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Job Description At K2 Medical Research, a privately-owned clinical research facility in the greater Orlando and Central Florida area, we specialize in conducting multiphasic clinical trials that promote the development of innovative and effective medical treatments while maintaining the safety and privacy of our participants. We are committed to fighting the diseases that plague our loved ones and ourselves. By harnessing the power of advanced clinical research and connecting our patients with the treatments of tomorrow, we can improve the health of our local communities, and by extent, the population of our world. We are currently seeking a bilingual (Spanish speaking) RN/Infusion Nurse and prescreener. K2 is seeking an experience RN/Infusion Nurse to support our Maitland (Orlando) clinic. This position may have flexibility for hiring as Part-time or Full-time and while it is to support for two (2) and a half months, it has the possibility of turning into long term employment. The RN/Infusion Nurse manages study patients in an outpatient-based infusion suite. They provide nursing care for patients receiving investigational therapies delivered through intravenous therapy. The Infusion Nurse follows study specific protocol guidelines and communicates and interacts with investigators, clinic staff, sponsoring agencies, and others to effectively perform required infusions and related research procedures. Primary Responsibilities: • Responsible for the insertion and maintenance of the IV line as well as the care of the patient receiving the therapy, • Establish IV access, • Administer investigation product, • Monitor patient, ensure patient safety, • Attend meetings and relay pertinent information to Infusion Team members in a timely manner, • Maintain timely source documentation as well as sponsor required information, • Complete all monitor and sponsor queries within a timely manner, • Manage all nurse functions of the Infusion suite, • Assist PI and Clinical Research Coordinator in trial related procedures such as lumber punctures, lab collections, EKG’s and more, • Assess patient’s tolerance to IP, ensuring the absence of infusion reactions, • Perform preceptor duties to provide training and guidance for employees in Infusion Nurse I roles, • Travel to affiliated sites as needed, • Potential management coverage, • Reading, understanding and adhering to organizational Standard Operating Procedures (“SOP”) and study protocols, • Working with internal staff to resolve issues, • Exploring new opportunities to add value to organization and departmental processes, • Helping others to achieve results, • Performing other duties as assigned, • Learn and support the mission and goals of K2 Medical Research, • Bilingual in English and Spanish preferred, • Valid RN license required, • Active CRNI certification preferred. If hired at a Level II without active certification, must meet this requirement within 12 months of employment start date, • At least 1 year experience in infusions or relevant role required., • Experience in a Clinical Research setting preferred Benefits • Medical, Dental, Vision, Flexible Spending Accounts, Employer paid Long-Term disability and Life Insurance, Short Term Disability, Accident and Critical Illness Insurance, Voluntary Life and Long-Term Care Insurance, Legal Shield, Employee Assistance Program, and various discount programs., • 401(K) Plans- Traditional and Roth plans are available; 4% employer match that is immediately vested, • PTO of 16 days per year, 17 days after the first year of FT employment, • 9 paid Holidays, • K2 observes a four-day work week, Monday through Thursday, for full time employees. Fridays are non-working days unless required by business needs.

Job DescriptionNow Hiring: Field Case Managers (RN or LPN) – Statewide Florida (1099) The IMA Group is actively expanding across Florida and seeking experienced Field Case Managers to join our growing 1099 network. We offer flexible, independent contractor opportunities for RNs or LPNs with at least one year of workers' compensation experience. Whether you're looking to manage a few cases or maintain a full caseload, we allow you to build a schedule that fits your availability and geographic preferences. As a Field Case Manager, you’ll oversee the medical treatment of individuals with workplace injuries, collaborating with insurance carriers, medical providers, attorneys, employers, and injured workers. Your role is critical in ensuring timely and appropriate medical care, while helping achieve return-to-work goals in a cost-effective manner. Responsibilities: • Provide comprehensive medical case management in coordination with patients, physicians, healthcare providers, employers, and referral sources., • Evaluate treatment plans for appropriateness, medical necessity, and cost-efficiency., • Coordinate Independent Medical Evaluations (IMEs) and/or perform job site evaluations., • Track patient progress, engage with providers, and offer medical recommendations to all stakeholders., • Prioritize casework effectively and develop strategic plans for care management., • Prepare timely, detailed reports and attend medical appointments as required. Qualifications:, • Current license as an RN or LPN., • Minimum of 1 year of workers’ compensation case management experience., • Malpractice Liability Insurance (or willingness to obtain)., • Strong computer/technology proficiency., • Bilingual skills preferred., • Access to a personal computer, phone, and reliable transportation for in-person appointments. The IMA Group is an Affirmative Action/Equal Opportunity Employer Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities. #LI-BC1 #LI-HYBRID

