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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 Description COMPANY DESCRIPTION Charter Research is a highly experienced and quickly growing clinical research company, based in Florida and Illinois, that is looking to add to our team to help us fulfill our mission of discovering future medicines. Our company is locally owned and prides itself on providing exceptional patient experience to our participants, as well as offering agile recruitment strategies to our sponsors. Above all, we are a team, and we are seeking the right team member to add to our foundation in Orlando, FL. POSITION OVERVIEW The Event Coordinator is responsible for planning, executing, and speaking at a wide variety of marketing events with the goals of: 1.) generating a high volume of qualified leads for the site’s Recruitment Team, and 2.) cultivating a positive community image for Charter Research. The Event Coordinator has further responsibility for growing the company’s events in number, frequency, and size. RESPONSIBILITIES • Study the clinical trial protocols to determine the target audience of each study and design marketing events to reach these potential study participants., • Plan, execute, and speak at a wide variety of educational and/or entertaining community events., • Ensure all events are appropriately staffed and smoothly operated and that Charter Research is always represented professionally., • Coordinate closely with Marketing and Recruitment Team Members regarding event scheduling, staffing, and logistics to ensure success of events., • Track results of all events – including but not limited to RSVPs (#), actual attendance (#), no-show rate (%), information cards collected (#), information card collection rate (%), prescreens scheduled (#), percent of leads scheduled for prescreen (%), total event cost ($), and cost per scheduled prescreen ($)., • Report event results to Marketing Team Lead and CEO, and adjust tactics as necessary to optimize results., • Thoroughly understand the business of Charter Research, the currently enrolling studies, and study participants’ frequently asked questions, and be willing and prepared to speak knowledgably before individuals, small groups, and large audiences., • Develop and implement plans to grow the number of events, frequency of events, and attendance at events., • Support the Recruitment Team in making recruitment calls as part of follow-up after large events., • Support a wide variety of other marketing and recruitment projects and tasks, as requested by the Marketing Team Lead and/or Recruitment Team Lead, and perform additional duties as assigned., • Other duties as assigned. KNOWLEDGE, SKILLS, AND ABILITIES • Strong sense of self-confidence, with excellent public speaking and presentation skills., • Strong ability to communicate clearly and effectively, both verbally and in writing., • Ability to work independently and as a part of a team., • Demonstrated ability to work in a fast-paced environment., • Excellent organizational skills, ability to prioritize, and multi-task., • Proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook). QUALIFICATIONS Language • Prolonged periods of sitting at a desk and working on a computer., • Prolonged periods of standing, bending, and reaching.

Job DescriptionDescription: Simulation Center Coordinator South College - We are one of the nation’s fastest growing institutions of higher learning … come grow your career with us. In order to fully meet our Mission to our students, we require a diverse combination of perspectives, backgrounds, life experiences, and ideas from our faculty and staff and will provide them with an equitable and inclusive work environment -where respect and open interchange of ideas are at the heart of that culture. Over 16,000 Students 10 Campuses Competency Based Education Online Simulation Center Coordinator Description South College Orlando is seeking a skilled Simulation Center Coordinator to join our team! Our Simulation Coordinator will work in the following ways: General Responsibilities • Participates in the development, implementation and evaluation of the simulation curriculum that conforms with South College’s mission, goals, and objectives, • Research vendors for supplies and equipment, obtain bids, and make purchasing decisions within delegated authority., • Conduct tours of the facilities., • Promote revenue stream training services to local external healthcare and emergency response organizations., • Supervise preventive maintenance of equipment according to manufacturers' recommendations. Monitor scheduled maintenance to ensure that equipment is operational. Work with manufacturers or vendors to correct equipment deficiencies in order to minimize down time., • Provide BLS, ACLS, and PALS training to health science students and faculty, • Evaluate, revise, coordinate and deploy simulation curriculum, • Instruct didactic year students, participating as Course Director as directed, • Assist in the preparation for didactic lab activities throughout the didactic and clinical quarters, • Participate in the Didactic Curriculum Committee to evaluate and develop curriculum, • Participate in committees at the department and college levels, • Monitor equipment and supply levels, replacing items as needed in concert with the Department leads and pursuant to budget approval, • Assist in other departments as needed, • Strong organizational skills and keen attention to detail, • Adept interpersonal and communication skills, • Skillful problem-solving capabilities, • An ability to work effectively in a team environment with faculty, staff and administration, • Excellent written and oral communication skills, • Computer skills in MS Word, Excel, and PowerPoint Minimum Education • At least three years of clinical experience, • Experience in high-fidelity simulation in an academic environment, • AHA instructor (or eligible) Preferred Experience • Nursing or other direct patient care background

