Gap Selling, Sales EQ, Challenger Sale)., • Stay current on cybersecurity trends, solutions, pricing models, and regulatory frameworks (e.g., PCI-DSS, GLBA, HIPAA)., • Collaborate with senior leadership to refine outreach strategies and develop strategic alignment with key third-party influencers.Qualifications, • Required: 1+ year of B2B outbound sales experience (BDR, SDR, inside sales, or AE)., • Strongly Preferred: Knowledge of cybersecurity, particularly in OT (Operational Technology) cybersecurity or SLED (State, Local, and Education) markets., • Proven success with high-volume cold calling and outbound prospecting., • Excellent verbal and written communication skills, with the ability to quickly learn technical subject matter and engage in strategic business discussions., • Strong organizational skills and attention to CRM/process discipline., • Competitive, coachable mindset with a one more mentality and eagerness to exceed goals., • Interest in mastering sales methodologies (e.g., Gap Selling, Sales EQ) through training and self-study., • Exceptional computer skills, including proficiency with Salesforce, Microsoft Office Suite, and web presentation tools., • Ability to manage multiple tasks in a fast-paced, remote environment with a strong work ethic and sense of urgency., • Preferred: Bachelors degree in cybersecurity, IT, or a related field., • Bonus: Experience in IT services, SaaS, or consulting/advisory services; background in athletics, military, or other competitive environments; understanding of regulatory compliance frameworks (e.g., PCI-DSS, GLBA, HIPAA, NERC-CIP) or risk management/governance.How You Stand Out, • Significant B2B sales experience with a track record of over-achieving quotas., • Mastery of the cybersecurity narrative, particularly in MSSP/SOCaaS, threat management, or penetration/vulnerability testing., • Thorough understanding of managed security solutions and experience working with an MSSP., • Strong prospect qualification skills during cold calls, with the potential to expand into broader business conversations., • Proficiency with corporate productivity tools and a scientific approach to sales processes., • Strong knowledge of current cybersecurity threats and news. This is a remote position.

Job Description Location: This role is onsite at CPMI in Miami, FL If you are not local to Miami, let's discuss how to get you there! This is a newly created role at an amazing, top clinical research site located in Miami, FL About Company: Who is ERG? ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with an expertise in early and late-stage neuroscience drug development. With 19 wholly owned clinical sites and 5 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies. ERG has 340+ in-patient beds, a large and growing database of patients suffering from mental illness, neurological disorders, sleep disorders, addictions, Acute and Chronic Pain, diabetes and other illnesses as well as normal healthy volunteers who participate in trials for the advancement of medicine. With access to over 32 million patients/subjects and 5000 + completed trials, ERG continues to grow its capabilities and expand into indications where there are tremendous unmet medical needs in the United States and globally. About the Role: We are seeking a highly qualified Manager/Director of Clinical Operations, Phase I, to oversee clinical trials, ensuring protocol adherence, and managing both staff and operational aspects of studies. This role demands strict compliance with GCP, ICH guidelines, and company SOPs. Core duties include staff management, protocol review, quality assurance, and overall study supervision. Responsibilities: • Lead and mentor the clinical operations team to promote a collaborative and efficient environment., • Ensure protocol compliance and maintain high-quality standards across studies., • Collaborate closely with Principal Investigators and Site Directors to assign studies and develop enrollment strategies., • Oversee human resources functions, including staff evaluations, recruitment, and training., • Monitor adherence to protocols, reporting any deviations to sponsors and regulatory bodies., • Coordinate with Site Director and Principal Investigator to assign primary clinical research coordinators., • Review study components with Principal Investigators and Site Directors, identifying areas requiring clarification before study initiation., • Conduct study closeout procedures., • Perform additional duties as needed to adapt to the evolving needs of CPMI., • Bachelor's degree in a scientific or healthcare-related field, • 7-10 years of experience in clinical operations, including 5+ years in a senior leadership role., • Strong understanding of FDA, ICH, and GCP regulations and guidelines, • Strong communication, organizational, and leadership skills., • Ability to travel as needed and proficiency in Microsoft Word, Excel, and clinical management software., • In-depth knowledge of clinical trial operations, including study start-up, site selection, patient recruitment, monitoring, data management, and study close-out, • Phase I or early phase experience Our comprehensive benefits package includes: • Health insurance, • Dental & Vision Insurance, • Matching 401k Retirement Plan, • Paid Time Off (PTO)