Job DescriptionNow Hiring: Field Case Managers (RN or LPN) – Orlando, FL (1099) The IMA Group is actively expanding across Florida and seeking experienced Field Case Managers to join our growing 1099 network. We offer flexible, independent contractor opportunities for RNs or LPNs with at least one year of workers' compensation experience. Whether you're looking to manage a few cases or maintain a full caseload, we allow you to build a schedule that fits your availability. As a Field Case Manager, you’ll oversee the medical treatment of individuals with workplace injuries, collaborating with insurance carriers, medical providers, attorneys, employers, and injured workers. Your role is critical in ensuring timely and appropriate medical care, while helping achieve return-to-work goals in a cost-effective manner. Responsibilities: • Provide comprehensive medical case management in coordination with patients, physicians, healthcare providers, employers, and referral sources., • Evaluate treatment plans for appropriateness, medical necessity, and cost-efficiency., • Coordinate Independent Medical Evaluations (IMEs) and/or perform job site evaluations., • Track patient progress, engage with providers, and offer medical recommendations to all stakeholders., • Prioritize casework effectively and develop strategic plans for care management., • Prepare timely, detailed reports and attend medical appointments as required. Qualifications:, • Current license as an RN or LPN., • Minimum of 1 year of workers’ compensation case management experience., • Malpractice Liability Insurance (or willingness to obtain)., • Strong computer/technology proficiency., • Bilingual skills preferred., • Access to a personal computer, phone, and reliable transportation for in-person appointments. The IMA Group is an Affirmative Action/Equal Opportunity Employer Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities. #LI-BC1 #LI-HYBRID

Job DescriptionJoin Our Team as a Hematology/Oncology Physician! Are you a fellowship-trained hematologist oncologist looking for an exciting opportunity? AdventHealth Medical Group in Lake Nona is on the hunt for a passionate physician to specialize in genitourinary cancer while managing a diverse range of hematologic and oncologic conditions. This role offers a unique blend of inpatient and outpatient care, collaboration with APRNs/PAs, and the chance to support a leading urologic oncologic surgical program. Why AdventHealth? At AdventHealth Medical Group, we pride ourselves on being part of a growing healthcare community in Orlando. We are looking for a dedicated physician to join our team by late Summer 2026. If you have a keen interest in Genitourinary Cancer and are eager to manage a variety of hematologic and oncologic conditions, we want to hear from you! Your Responsibilities: • Participate in a shared call rotation for both inpatient and outpatient care., • Collaborate with APRNs/PAs in both settings to provide comprehensive patient care., • Support one of the busiest Urologic Oncologic Surgical programs in the nation, with a surgeon who has performed over 18,000 robotic prostatectomies., • Utilize available infusion, radiation, and surgical services at Lake Nona., • Engage in multidisciplinary clinics, research, clinical trials (including Phase 1), and daily tumor boards., • Work alongside nurse navigators, social workers, chaplains, pharmacists, and nutritionists for holistic patient support., • A competitive benefits and compensation package., • Occurrence-based malpractice coverage., • Paid leave days and CME days with an allowance., • A 403b retirement plan., • Health insurance for you and your family., • Relocation allowance.Requirements:

Highlights • $33 - $38/hr based on experience, • Great benefits including 401k w/match and 15 days PTO, • Consistent schedule, no overnights or weekends, • Work with Phase I - III cardiovascular and metabolic studies! About Our Client Our client is a fast growing site network that currently has over 35 sites and constantly expanding! They focus on diversity in their trials including therapeutic areas: cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best-in-class experience for patients and sponsors. Responsibilities As a CRC you will be a specialized research professional under the direction of the clinical Principal Investigator and Site Manager. While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical trial process! • Conduct procedures such as vital signs, blood draws, EKGs, and bladder scans., • Patient recruitment, enrollment, scheduling, and consent, • Lab procedures and shipments, • Maintain GCP and follow protocols, • Data management in EDC systems, • Overall coordination of the study Qualifications: • 2+ years of experience working as a CRC on sponsor backed clinical trials, • Phlebotomy and lab processing experience (ability to perform without supervision), • Ability to work on site M-F on site (there is no remote or hybrid days)