Job Description Clinical Research Nurse Coordinator II MUST HAVE CLINICAL RESEARCH experience Permanent role with full benefits on day 1 Shift: M-F 6:45 am - 3:15 pm Key Responsibilities: • Plan, coordinate, and perform nursing care for research participants, • Execute study protocols and maintain accurate documentation, • Perform physical assessments, phlebotomy, and IV insertions, • Maintain a clean and prepared clinical space, • Review informed consent documents and ensure ongoing patient advocacy, • Manage study records, medications, and test articles securely, • Communicate effectively with investigators, sponsors, and healthcare teams, • Coordinate support staff and ensure adherence to research protocols, • Registered Nurse (RN) with active licensure, • MUST HAVE CLINICAL RESEARCH experience, • Knowledge of FDA regulations, ICH/GCP guidelines, and HIPAA, • Strong interpersonal, organizational, and documentation skills, • Ability to work independently and manage multiple protocols The pay range for this position is $83200.00 - $98000.00/yr. Benefits from Day One Paid Days Off from Day One Student Loan Repayment Program Career Development Whole Person Wellbeing Resources Mental Health Resources and Support Pet Insurance* Workplace Type This is a fully onsite position in Orlando,FL. Application Deadline This position is anticipated to close on Oct 21, 2025. 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 Job Title: Health Services Coordinator (Regulatory) Location: Orlando, FL ONSITE Position Summary: We are seeking a detail-oriented and motivated Regulatory Coordinator to join our growing team. This position is ideal for graduates with a degree in Healthcare Administration, Public Health, or a related field who are passionate about clinical research and regulatory compliance. Key Responsibilities: • Assist in the preparation, submission, and tracking of regulatory documents for clinical trials., • Maintain accurate and organized regulatory files in accordance with company SOPs and applicable regulations., • Communicate with internal teams, sponsors, and regulatory agencies to ensure timely approvals and updates., • Support the development and maintenance of study-specific regulatory binders and documentation., • Bachelor’s degree in Healthcare Administration, Public Health, Life Sciences, or a related field., • Strong organizational skills and attention to detail., • Excellent written and verbal communication skills., • Ability to manage multiple tasks and deadlines in a fast-paced environment., • Proficiency in Microsoft Office Suite (Word, Excel, Outlook)., • Opportunity to launch your career in clinical research and regulatory affairs., • Supportive team environment with mentorship and training., • Competitive salary and benefits package. The pay range for this position is $23.00 - $23.00/hr. 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 ORLANDO,FL. Application Deadline This position is anticipated to close on Oct 27, 2025. 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.

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)

The Division of Pediatric Gastroenterology and Nutrition seeks a ninth pediatric gastroenterologist to join a growing academic and clinical division! The position provides an exciting opportunity to pursue an active academic career in pediatric gastroenterology and nutrition. Physicians with Advanced Endoscopy experience (i.e., ERCP with sphincterotomy and stent placements, Endoscopic Ultrasound with Fine needle aspiration, double balloon enteroscopy, endoscopic submucosal dissection, POEM, G-POEM, Endoknife, Transnasal Endoscopy) are encouraged to apply. Physicians with a passion for undergraduate and graduate medical education and wanting to partner in the establishment of a pediatric gastroenterology fellowship program are also encouraged to apply. Current faculty is comprised of 8 pediatric gastroenterologists, two of which are primarily affiliated with a partner hospital. Four full time nurse practitioners, 2 registered dietitians, 1 research coordinator, 2 social workers/licensed clinical therapists, 2 clinical coordinators and 1 family support and advocacy coordinator play integral roles in our vibrant and busy division. We are supported by the presence of all major pediatric subspecialists. We have an integrated and coordinated GI/Surgery program alignment, with specific focuses on Motility, Polyposis, Short Gut/Intestinal Rehabilitation and Inflammatory Bowel Disease. Imbedded in the GI Division are Centers dedicated to Feeding Disorders, Celiac Disease, Inflammatory Bowel Disease, Intestinal Rehabilitation and complex Motility disorders. In addition, the Division has a long standing clinical and research interest in Disorders of Brain-Gut Interactions, Celiac disease, and Eosinophilic Gastrointestinal Diseases. Our division plays an integral part in the multidisciplinary care of patients with cystic fibrosis and Aerodigestive disorders. Responsibilities of these positions include providing direct patient care in inpatient and ambulatory settings, medical education of students and trainees, and participation in clinical research and/or quality improvement. The start date is negotiable, and the position will remain open until filled. The successful candidate will have experience and knowledge of all pediatric GI and hepatology disorders; demonstrated skills in the full gamut of pediatric GI endoscopic and other procedures; and excellent communication and team skills. The candidate will have completed fellowship in good standing in Pediatric Gastroenterology at RRC-approved fellowship program (or equivalent), MD (or equivalent) degree, Board Certified in Pediatrics, and BE/BC in Pediatric Gastroenterology.