Job Description Empower, Innovate, Impact! At Team A-TEK, we EMPOWER people to drive INNOVATION that IMPACTS mission! A-TEK operates at the intersection of mission and innovation by applying our deep domain expertise across the federal markets. Embracing our digital-first strategy, A-TEK provides enhanced capabilities in application development, digital transformation, enterprise IT, and scientific services. Our solutions are designed to modernize, automate, secure, protect, and enhance the operations of our federal clients, ensuring they stay ahead in a rapidly evolving digital landscape. Our work is fueled by a passion to serve our clients' needs and to protect the safety and welfare of Americans. That passion shapes how we nurture our most valuable asset – Our Employees. A-TEK actively cultivates the talent that drives our success and fosters a creative, challenging, and mission-driven work environment for current and future employees. This position will be responsible for performing non-research molecular testing of samples for potentially containing biological threat agents. Ensures incoming operational, QA, and other sample types are processed while maintaining chain of custody. Prepares reports, answers questions, troubleshoots, and makes recommendations to the supervisor for inclusion in comprehensive reports. Maintains and operates equipment properly and in a safe manner, including performing routine calibrations and adjustments. Performs all procedures in accordance with proper handling and storage of various materials. Additionally, will be responsible for maintaining knowledge and skills related to position and program. Laboratory operations are 7 days a week. Team members take turns with weekends and holidays to ensure results are reported each day. In the event of a public health emergency, extended work hours and alternative shift work may be required to maintain temporary emergency 24/7 operations. Kindly be aware that a pre-employment drug screening is a requirement. REQUIRED QUALIFICATIONS: Bachelor's degree from an accredited university in microbiology, molecular biology, or related course work in biological sciences. REQUIRES at least one year of laboratory bench experience, utilizing PCR, aseptic techniques and experience with biological assays. Laboratory training that is assigned or accompanies an associated course is not considered applicable training This position supports a federal contract which requires that all employees and job applicants hold a valid Green Card or US Citizenship at the time of application. Candidates may use tools (including AI) for proofreading or formatting; however, using any tool to fabricate, exaggerate, or misrepresent qualifications, experience, or work product is not permitted. We may assess application materials for job-related technical depth, internal consistency, and demonstrated hands-on experience, including through follow-up questions, skills assessments, or reference checks. Misrepresentation or falsification may result in removal from further consideration. Candidates who need a reasonable accommodation in the application or interview process may request one. A-TEK, Inc. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or status as a qualified individual with a disability, or Vietnam era or other protected Veteran status. Verification of education may be requested before or during the hiring process.

Job DescriptionWe are currently partnering with an established clinical research client in the Miami area looking to add a dedicated Pharmacist to their team. This is a specialized role designed for a clinician who excels in high-precision environments and is passionate about the future of medicine through clinical investigational drug trials. Position Overview As a Clinical Research Pharmacist, you will work at the intersection of patient care and scientific innovation. You will collaborate closely with Principal Investigators, the Director of Operations, and internal research staff to manage the lifecycle of investigational medications. Your primary focus will be ensuring strict protocol compliance, meticulous inventory management, and the safe preparation of study materials. Key Responsibilities Clinical Preparation: Perform complex dilution ratios, set up IV bags, and prepare subcutaneous injections with high accuracy. Specialized Handling: Manage field mixing for vaccine studies and oversee the precise counting and dispensing of oral medications. Protocol Implementation: Review investigational drug trial protocols and implement required pharmacy procedures to ensure 100% compliance. Inventory Management: Lead the ordering, replacement, and return of all study-specific materials and maintain up-to-date investigational drug lists. Cross-Functional Collaboration: Partner with Principal Investigators and coordinators to define compounding and dispensing processes for each unique trial. Quality & Compliance: Monitor daily pharmacy activities to ensure adherence to dispensing procedures, inventory documentation, and billing requirements; report any ethical concerns or protocol deviations. Documentation: Maintain comprehensive pharmacy binders for each trial, including study summaries, checklists, and required regulatory documentation. Education, Training, and Collaboration Staff Mentorship: Train and orient pharmacy staff and residents on investigational drug trial procedures and specific pharmacy roles. Consultation: Serve as the subject matter expert on drug information for physicians, nurses, and other healthcare professionals. Professional Growth: Attend interdisciplinary team meetings and participate in committees, educational rounds, and journal clubs to stay current with best practices. Required Qualifications Education: Doctor of Pharmacy (PharmD) degree from an accredited program. Licensure: Active and unrestricted Florida Pharmacy License. Technical Proficiency: Demonstrated experience in IV compounding, dilution calculations, and subcutaneous medication preparation. Attributes: Exceptional attention to detail, strong ethical judgment, and the ability to work in a fast-paced, protocol-driven environment. Equal Opportunity Employer / Disabled / Protected Veterans The Know Your Rights poster is available here: The pay transparency policy is available here: For temporary assignments lasting 13 weeks or longer, the Company is pleased to offer major medical, dental, vision, 401k and any statutory sick pay where required. We are committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation for any part of the employment process, please contact your staffing representative who will reach out to our HR team. AppleOne participates in the E-Verify program in certain locations as required by law. Learn more about the E-Verify program. We also consider for employment qualified applicants regardless of criminal histories, consistent with legal requirements, including, if applicable, the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records, including, if applicable, the San Francisco Fair Chance Ordinance. For Los Angeles, CA applicants: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. #1171 Company DescriptionThis company offers growth and a great group of people to work with.This company offers growth and a great group of people to work with.