Principal Investigator – Clinical Research 📍 Orlando, FL (relocation support available) We are searching for a Principal Investigator to join and lead studies at a high-performing clinical research site in Orlando. This role is a critical hire, ensuring continuity of operations, sponsor confidence, and patient safety across a fast-paced portfolio of cardiometabolic, pulmonary, CNS, and vaccine trials. The position is designed as a Principal Investigator role with a clear pathway to Medical Director within 6–12 months for physicians who demonstrate strong leadership capabilities. Experienced physician leaders may be considered directly for the Medical Director title. As Principal Investigator, you will: • Serve as PI on multiple active and upcoming clinical trials., • Provide medical and scientific leadership, ensuring compliance and patient safety., • Oversee study conduct and data integrity while building trust with sponsors and CROs., • Collaborate with sub-investigators and clinical staff, with potential to step into a broader leadership role., • Adapt to a high-volume site environment with flexibility for occasional evenings/weekends. The Ideal Profile • MD/DO, • Minimum 3+ years of clinical research experience with PI responsibility on at least 5 studies (industry or relevant academic)., • Licensed to practice in the U.S.; board certification a plus., • Energetic, diplomatic, and able to thrive in a collaborative, diverse team., • Spanish-speaking strongly preferred (but not required)., • Experience across cardiometabolic or pulmonary trials highly valued; additional exposure to vaccines or CNS desirable., • Leadership or site management experience a plus, or demonstrated potential to step up quickly. Compensation & Benefits • Principal Investigator: ~$275,000 base + ~20% bonus (OTE $300–315K)., • Medical Director: $250,000–$350,000 OTE (higher for exceptional profiles)., • Relocation/sign-on bonus available. Why This Role? This opportunity is ideal for a physician who wants to: • Step into a pivotal role at a high-demand, growth-focused research site., • Build on PI experience with the potential to progress into Medical Director., • Work across a diverse therapeutic portfolio with a heavy focus on cardiometabolic and pulmonary studies., • Join a respected clinical research network backed by strong national growth. Next Steps Interviews are being scheduled on a rolling basis with an urgent target start date. If you meet the requirements and are open to a confidential conversation, please apply for a discreet discussion.