Job Description Show off your talent and join our team! POSITION SUMMARY: The Digital Media Creator has expertise in videography, video creation, and video editing, along with a strong background in social media management and digital asset creation. The ideal candidate will be responsible for planning, creating, executing, and managing multimedia campaigns to engage audiences and enhance brand visibility. This includes creating compelling video content, managing social media platforms, and supporting other digital marketing tasks. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. SUPERVISION RECEIVED AND EXERCISED: Receives direct supervision from Director of Marketing. May assist other departmental employees in the performance of the job functions. Does not supervise other position(s). This position is located in Building 3 - Marketing Department. DUTIES AND RESPONSIBILITIES: • Videography & Video Creation: Plan, shoot, and edit high-quality videos for marketing campaigns, social media, product promotions, and more., • Video Editing: Use industry-standard editing software to create compelling video content, including promotional videos, product demos, event recaps, and tutorials., • Social Media Content Creation: Develop engaging digital assets for social media platforms, ensuring consistency with brand messaging and visuals., • Social Media Management: Execute and manage content schedules across multiple social media channels (Facebook, Instagram, LinkedIn, YouTube, etc.), optimizing engagement and reach., • Paid Media Campaigns: Plan and execute paid media campaigns across platforms such as Google Ads, YouTube Ads, and Linkedin, ensuring video content is optimized for each medium., • Collaborate with Design Teams: Work with graphic designers and marketing teams to develop visual assets and ensure video content aligns with campaign goals., • Lead Generation & Digital Marketing: Develop video content and digital assets to drive leads, support email campaigns, and optimize performance for SEO and SEM., • Market Research: Analyze target audiences to develop video strategies that resonate with key demographics., • Digital Advertising: Oversee video ads and digital asset performance, adjusting campaigns based on metrics to maximize ROI., • CRM & Analytics: Manage lead data in CRM systems and track digital asset performance with analytics tools., • Additional Duties: Assist with other digital media needs as required, including photo shoots, website content updates, and digital asset organization. QUALIFICATIONS/REQUIREMENTS: • Bachelor Degree in Marketing, Communications or a related field., • 2 to 4 years of hands-on experience in videography, video editing, and social media content creation., • Proficient in video editing software such as Adobe Premiere Pro, Final Cut Pro, or similar., • Experience with digital asset creation: Graphic design knowledge and proficiency in tools like Adobe Creative Suite (Photoshop, Illustrator) is a plus., • Experience with paid media (Google Ads, Facebook Ads, LinkedIn Ads, YouTube, etc.) and social media advertising platforms., • Knowledge of SEO and SEM strategies to enhance video content visibility., • Excellent project management skills: Ability to manage multiple projects simultaneously while meeting deadlines., • Strong communication skills: Ability to collaborate with cross-functional teams and stakeholders., • Ability to adapt and thrive in a fast-paced environment with shifting priorities and deadlines., • Strong analytical and data-driven mindset to evaluate video and campaign performance., • Must be fluent in English (reading/writing); Fluency in Spanish is a plus., • Must be open to potential travel as needed., • Must submit a portfolio for review to assess the quality of video work. PHYSICAL/MENTAL REQUIREMENTS: • High energy level, comfortable performing multifaceted projects in conjunction with normal activities., • While performing the duties of this job, the employee is regularly required to sit and use their fingers., • The employee frequently is required to talk and/or hear., • The employee is occasionally required to sit, stand and walk., • The employee must occasionally lift and/or move up to 20 pounds., • Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus., • Ability to define problems, collect data, establish facts, and draw valid conclusions., • Ability to exercise independent judgment within established systems and procedures., • Strong organization and time management skills., • Ability to communicate (read and write) effectively in a business environment. WHAT YOU'LL GET WHEN YOU JOIN THE GAUMARD FAMILY: • Competitive Pay., • Full health benefits (medical, vision, dental)., • Paid Time Off (PTO)., • 11 Paid Holidays., • Retirement plan with 100% employer match up to 5% of employee's contribution., • Satisfaction knowing that you have joined a long-standing company. Hours: Monday to Friday 8:00 AM to 4:30 PM must be willing and able to work some Saturdays or stay beyond scheduled shift if needed to meet business demands. The above job description supersedes all previous descriptions. This job description is intended to be a tool to describe the primary purpose of the job and the KEY duties and responsibilities. This description does not state or imply that the functions listed above are the only tasks to be performed by the employee occupying this position. Management has the right to add to or change the job responsibilities at any time. Equal Employment Opportunity Statement: Gaumard Scientific is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: Gaumard Scientific is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Gaumard Scientific are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Gaumard Scientific will not tolerate discrimination or harassment based on any of these characteristics. Gaumard Scientific encourages applicants of all ages. Gaumard Scientific will provide reasonable accommodation to employees who have protected disabilities consistent with local law.

Job DescriptionAre you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research. Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit or follow MMS on LinkedIn. As part of our Strategic Statistical Services Arm, this is a full-time role with emphasis on being an internal and external SME for clinical trial design, together with providing consultation to advise clients on a range of broader statistical issues, and will have an internal job title of Strategic Statistician. Job Description: Our experienced statisticians and programmers develop intellectual property and assets to support the design and analysis of clinical trials, precision medicine and real-world data analytics. We address the emerging analytics needs of the Industry with our biostatistics services, bespoke algorithms and unique, state of the art, proprietary, cloud-based trial simulation software KerusCloud. Working alongside innovative statisticians you will be responsible for leading the full life-cycle of KerusCloud support and statistical services, from: • Assisting customers with their study design with a particular focus on simulation with KerusCloud to ensure they are aligned with the study objectives., • Preparation of study protocols and development of Statistical Analysis Plans and Statistical Analysis Reports., • Summarize, analyze and visualize study data using a variety of statistical methods, ultimately delivering results to an agreed timeline with optimal quality., • Provide statistical consultancy support to sponsors across the full span of clinical development, including oversight of third-party statistical and programming deliverables., • Maintain current knowledge of relevant research techniques such as modelling, simulation and experimental design and participate in continuous professional development activity., • Support pre-sales discussions to understand and identify client needs, then contribute to technical solutions and resource/ cost estimates., • Collaborate with the Product Development team defining key features and statistical aspects of KerusCloud., • Bachelors degree in mathematics, statistics, physics, pharmacology or with a strong statistical component, Masters or PhD preferred., • 5-7 years of experience in the application of medical statistics (pharma, CRO, academic)., • Willingness to engage with clients to understand and research problems and provide creative, business-orientated solutions., • Experience in delivering customer projects to high quality standards., • Experience in SAS and/ or R statistical software packages., • Experience in study design and protocol and report-writing preferred., • Experience of modelling and simulation techniques to explore complex study designs preferred., • Experience of Bayesian approaches to design and analysis of clinical data preferred. 1Gms7rTveP

Job Description Location: Menlo Park, CA / Miami, FL / Princeton, NJ ONSITE About Summit: Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit’s core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence. Summit’s team is inspired to touch and help change lives through Summit’s clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including: Non-small Cell Lung Cancer (NSCLC) * HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. * HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC. * HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC. Colorectal Cancer (CRC) * HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy. Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China’s National Medical Products Administration (NMPA). Summit is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland. Overview of Role: We are seeking a physician to serve as a Senior Medical Director to oversee global Phase 3 clinical trials a BLA (Biologic Licensing Application) filings. The incumbent will be primarily responsible for developing and executing an integrated clinical trial programs including protocol design and medical oversight of new or ongoing studies.? They will be responsible for obtaining scientific advisory input, work with biostatisticians for phase 3 design and analyses, support regulatory interactions for product advancement, and work closely with clinical operations to provide advice and decision making regarding medical input to achieve operational excellence.? The candidate must have demonstrated effective collaborative skills to work across various phases of clinical development and serve as a key medical expert for multiple cross functional teams.? This position will provide medical insight across a myriad of functions from discovery to manufacturing are expected.? Additionally, the Medical Director will play a pivotal role in leading investigator engagements including travel to support face-to-face interaction and protocol training.? Prior experience in a mid-sized, fast-growing pharmaceutical environment is preferred, as this role will be working on product development in an extremely fast-paced and intense environment.???The Medical Director will serve as a leader on one multiple potentially pivotal programs.? Role and Responsibilities: * Significant Oncology Experience the role will require expertise in the treatment and management of oncology disease such that knowledge can be applied to the strategy and clinical development of Summit medicines to benefit patients * Work cross functionally with Medical Affairs, Regulatory, Commercial and other functions to develop the overall product strategy in multiple indications * Work cross functionally with Clinical Operations, Biometrics, Pharmacovigilance, and other functions to successfully complete clinical development programs leading to BLA approvals * Lead teams to execute on clinical development goals (clinical trial execution, clinical development strategy, medical affairs planning) * Manage direct reports or cross functional team members as needed based on team needs * Contribute to the communication strategy of Summit products via publications, manuscripts, abstracts, posters and scientific presentations * Making vital contributions on pivotal programs in clinical development program? * Directing human clinical trials, phases 1-3, for lead candidate in development, helping to ensure all clinical development milestones are met including enrollment goals * Participating in medical review of adverse event reports and monitoring of incoming safety data in conjunction with product safety/pharmacovigilance, including evaluating and escalating safety signals? * Coordinate and develop information for reports submitted to FDA, EMA, PMDA, and government, regulatory, or partner agencies?? * Presentations to various external stakeholders - regulators, governing and harmonization bodies, principle investigators, scientific conference attendees, advisors and opinion leaders? * Knowledge of clinical trial conduct to support operational needs for planning and executing clinical trials, including adherence to protocols, safety reviews, assay development, training, and clinical document review? * Planning, reviewing and editing Clinical Study Reports? * Planning, reviewing and editing publications from the program * Providing input on the design of clinical studies supporting clinical strategy? * All other duties as assigned Experience, Education and Specialized Knowledge and Skills: * Board certified or eligible MD with hematology/oncology product development and experience across stages of clinical development? * Minimum of 5+ years’ experience in pharmaceutical, biologics, or biotech R&D environment, or in a research environment involving the collection and analysis of human data in the area of hematology/oncology * Working knowledge of clinical development pathways for hematology/oncology therapeutics in the US and EMA? * Self-starter who will move forward with key initiatives without being prompted, able to perform a myriad of tasks needed to support the clinical development program, possesses a highly entrepreneurial and growth mindset, works collaboratively with cross-functional teams, loves a good mission The pay range for this role is $283,000-$353,500 annually. Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation. Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Summit’s Talent Acquisition team at to obtain prior written authorization before referring any candidates to Summit.