The Orlando Health Cancer Institute is seeking a Board Certified/Board Eligible Gynecologic Oncologist to join our multidisciplinary Gynecologic Oncology team at The Center for Women s Health at Orlando Health Lake Mary Hospital. Responsibilities include diagnosis and treatment of cancers of the ovaries, vagina, uterus, cervix, vulva as well as complex gynecologic issues. Additional responsibilities include genetic coordination, management of chemotherapy and coordinating multidisciplinary care with Radiology, Radiation Oncologists and Pathologists. Both Surgery and chemotherapy experience are requirements of this role. You will be joining another practitioner at this location. Location: Lake Mary Hospital Lake Mary, Florida Role Requirements: • Board Certified/Board Eligible Gynecologic Oncology., • Thriving physician-led, professionally managed healthcare system., • Collegial and supportive division environment with a variety of experience levels., • State of the art Operating rooms and equipment., • Participation in Phase 1-3 clinical trials., • Access to monthly multidisciplinary gyn onc tumor board meetings., • Excellent brand recognition, with new patients seeking out Orlando Health Cancer Institute for their care., • Integrated multidisciplinary and subspecialized practice environment., • Great payor mix with patients from top Orlando employers and Orlando Health team members., • Robust operational support and resources in a collaborative work environment., • Dynamic administration that fosters physician autonomy when it comes to clinical decision making and patient outcomes., • Opportunity for professional growth and leadership development., • Excellent compensation package, opportunity to make more based-on productivity., • Benefits package includes time away for vacations and conferences, health/vision/dental insurance along with full malpractice coverage, disability coverage, deferred compensation and retirement savings options., • Generous sign-on bonus with eligibility for an annual bonus. Community Information: • There is no state income tax., • Greater Orlando offers direct access to Florida s world-famous theme parks and attractions., • Our lifestyle options have something for everyone, from the downtown districts for those enjoying a trendy urban flair, to family-oriented communities with top rated public and private schools. Orlando Health Lake Mary Hospital is a comprehensive acute care facility representing the next phase of growth for Orlando Health and its Lake Mary campus. At 320,000 square feet, the hospital s five- and six-story towers will have a 240-bed capacity. The facility will include six state-of-the-art operating rooms, three catheterization labs with a dedicated interventional radiology and vascular lab offering comprehensive cardiovascular care, a 16-bed intensive care unit, medical-surgical bed units, an observation unit and an on-site outpatient pharmacy. A key focus area for the new hospital will be women s health, including labor and delivery services, and a future neonatal intensive care unit. At the Center for Women s Health at Orlando Health Lake Mary Hospital, we focus exclusively on the needs of woman. Our scope of care includes in-patient care obstetrics and gynecology services, specialty care including minimally invasive surgery, breast and gynecological cancer care, you can count on our multidisciplinary team to offer expert and compassionate care, close to home. Bringing together multiple healthcare services at one convenient location, the hospital will be connected to the existing Orlando Health Emergency Room Lake Mary, which opened in September 2019 and features 25 treatment rooms with full imaging and lab services. Patients have access to full-service emergency care with advanced medical technology provided by top physicians and staff. Next door on the campus is the 60,000-square-foot Orlando Health Medical Pavilion offering several outpatient specialties, including pulmonology, pediatrics, obstetrics and gynecology, urology, orthopedics, general surgery, cardiology and cardiac rehab. Coordinated services from Orlando Health s network of providers all in one location gives patients access to both comprehensive and convenient care. Orlando Health Cancer Institute One of the largest cancer care providers in Florida, Orlando Health Cancer Institute is guided by its vision to be a national leader by providing exceptional cancer care and a personalized experience. The realization of that vision includes a focus on an expanding footprint, enhanced services and treatments, advancements in technology, and an ever-growing team of interdisciplinary cancer experts specializing in more than 200 types of cancer. The institute s dedicated medical staff consists of more than 60 medical, surgical and radiation oncologists, as well as pathologists, advanced practice providers, nurse and clinical specialists, and support staff such as pharmacists, dietitians and counselors. We also reach across specialties as needed, into areas like neurosurgery, pancreatology, colon and rectal surgery, and endocrinology. This multidisciplinary team approach means that each patient benefits from the expertise of a team of specialists who work together to develop a coordinated, personalized care plan, across the cancer-care continuum. These teams meet several times a week in tumor boards to talk through each patient s treatment plan and progression. The institute continues to introduce and further novel technologies to ensure top-notch services, such as new advanced radiation and proton therapies, bone marrow transplant and cellular therapy, and cancer-related aesthetic and reconstructive procedures. Through a robust research program, the institute also supports physician involvement in numerous research studies and clinical trials that gives patients access to innovative diagnosis, treatment and symptom management options. While the institute s comprehensive care includes an expert team of medical professionals, advanced technology and leading-edge research, we recognize there is more to cancer care. To treat the whole person body, mind and spirit the institute offers supportive and palliative care, cancer genetic counseling and high-risk care, and complementary services through various wellness programs, integrative medicine and a Cancer Support Community. In addition to an all-inclusive facility on Orlando Health s downtown campus, Orlando Health Cancer Institute has five additional treatment locations, in Clermont, Dr. Phillips area, St. Cloud, Lake Mary and Ocoee; more than 10 practice locations; and expanded options for virtual appointments and consultations. By continuing to extend the institute s reach and expand its services, area residents are assured comfortable, convenient access to world-class cancer services in the familiarity of their own communities. Orlando Health Cancer Institute provides award-winning, nationally recognized and accredited cancer services in Central Florida. Some of our recognitions and distinctions include: • 60 Hospitals and Health Systems with Great Oncology Programs Becker's 2023, • Best Hospitals for Cancer (top 100) U.S. News & World Report, 2023-24, • American College of Surgeons (ACoS) Commission on Cancer (CoC), • National Accreditation Program for Breast Care Centers (NAPBC), • Radiation Oncology Department accreditation American College of Radiology (ACR), • Medical Oncology Clinics certification Quality Oncology Practice Initiative (QOPI ) Certification Program, an affiliate of the American Society of Clinical Oncology (ASCO), • National Accreditation Program for Rectal Cancer (NAPRC), • Bone Marrow Transplant and Cellular Therapy Program accreditation Foundation for the Accreditation of Cellular Therapy (FACT)