The Department of Obstetrics, Gynecology & Reproductive Sciences, Division of OB/GYN Generalist has an exciting opportunity for an Assistant Professor of Clinical. The incumbent will serve as an attending physician in the Division of OB/GYN Generalists, with focus on the care and treatment of obstetric patients. This includes inpatient attending responsibilities for the division on inpatient units at Jackson Holtz Women’s & Children’s Hospital. CORE JOB FUNCTIONS Members of the Ob/Gyn Generalists Division provide comprehensive obstetric & gynecologic care to women working alongside allied health professionals, specialists and subspecialists in both the University of Miami/ UHealth and Jackson Health Systems. Primary duties will include: * Active participation in the inpatient and outpatient clinical practice of Obstetrics and Gynecology at the University of Miami Kendall Medical Center, Desai Sethi Institute, Doral Commons, University of Miami Hospital and Jackson Memorial Hospital. * Participation in the advancement and education of “OB/GYN” medical students, residents, and fellows.?? * Develops and carries out a comprehensive medical treatment plan addressing biological, psychological, and sociocultural domains. * Performs physical assessment of patients in a logical and respectful manner. Prescribes medical treatment and clinical drugs to patients. * Gathers essential and accurate information through the review of pertinent records and interviews with the patient, family members, caregivers, and other health professionals. Reports to the responsible physician and complies with policy co-sig. * Reports hazardous or unsafe conditions, equipment malfunction, and supply instrumentation inadequacies to appropriate personnel. * Reports all Quality Assurance (QA) incidences, including mediation errors, to responsible physician using department guidelines. * Assumes responsibility for increasing knowledge and expertise by attending continuing educational offerings. * Makes informed decisions about interventions based on patient information and preference, up-to-date scientific evidence in the field, and clinical judgment. * Maintains confidentiality of all patient information according to federal and state guidelines and regulations. * Adheres to University and unit-level policies and procedures and safeguards University assets. This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary. CORE QUALIFICATIONS Education: * Board Certified/Board Eligible in Obstetrics & Gynecology Certification and Licensing: * Certification in relevant specialty or field required * Active Florida Medical License & DEA * Credentialing needed Experience: * Minimum of 2 years of experience. Minimum Requirements: * Candidates should have a MD/DO and be BE/BC in Obstetrics & Gynecology * Must hold or be eligible for a full, unrestricted Florida Medical license. Knowledge, Skills and Attitudes: * Ability to maintain effective interpersonal relationships. * Ability to work independently and/or in a collaborative environment. * Ability to analyze, organize and prioritize work under pressure while meeting deadlines. * Ability to process and handle confidential information with discretion. * Ability to work evenings, nights, and weekends?as necessary. * Commitment to the University’s core values. Department Specific Functions Members of the Generalist Division provide comprehensive obstetrical and gynecologic care to women working alongside allied health professionals, specialists and subspecialists in both the University of Miami/ UHealth and Jackson Health Systems. Specialty care includes uterine fibroids, sexual health, pelvic pain, vulvar abnormalities, family planning, preconception counseling, cervical dysplasia, and anal dysplasia. A strong commitment to teaching medical students, residents and fellows, and conducting research are prerequisites for leading the Generalist Division in the role as Division Chief. Clinical investigation includes a broad range of domains, including but not limited to patient oriented, translational, epidemiologic, behavioral, outcomes, implementation or health services research. In addition, faculty will have the opportunity for daily interaction and teaching to our 28 residents and medical students. All candidates should be dedicated to providing high quality patient care and exemplary teaching. The department is composed of 30+ faculty members and is based at the University of Miami/ UHealth and Jackson Health Systems in Miami, which is easily accessible and centrally located in Miami, Florida. The Jackson Memorial Holtz Women’s & Children’s Hospital averages 4,000 deliveries a year and has a level 3 NICU staffed by UHealth neonatologists. The Women’s Hospital at Jackson Memorial has been recognized by the Maternal Safety Foundation as an Accreta Center of Excellence and as VBAC Center of Excellence. Additional responsibilities: * Outpatient clinics. * Direct care to OB/GYN patients. * Consultation for hospitalized patients on L&D service. * Consultation for nonservice unit patients by telephone. * Inpatient L&D at Jackson Holtz Women’s & Children’s Hospital * Required to cover 12 hours shifts on L&D, 6 shifts per month * Will need to use EPIC at UHealth Clinics & Cerner at Jackson Health for documentation and MobileCharge for billing. Founded in 1925 as a private non-sectarian institution and South Florida’s first university, the University of Miami is comprised of three main campuses that house 12 schools and colleges. Approximately 2,000 research studies led by over 1,650 principal investigators have resulted in over $365 million in annual research and sponsored program expenditures. The majority of this work is in biomedicine and biological sciences. Jackson Health System, opened in 1918, is the largest major teaching facility for the UMMSOM and State of Florida. It serves over 2 million citizens with its 1,550 licensed beds. The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.

Sebastian Strong Dolphins Cancer Challenge Endowed Chair, Assistant Professor, Sylvester Comprehensive Cancer Center Sylvester Comprehensive Cancer Center invites applications for a full-time, tenure-track appointment at the rank of Assistant Professor. The successful applicant will have a primary appointment in a department at the University of Miami and research responsibilities within the Translational and Clinical Oncology Program (TCO) at the Sylvester Comprehensive Cancer Center, which is South Florida’s only NCI-designated Cancer Center. The successful candidate should be motivated to participate in the expansion of driving breakthrough research from laboratory discoveries to novel interventions with direct patient impact. There is particular interest in candidates who would like to pursue greater than 50% of their time to a pediatric related cancer. We welcome highly collaborative team scientists, with a track record of excellence in research, peer-reviewed publications, and the potential to develop and/or lead clinical trials, including investigator-initiated trials. There is a particular interest in candidates interested in precision medicine/pathology. The Sylvester Comprehensive Cancer Center is a University of Miami Hospital and Clinics Facility, the only university-based cancer center in the region, and a proud member of the Alliance of Dedicated Cancer Centers. Sylvester offers the only Phase 1 clinical trials program in South Florida, providing access to some of the newest investigational therapies. Key Areas of Responsibility · Reporting to the Department Chair, the incumbent will conduct, collaborate, and manage scientific research and investigations · Participates in the management of the daily operations of his/her lab · Supervise, mentor, and manage postdoctoral fellows as well as graduate students engaged in collaborative research projects · Explore and develop appropriate research collaborations both within the Department, the Sylvester Comprehensive Cancer Center and outside of the University of Miami Miller School of Medicine departments and schools · Collect and analyze data · Write and submit scientific papers and abstracts, as well as submit grant proposals · Presents ongoing work and findings to colleagues and at academic/research conferences · Participates in the Sylvester Comprehensive Cancer Center Junior Development Program Qualifications Department Faculty members will need to meet the following requirements: Requirements (essential) · Ph.D. in Biochemistry, Chemistry or Molecular Biology and have appropriate expertise in discovery of molecular, biochemical, or chemical mechanisms. · Demonstrated knowledge and application of scientific techniques · Some experience in running a lab, funded research projects, and/or supervising post-docs · Strong written and oral communication skills · Ability to work with diverse constituency · Computer literacy · Completion of successful academic and research work that has resulted in authorship and/or co-authorship of papers in peer reviewed journals while serving as a faculty, and/or as a scientist. · Demonstrates ability to develop collaborative research projects in a manner consistent with the mentor’s research plan and contribute towards the making of scientific advances in the field of work. · Demonstrates ability to teach in the laboratory setting and/or through presentations of papers and/or seminars. · Successful track of research projects/funds and contribution to grant applications that are collaborative in nature and/or demonstrated ability to write competitive grants independently. · Demonstrates desire to move towards scientific independence through submission of grant applications, development of independent research projects, or collaborate with scientists other than the primary mentor with whom the scientist works. UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the groundbreaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research, and patient care. We're the challenge you've been looking for. The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more. The University of Miami is an Equal Opportunity Employer - Females/Minorities/Protected Veterans/Individuals with Disabilities are encouraged to apply. Applicants and employees are protected from discrimination based on certain categories protected by Federal law. Contact Information Irma Riccio 1120 NW 14th Street Miami, FL 33136 USA Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ___ to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position using the Career worklet, please review this ___. Job Status: Full time Employee Type: Faculty

Job DescriptionJob Title: HistologistJob Description We are seeking a dedicated and detail-oriented Histology Technician to join our clinical laboratory team. The ideal candidate will play a vital role in preparing tissue specimens for microscopic examination, supporting diagnostic and research activities. This position offers an opportunity to work in a dynamic healthcare environment, contributing to patient care and scientific advancement. Responsibilities • Prepare and process tissue specimens for histological analysis using various laboratory techniques., • Embed, section, and stain tissue samples following established protocols., • Ensure accurate labeling and documentation of specimens to maintain chain of custody., • Maintain strict adherence to aseptic techniques and safety standards during all procedures., • Assist with specimen collection and processing, including blood draws and other sample types as needed., • Perform quality control checks on prepared slides and troubleshoot technical issues., • Maintain detailed records of all procedures performed in compliance with laboratory regulations., • Support research projects by preparing specimens according to experimental requirements., • Collaborate with pathologists, researchers, and clinical staff to ensure accurate diagnostic results.Essential Skills, • Histology Technician/Histologist ASCP licensure in Florida required., • 2+ years' experience in hospital or research laboratories., • Proficient in laboratory procedures including specimen collection, processing, embedding, sectioning, and staining techniques., • Strong understanding of laboratory safety protocols and quality assurance practices., • Meticulous attention to detail, excellent organizational skills, and the ability to work effectively within a team.Additional Skills & Qualifications, • Familiarity with medical terminology, anatomy, physiology, and pathology concepts preferred. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Coral Gables,FL. Application Deadline This position is anticipated to close on Mar 6, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job Description The Miccosukee Tribe of Indians of Florida is looking to hire a full-time Wildlife Biologist. This is a professional position of service to the Miccosukee Tribe of Indians of Florida (“Tribe”) requiring a specialized scientific knowledge base in natural resource management, conservation, and restoration, particularly pertaining to fisheries and wildlife. The Wildlife Biologist is responsible for designing surveys, processing data, and reporting findings on native and exotic fish and wildlife for the Miccosukee Fish & Wildlife Department (FWD). Primary responsibilities include, but are not limited to: designing field surveys, data logging and processing, statistical analyses, and writing reports on studies of fish and wildlife. Secondary responsibilities include but are not limited to: assist FWD with aquaculture/fisheries operations, repair and maintenance of field equipment, nuisance wildlife capture and removal, and community outreach events. The Wildlife Biologist will communicate project logistics, data, analyses, reports, and project completion to the Projects Coordinator, but the Wildlife Biologist also maintains an open line of communication directly to the FWD Director. The Wildlife Biologist regularly works independently and in a team, with the rest of the FWD employees to ensure projects, field work, analyses, and reporting are completed such that the FWD can successfully achieve the Tribe’s research, management, conservation, and restoration goals, primarily for the ecological and cultural well-being of fish and wildlife resources across all Tribal Lands, including trust, leased, and fee title lands, and to include federal lands, such as Everglades National Park, Big Cypress National Preserve, Biscayne National Park, and USFWS National Wildlife Refuges, where the Tribe has use and occupancy rights. The FWD is organized under Sustainable Resources, which constitutes the Miccosukee Environmental Protection Agency departments (Water Resources, Land Resources, Fish & Wildlife). Sustainable Resources is led by the Chief Sustainability Officer. EDUCATION/TRAINING: A Bachelor’s of Science (B.S.) degree in Wildlife Biology, Ecology, or closely related field, is required. Must include demonstrated professional experience with wildlife in a research lab, government agency, non-governmental organization, or private company. EXPERIENCE: The incumbent must have experience in studying, capturing, and handling fish and wildlife; recreational experience may also be considered valid. The incumbent must be able to readily identify native and exotic fauna in Florida. The incumbent must have a comprehensive understanding of environmental drivers, ecology, wildlife interactions, and behavior of fish and wildlife, especially of game species and species of ecological concern. The incumbent must have experience in data logging, entry, and organization. The incumbent should have a basic understanding of mechanics, such that they can perform reasonable maintenance and repairs of equipment when in the field. Must have experience in off-road vehicle and vessel operations, maintenance, and mechanics. Must possess experience with MS Office programs (i.e., Word, PowerPoint, Excel). Must possess a valid Florida driver’s license upon hire, and must be retained throughout the duration of employment. PHYSICAL REQUIREMENTS: The incumbent must be able to work outdoors in the South Florida climate that includes extreme heat, humidity, UV exposure, and severe weather that includes heavy rain and lightning. The incumbent will expect to encounter and handle dangerous wildlife, including: large mammals/reptiles, venomous reptiles, stinging/biting insects, and noxious plants. The incumbent will be working in and around wetlands, open water ponds/lakes, and deep canals. The incumbent must be able to swim. The incumbent must be able to lift and carry up to forty (40) pounds, unassisted. Salary Negotiable Depending on Experience - Range $55,000 - $65,000 annually Drug Screen and Background Check Required. Job Site: Miccosukee Indian Reservation; 20 miles west of Krome Avenue on SW 8th Street