Orlando Health Cancer Institute seeks on-site, full-time, ABR fellowship trained Breast Imagers to join our expanding practice of breast radiologists within the Orlando Health Cancer Institute. Workdays consist of breast imaging and breast biopsies with an opportunity to participate in clinical research. Our Breast Imagers are integral for the multidisciplinary cancer teams and participate in weekly tumor boards. Orlando Health Cancer Institute comprises 8 sites of care across central Florida, including full radiology capabilities. All sites of care are developing complete breast services including imaging, surgery, chemotherapy and radiation. Orlando Health Cancer Institute has over 1000 employees, with over 100 physicians and APP s all dedicated to specialized cancer care. Potential locations include: • Orlando Health Winnie Palmer Outpatient Women's Imaging at 105 W. Miller, Orlando, FL., • Orlando Health Imaging Center - Oviedo - 1675 W. Broadway St., Oviedo, FL., • Orlando Health South Lake Hospital - 1900 Don Wickham Dr., Clermont, FL., • Orlando Health - Health Central Hospital - 10000 W. Colonial Dr., Ocoee, FL., • Orlando Health Dr. P. Phillips Hospital - 9400 Turkey Lake Rd. Orlando, FL.Candidates can expect:, • Extremely competitive base compensation, bonus opportunities, • Full-time, part-time or Float positions available, • Working within an all-inclusive, high-volume group, • Utilizing the Epic comprehensive health record keeping system, • Stereotactic, MRI, ultrasound procedures, and iodine seed localizations, • Implemented tomosynthesis (3-D imaging), • Phillips PACS and PowerScribe systemsPractice Highlights:, • Thriving physician-led, professionally managed healthcare system., • Excellent brand recognition., • Great payor mix with patients from top Orlando employers and Orlando Health team members., • Robust operational support and resources in a collaborative work environment., • Dynamic administration that fosters physician autonomy when it comes to clinical decision making and patient outcomes., • Opportunity for growth and leadership development., • Opportunity to expand an active research and innovation program.Financial Package:, • Excellent compensation package, opportunity to make more based-on productivity., • Benefits package includes time away for vacations and conferences, health/vision/dental insurance along with full malpractice coverage, disability coverage, deferred compensation and retirement savings options., • Generous sign-on bonus with eligibility for an annual bonus., • 4 weeks of continuous pay for parental leave., • CME Stipend, • Eligible employer under the Public Student Loan Forgiveness ProgramCommunity Information:, • There is no state income tax., • Offers direct access to Florida s world-famous theme parks, attractions and beaches., • Our lifestyle options have something for everyone, from the downtown districts for those enjoying a trendy urban flair, to family-oriented communities with top rated public and private schools. The institute continues to introduce and further novel technologies to ensure top-notch services, such as new advanced radiation and proton therapies, bone marrow transplant and cellular therapy, and cancer-related aesthetic and reconstructive procedures. Through a robust research program, the institute also supports physician involvement in numerous research studies and clinical trials that gives patients access to innovative diagnosis, treatment and symptom management options. While the institute s comprehensive care includes an expert team of medical professionals, advanced technology and leading-edge research, we recognize there is more to cancer care. To treat the whole person body, mind and spirit the institute offers supportive and palliative care, cancer genetic counseling and high-risk care, and complementary services through various wellness programs, integrative medicine and a Cancer Support Community. In addition to an all-inclusive facility on Orlando Health s downtown campus, Orlando Health Cancer Institute has five additional treatment locations, in Clermont, Dr. Phillips area, St. Cloud, Lake Mary and Ocoee; more than 10 practice locations; and expanded options for virtual appointments and consultations. By continuing to extend the institute s reach and expand its services, area residents are assured comfortable, convenient access to world-class cancer services in the familiarity of their own communities. Orlando Health Cancer Institute provides award-winning, nationally recognized and accredited cancer services in Central Florida. Some of our recognitions and distinctions include: • 60 Hospitals and Health Systems with Great Oncology Programs Becker's , 2023, • Best Hospitals for Cancer (top 100) U.S. News & World Report, 2023-24, • American College of Surgeons (ACoS) Commission on Cancer (CoC), • National Accreditation Program for Breast Care Centers (NAPBC), • Radiation Oncology Department accreditation American College of Radiology (ACR), • Medical Oncology Clinics certification Quality Oncology Practice Initiative (QOPI ) Certification Program, an affiliate of the American Society of Clinical Oncology (ASCO), • National Accreditation Program for Rectal Cancer (NAPRC), • Bone Marrow Transplant and Cellular Therapy Program accreditation Foundation for the Accreditation of Cellular Therapy (FACT)

Job Description Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. We are actively hiring a Regulatory Specialist at the Flourish Research site in Winter Park, FL! The Regulatory Specialist is responsible for managing and coordinating regulatory documents and activities for clinical research studies conducted at Flourish Research. This role involves working with site leadership, principal investigators, and regulatory bodies to ensure compliance with Flourish Research's standards, federal regulations, and sponsor protocols. Shift: Monday - Friday, 8 AM - 5 PM Location: 1788 W Fairbanks Ave, Suite A, Winter Park, FL 32789 Compensation: Competitive hourly rate based on experience Benefits: Health, dental, and vision insurance plans, 401(k) with 4% match, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 10 company holidays. RESPONSIBILITIES • Prepare, maintain, and oversee all research-related regulatory documents, • Manage the full lifecycle of regulatory submissions to IRBs, sponsors, and regulatory agencies, • Submit study updates, including amendments, safety info, FDA 1572s, and consent forms, • Maintain accurate logs and ensure proper regulatory filing and archival of documents, • Prepare for monitoring visits and audits, • Distribute, collect, and track essential site regulatory documents (CVs, licenses, training certs, etc.), • Maintain both paper and electronic regulatory files for all active studies, • Ensure confidentiality of study protocols and Protected Health Information (PHI), • Draft clear, error-free written communications and documentation, • Execute duties safely, efficiently, and in alignment with company policies, • Represent Flourish Research professionally in all internal and external interactions, • High school diploma or equivalent required; college degree preferred, • 0–3+ years of experience in clinical or biological research, • Proficient in Microsoft Office (Outlook, Word, Excel) and platforms such as CTMS, eRegs/eDocs, • Highly detail-oriented, organized, and self-motivated, • Able to work independently and collaboratively in a fast-paced environment, • Strong written and verbal communication skills, • Ethical and professional in interactions with patients, sponsors, IRBs, and staff, • Strong critical thinking and problem-solving abilities, • Demonstrates a high level of professionalism and work ethic, • Flexible and willing to take on additional tasks as needed, • Effective at cross-departmental collaboration and issue resolution, • Contributes to departmental initiatives and process improvements, • Assists in training new team members, • Meets or exceeds 80% of annual goals Flourish Research is where clinical trials thrive. Flourish Research represents one of the industry's most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of cardiology/metabolic disorders/renal, CNS, pulmonology, and vaccines. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. Flourish Research strives to build an organization that attracts and leverages diversity in our staff, which reflects the diversity of our local communities. We promote education, acceptance, and inclusion because there is beauty in diversity. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU! It is the policy of Flourish Research not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, or veteran status. Powered by JazzHR kkwLdYthc2

Job Description Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. We are actively hiring a full-time and part-time Principal Investigator at our Winter Park, FL location! The Principal Investigator (PI) provides overall medical leadership and accountability for clinical research studies conducted at the site. This role ensures participant safety, scientific integrity, and strict adherence to GCP, IRB, and sponsor protocols. The PI oversees study conduct end-to-end—from feasibility through closeout—while mentoring Sub-Investigators and site staff and delivering an impeccable patient experience in every, single interaction. Shift: Monday–Friday, 8 AM – 4:30 PM (occasional weekends) Location: 1788 W Fairbanks Ave Suite A, Winter Park, FL 32789 Compensation: Competitive base salary Benefits: Health, dental, and vision insurance plans, 401k with 4% match, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 10 company holidays. RESPONSIBILITIES • Provide medical oversight for all assigned studies, ensuring compliance with protocol, GCP/ICH, IRB requirements, and applicable regulations, • Protect participant safety by assessing eligibility, conducting or overseeing exams, reviewing labs and ECGs, and making risk–benefit determinations, • Lead the informed consent process and ensure proper documentation and patient comprehension; personally consent participants as appropriate or supervise designees, • Evaluate, document, and attribute AEs/SAEs; ensure timely medical review and reporting to Sponsor/CRO/IRB per requirements, • Participate in site qualification, initiation, monitoring, and closeout visits; serve as primary medical liaison with Sponsors, CROs, and auditors, • Review and approve source data, EDC entries, medical narratives, and query responses; ensure data integrity and ALCOA+ standards, • Oversee delegation of duties to Sub-Investigators and site staff; maintain and sign the DOA log and FDA Form 1572 (or equivalent) as required, • Ensure proper management of IP per protocol and regulations; verify accountability via oversight of site procedures, • Support patient recruitment, retention, and enrollment strategies while upholding ethical standards and subject privacy, • Lead and mentor cross-functional site teams; provide ongoing training on protocol-specific procedures and GCP, • Maintain complete and current regulatory documentation, medical licensure, CV, and mandatory training (e.g., GCP, IATA, CPR) as required, • Drive continuous improvement, CAPA implementation, and inspection readiness across studies and site operations, • Represent Flourish Research professionally in all internal and external interactions, • MD or DO degree required; active, unrestricted Florida medical license in good standing, • Board certification/eligibility in a relevant specialty (e.g., Internal Medicine, Family Medicine, Cardiology, Neurology, Pulmonology) preferred, • 2–5+ years of clinical research experience as a PI or Sub-Investigator strongly preferred; prior independent PI experience preferred, • Thorough knowledge of ICH-GCP, FDA regulations, and IRB processes, • Proven ability to assess medical eligibility, manage safety events, and ensure protocol adherence, • Strong leadership with effective collaboration across research teams and stakeholders, • Excellent written and verbal communication; ability to explain complex information to participants clearly and compassionately, • Proficiency in Microsoft Office 365 and comfort with EDC/eSource and CTMS platforms, • High ethical standards and professionalism with meticulous attention to detail and data quality, • Adaptable, solution-oriented, and committed to meeting or exceeding performance goals Flourish Research is where clinical trials thrive. Flourish Research represents one of the industry's most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of cardiology/metabolic disorders/renal, CNS, pulmonology, and vaccines. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. Flourish Research strives to build an organization that attracts and leverages diversity in our staff, which reflects the diversity of our local communities. We promote education, acceptance, and inclusion because there is beauty in diversity. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU! It is the policy of Flourish Research not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, or veteran status. Powered by JazzHR PyIsQv04sk