Mercor is recruiting Sales Representatives, Wholesale and Manufacturing, Technical and Scientific Products working on a research project **for one of the world’s top AI companies. This project involves using your professional experience to design questions related to your occupation as a Sales

About the Role** Mercor is seeking experienced Sales Representatives, Wholesale and Manufacturing, Except Technical and Scientific Products to support a leading AI lab in advancing research and infrastructure for next-generation machine learning systems.

Biology, Chemistry, Physics, Environmental Science, Earth Science, or a related field) - 2+ years of professional work experience in scientific research, laboratory work, field research, applied science, science communication, or a related domain - Active professional familiarity with scientific

Job Description La Scuola is a progressive environmental school that welcomes children from preschool – 8th grade. This is a place to learn, laugh, grow, question, work hard, develop, think big, collaborate and innovate. We emphasize collaboration and recognize the gifts that each child brings to the group. Our approach is one that recognizes the whole child and focuses first and foremost on connection and social-emotional learning and relationships as the necessary foundations for education. La Scuola is an educational home for teachers drawn to nature and practices that are rooted in unifying beliefs about children and learning, based on current neurological and educational research. La Scuola educators are both guides and co-learners in the collaborative learning process and make students’ learning visible to themselves and others. We view teaching not as a static set of skills, but as a dynamic process, manifested in our culture of research and our commitment to the children’s development. La Scuola is looking for dedicated, dynamic and experienced educators to lead classroom instruction for Grades 6 - 8. The ideal candidate will possess a strong background in education, with an ability to successfully work with the students and faculty to ensure a safe, supportive learning environment that reflects the mission and values of La Scuola. Educators interested in joining our team should also be naturally curious, life-long learners and invested in supporting our next generation of environmental stewards, problem solvers, leaders, and innovators. Our 3-acre campus inspires scientific inquiry and provides an outdoor environment that serves as an additional classroom for all of our students. If you love nature and exploring the outdoors, this is the school for you! Working at La Scuola is more than just a teaching job. It’s a chance to help build a better future – for yourself and the world. If you’re looking to make a difference and are passionate about education and the environment, we’re looking for you! We look forward to the opportunity to meet you and show you what makes our environmental school so special! Company DescriptionLa Scuola is a progressive forest school that welcomes children from ages 3 months to 8th grade. Tucked within 3 acres of lush and sprawling forest, our campus is surrounded by mature trees, an abundance of wildlife, and beautiful edible landscapes. The nature that surrounds our school is at the heart of our philosophy. At La Scuola, it is our belief that the exploration of the natural world is the richest source of learning. Our progressive school is also heavily inspired by the Reggio Emilia approach. This approach asserts that children are born capable, with innate creativity, and with a sense of wonder that should be nurtured. Our team of educators are facilitators and co-learners, working alongside our students to think deeply about the world, develop theories together, and express ideas through a multitude of “languages” as a way to share knowledge. Ultimately, La Scuola blends the principles of the Reggio Emilia approach with our love of nature to create a profound and beautiful learning journey for our students. Through rich and meaningful experiences in nature, the development of ideas and theories with facilitators and peers, and the expression of these ideas through the hundred languages of children, our students develop a lifelong love of learning, an appreciation for the environment, and a profound sense of environmental stewardship along the way.La Scuola is a progressive forest school that welcomes children from ages 3 months to 8th grade. Tucked within 3 acres of lush and sprawling forest, our campus is surrounded by mature trees, an abundance of wildlife, and beautiful edible landscapes. The nature that surrounds our school is at the heart of our philosophy. At La Scuola, it is our belief that the exploration of the natural world is the richest source of learning.\r\n\r\nOur progressive school is also heavily inspired by the Reggio Emilia approach. This approach asserts that children are born capable, with innate creativity, and with a sense of wonder that should be nurtured. Our team of educators are facilitators and co-learners, working alongside our students to think deeply about the world, develop theories together, and express ideas through a multitude of “languages” as a way to share knowledge.\r\n\r\nUltimately, La Scuola blends the principles of the Reggio Emilia approach with our love of nature to create a profound and beautiful learning journey for our students. Through rich and meaningful experiences in nature, the development of ideas and theories with facilitators and peers, and the expression of these ideas through the hundred languages of children, our students develop a lifelong love of learning, an appreciation for the environment, and a profound sense of environmental stewardship along the way.