Clinical Research Coordinator I (CRC I) Location: Orlando, FL (onsite, Monday–Friday, 8:00 AM – 5:00 PM) Role Summary: Join our growing team as a Clinical Research Coordinator I, contributing to the execution of high-volume clinical trials in nephrology. This role focuses on patient visits, lab work, data management, and supporting site operations, with opportunities for professional growth in a fast-paced environment. Key Responsibilities: • Conduct patient visits, including scheduling, blood draws, and lab processing (2–3 patients/day; 4–5 hour visits)., • Manage patient eligibility, informed consent, and record-keeping., • Perform data entry, query resolution, and CTMS updates., • Communicate with monitors and assist during weekly monitoring visits., • Ensure protocol and regulatory compliance, including IRB reporting and adverse event documentation., • 3–5 years of CRC experience with high-volume trials (15–20 active, 5–6 pending startup)., • Proficient in blood draws and lab procedures., • Knowledge of CTMS platforms., • GCP certification., • Bilingual (English/Spanish) a plus., • Empathy and excellent bedside manner., • Ability to handle challenging patient interactions professionally., • Fast-growing SMO with multiple growth opportunities., • Collaborative, team-oriented environment., • Focused onsite role—no travel required.

Job Description ***This is a 100% on-site role located at our office in Maitland, Florida. We are empowering the fight against incurable diseases. SiteRx strives to give patients hope. Today, the "best" option for a patient diagnosed with an incurable disease is a prescription that, at most, temporarily improves symptoms. In the face of this stark prognosis, an alternative option provides an avenue for hope: clinical trials. Your Mission: The Patient Liaison will be responsible for all patient engagement and care coordination activities related to treatment communications directed by patients' healthcare providers, including facilitating patients' education and understanding about available clinical research opportunities. About the Engagement: • Handle 50+ outbound and inbound calls a day with patients and caregivers to conduct education and engagement, and respond to interest in participating in clinical trials., • Ensure accurate collection and entry of patient information into the relevant databases while on the phone, • Ensure individualized, caring, courteous, and efficient service, • Support other members of your team as well as cross-functional team members, • Bachelor's degree, Associate's degree or equivalent, • Minimum 2+ years of Call Center/Contact Center management experience, • Documentation in a customer service environment, medical documentation is preferred, • Medical terminology a plus, • Bilingual (Spanish/English) a plus, • Prior inside sales experience a plus, • Possess exceptional organizational skills and attention to details, • Critical-thinking skills, • Display excellent verbal and written communication skills, • Ability to self-manage time and balance multiple priorities, • Able to quickly adapt to changes in responsibilities, workloads, and priorities, • Be a fast learner with the capacity to retain and differentiate key enrollment criteria across clinical trials, • Demonstrate a focus on process improvement and be capable of articulating ideas for improving efficiency and maximizing results, • Prior history delivering excellent customer service is required; call center experience a plus, • Possess well-developed interpersonal skills and an ability to work well independently, as well as with co-workers, peers, supervisor, and external customers, • Able to maintain confidentiality with HIPAA guidelines, patient information, and other sensitive information, • Demonstrate professionalism, sense of urgency, and self-motivation to achieve required metrics SiteRx is a fast-paced and motivated company that operates with the urgency and pace needed to democratize access to clinical research with a mission of contributing to efforts to cure currently incurable diseases. SiteRx strives to engage individuals who challenge themselves and the status quo, constantly reimagining processes and driving efficiencies both within the business and with our relevant industry partners. Benefits: • Health insurance, • Dental insurance, • Vision insurance, • Life insurance, • Paid time off, • 401(k)

Join our growing team as a Clinical Research Coordinator I, contributing to the execution of high-volume clinical trials in nephrology. Clinical Research Coordinator I (CRC I). This role focuses on patient visits, lab work, data management, and supporting site operations, with opportunities for prof

While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical

Excellent communication and stakeholder management skills.

Top 3 SkillsEnterprise Project Management & SDLC Expertise: 7+ years of project management experience managing large-scale, complex enterprise projects within the Software Development Lifecycle (SDLC). Risk & Dependency Management: Demonstrated ability to manage complex, interdependent timelines and

As Assistant Project Manager, you will be responsible for the project costing, safety, scheduling, budget and overall management of the day to day operations of the site.

Tool Stack Proficiency: Strong practical familiarity with JIRA for complex project management, Splunk for monitoring, and ServiceNow for change management and ticketing. DevOps Tooling & Operational Efficiency: Implement and manage project tracking and operational efficiency utilizing JIRA at scale

The role blends program/project management, team leadership, delivery execution, and strong business and financial acumen. Direct management of single project budgets $5M–$10M and program budgets $11M+.