Job Description *Authorized to work in the US Required (US Citizen Preferred) *Onsite at a SEFSC Facility (TX, FL, Gulf of Mexico, South Atlantic, or Caribbean) *Proposal Effort: Position is Subject to Contract Award *Must be able to provide 3 professional references POSITION DESCRIPTION: The Administrative Support Specialist provides essential operational and logistical support for NOAA, which collects, manages, and analyzes fishery-dependent data critical to sustainable fisheries management and protected species conservation across the Gulf of Mexico, South Atlantic, and Caribbean. This role ensures the smooth coordination of field operations, training logistics, procurement tracking, and data management activities supporting NOAA. The position requires strong organizational, communication, and technical skills to manage multiple concurrent administrative and reporting tasks in a federal scientific setting. RESPONSIBILITIES: • Provide comprehensive administrative assistance to NOAA's Observer Program leadership, trainers, and technical teams., • Coordinate logistics for observer trainings, briefings, and debriefings - including scheduling, facility setup, travel support, and materials preparation, • Manage correspondence, reports, and deliverables, including quarterly status reports, meeting minutes, and task tracking documentation., • Assist with procurement and inventory tracking, ensuring timely acquisition and documentation of sampling and safety equipment used by fishery observers., • Support financial and travel documentation, including invoice preparation, expense reconciliation, and compliance with Federal Travel Regulations (FTR)., • Process and file official program documentation, including permits, field forms, and administrative records, in accordance with NOAA and federal data retention policies., • Assist with data quality assurance, proofreading reports, reviewing spreadsheets for accuracy, and ensuring compliance with NOAA data standards., • Provide communication and coordination support between NOAA staff, contractors, and partner agencies involved in fisheries monitoring and research., • Associate's degree or equivalent experience in Business Administration, Environmental Science, Communications, or related field., • 2+ years of administrative or program support experience, preferably in a scientific, government, or environmental program setting., • Strong proficiency with Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and database systems., • Experience supporting NOAA, federal science programs, or other federal contracting environments., • Familiarity with federal acquisition and reporting procedures, including record management, FTR compliance, and SCA (Service Contract Act) labor standards., • Knowledge of marine science programs, observer operations, or fisheries management., • Experience with Adobe Acrobat, SharePoint, or government database systems for documentation management., • Excellent written and verbal communication skills with attention to detail.

Life Sciences, Health, and Wellness.January 21, 2026Position Overview.The Lab Technician conducts open lab hours to assist faculty in the day-to-day laboratory operations at a local or divisional site.Ensures that Students and faculty have adequate resources to perform all aspects of course requirem

We're currently looking for individuals across the country to take part in remote paid research, including remote focus groups, product trials, and consumer studies. Most research studies are conducted remotely at home, though some may be in-person.

Part-Time Lab Technician II (Physical Sciences).January 21, 2026Position Overview.The Lab Technician conducts open lab hours to assist faculty in the day-to-day laboratory operations at a local or divisional site.Ensures that Students and faculty have adequate resources to perform all aspects of cou

We're currently looking for individuals across the country to take part in remote paid market research, including online focus groups, product trials, and consumer studies. Most research studies are conducted remotely from home, though some may be in-person. Comfort participating in remote, market r

Part-Time Lab Technician II, Natural Science, Health and Wellness.Natural Science, Health and Wellness.October 30, 2025Position Overview.The Lab Technician conducts open lab hours to assist faculty in the day-to-day laboratory operations at a local or divisional site.Ensures that Students and facult

The Construction Project Manager will oversee a ground-up residential development from structural phase through completion.Responsibilities include budget control, schedule management, subcontractor oversight, contract administration, and regulatory compliance.This is a full-time hybrid role based i

Data Entry / Remote] - Anywhere in U.Competitive pay - As a Data Verification Analyst at Foundation AI, you will: Process, segregate, review, and validate data provided in various formats according to changing process requirements; Prepare, compile, and organize documents for data capture, ensuring

Are you a high-energy construction professional who thrives on the transition from a blueprint to a finished structure? We are seeking a.In this role, you won't just manage tasks; you'll own the lifecycle of a project.From the initial pre-construction hand-off to the final walkthrough, you will be t

Terra, the award winning, Miami-based real estate development company carefully chooses projects that have a positive impact on their surroundings and, by extension, on the people who live there.When planning a new development, Terra takes a dynamic role with the city and neighborhood to activate it

South Florida airports, seaports, roadways, and private developments.This position may be assigned to the project or head office.The position supports Project Management and Project Supervision teams for the assigned Projects.The position may also support preconstruction activities including estimat