Contribute to hiring, onboarding, and continuous development of project management talent.

Bachelor's degree in Civil Engineering, Mechanical Engineering, Construction Management, or other relevant degree.

This role gives you the opportunity to manage complex hospital facilities with precision, ensuring projects are delivered safely, efficiently, and to the highest standards.Direct hospital construction projects, coordinating all aspects of planning, execution, and closeout.Manage project budgets, sch

Extensive experience (10+ years) in project management or technical leadership on water/wastewater/conveyance projects.

The ideal candidate is detail-oriented, driven, and eager to grow their expertise in both project management and construction estimating. Bachelors degree in Construction Management, Civil Engineering, Architecture, or related field preferred. Minimum of 5 years of experience in construction project

Report on departmental performance and strategic initiatives to senior management. Report on team performance and operational issues to upper management. Project Management experience in electrical services and construction.

Site Management & Oversight: Oversee day-to-day field operations, ensuring work is executed to the highest quality standards and in compliance with all safety regulations and building codes. Proficiency with construction management software such as Procore and Microsoft Office tools. High school dip

Report on team performance and operational issues to upper management. Project Management experience in electrical services and construction. Electrical field experience coordinating with construction management.

This company is truly one of the most reputable and best builders in all of Florida.They are based in South Florida, have been in business for over 50 years, are completely client focused, do almost 100% negotiated work, and are growing due to their excellent reputation.They have started a new multi

Strong business acumen in project planning and management.

Minimum 2 years of experience in corporate project management.

ITS Project Manager (Full-Time, On-Site).ITS (Intelligent Transportation Systems) Project Manager.This position serves as the primary point of contact and is responsible for the overall coordination, quality assurance, and successful delivery of all contract requirements.The Project Manager ensures

There is great opportunity to work on unique projects with a local focus to make a difference, while performing site development engineering and project management tasks for residential and commercial projects. Ability to manage multiple projects and deliverables simultaneously, great time managemen

Procurement & Material Management. Minimum of 5 years of commercial HVAC or mechanical construction project management experience. Proficiency in project management tools (e.

Support business development efforts and client relationship management. Ambition and aptitude for future leadership and office management responsibilities.

Procurement & Material Management. Minimum of 5 years of commercial HVAC or mechanical construction project management experience. Proficiency in project management tools (e.

Hays has recently met with one of the highest rated General Contractors in the entire country.With 135 years in the construction industry, this company has become one of the most trusted builders of healthcare facilities in California.Most of their work is for big clients such as Kaiser Permanente,

Procurement & Material Management. Minimum of 5 years of commercial HVAC or mechanical construction project management experience. Proficiency in project management tools (e.

Ability to manage multiple projects and deliverables simultaneously, great time management skills. Experience with detailed site layout and grading; drainage and stormwater management design; utility design; and erosion and sediment control design. There is great opportunity to work on unique projec

IT project management, with at least 3+ years managing.

Ability to manage multiple projects and deliverables simultaneously, great time management skills. Experience with detailed site layout and grading; drainage and stormwater management design; utility design; and erosion and sediment control design. There is great opportunity to work on unique projec

Bachelor's degree in Construction Management, Civil Engineering, Architecture, or related field preferred. Minimum of 5 years of experience in construction project management, drywall experience strongly preferred. The ideal candidate is detail-oriented, driven, and eager to grow their expertise in

Lead storm water management design, hydrologic/hydraulic analysis and design and SWPPP preparation;. Strong client development and client management abilities;.

We are looking for someone who:.Wants to leave behind the typical structured, 8-5 desk job.Is willing to bet on themselves and be financially rewarded for it.Enjoys problem solving within a fast-paced environment.Wants an autonomous position with support as needed.Has grit, resilience, and loves a c

Minimum 2 years of experience in corporate project management.

We are looking for someone who:.Wants to leave behind the typical structured, 8-5 desk job.Is willing to bet on themselves and be financially rewarded for it.Enjoys problem solving within a fast-paced environment.Wants an autonomous position with support as needed.Has grit, resilience, and loves a c

Client of ours with a strong upcoming pipeline of healthcare projects, are looking to add an experienced project manager for their local projects.This company have a strong reputation in the industry and want to provide the right candidate with key responsibilities on high value builds.Direct experi

We are looking for someone who:.Wants to leave behind the typical structured, 8-5 desk job.Is willing to bet on themselves and be financially rewarded for it.Enjoys problem solving within a fast-paced environment.Wants an autonomous position with support as needed.Has grit, resilience, and loves a c

Strong client development and client management abilities;. Lead storm water management design, hydrologic/hydraulic analysis and design and SWPPP preparation;.