Job DescriptionDescription: Lab Technician / Assistant Clinical Research Coordinator Location: Orlando, FL Job Type: Full-Time About Us APG Research, LLC is a rapidly growing clinical research site specializing in psychiatric and medical studies. We are seeking a Phlebotomy Pediatric and Adult / Lab Technician / Assistant Clinical Research Coordinator to support both laboratory and clinical trial operations. This role is ideal for a detail-oriented, patient-focused individual eager to contribute to advancing clinical research while ensuring high-quality study execution. Position Overview The Assistant Clinical Research Coordinator / Lab Technician will primarily be responsible for pediatric and adult phlebotomy and specimen processing, while also assisting with clinical research coordination tasks. This position works closely with the Principal Investigator (PI), research team, sponsors, and monitors to uphold the highest standards of study conduct. Requirements • Minimum 2 years of direct clinical research experience OR relevant laboratory/medical assistant experience with research exposure., • Strong phlebotomy skills (pediatric and adult) and specimen processing experience required., • Knowledge of clinical research protocols, regulatory compliance, and study documentation., • Medical Assistant degree or equivalent experience preferred., • SCRA or ACRP certification preferred (or willingness to obtain)., • Excellent organizational, communication, and multitasking skills., • Proficiency in Microsoft Office and clinical trial software (e.g., Medidata, Inform, Data Labs). Schedule: Monday–Friday Typical Hours: 8:30 AM – 5:30 PM (Monday–Thursday) and 8:30 AM – 3:00 PM (Friday) Key Responsibilities Laboratory & Phlebotomy (Primary Focus) • Perform phlebotomy for pediatric and adult study participants., • Process, label, and prepare biological specimens for shipment or analysis in accordance with study protocols., • Maintain accurate lab records, including temperature logs and chain of custody documentation., • Ensure compliance with GCP and laboratory safety standards., • Assist with informed consent collection and documentation., • Perform data entry, verification, and query resolution for Case Report Forms (CRFs)., • Support regulatory submissions (IRB documentation, deviation reporting)., • Assist with study start-up activities, including binder preparation, source document creation, and recruitment planning., • Monitor investigational product (IP) accountability and dispensation., • Review medical records to confirm eligibility criteria., • Support adverse event reconciliation and audit readiness., • Coordinate with monitors, sponsors, and CROs during site visits., • Opportunity to expand your skills in both laboratory and clinical research coordination., • Stable, on-site role with no travel required., • Be part of a collaborative and growing research team dedicated to advancing patient care.Requirements:

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 Bilingual Clinical Research Coordinators at our Winter Park, FL location! The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols while providing 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 hourly base compensation 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 • The Clinical Research Coordinator (CRC) obtains study participant informed consent., • Executes study protocol procedures in a detailed, organized, and professional manner., • Performs human specimen lab draws and processing, and packages specimen shipments., • Creates and completes study source documents and adverse event reporting on an e-source system., • Maintains study-specific files and supplies., • Communicate with the Study Sponsor/CRO regarding study-specific questions., • Participates in site visits from Sponsors/CROs, including site initiation and monitoring visits.QUALIFICATIONS, • Bachelor's degree preferred, but not required, • Phlebotomy experience is required, EKG or other patient labs/processes preferred, • Preferably 2+ years of experience as a Clinical Research Coordinator, • Familiar with e-source reporting via an electronic platform, • A clear understanding of ICH, FDA, and GCP regulations, • Impeccable organizational skills and attention to detail, • Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources, • An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven, • High-level critical thinking skills, • Working knowledge of medical terminology and lab collection/processing/storage procedures 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 MaUtapJvNy

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 Clinical Research Assistant at our Winter Park, FL location! The Clinical Research Assistant supports clinical research studies under the supervision of the Site Director or Clinical Research Coordinator. This role assists with clinic operations and study procedures across all phases of research, ensuring accurate data collection and compliance with GCP, IRB, and sponsor protocols while providing 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 hourly base compensation 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 • Assist with study procedures and patient visits according to protocol under the guidance of the Team Lead or CRC, • Document patient assessments, observations, and study data accurately and in compliance with GCP and protocol requirements, • Obtain and document informed consent following federal regulations and IRB guidelines, • Support patient recruitment efforts and scheduling to meet enrollment goals, • Maintain accurate source documentation and complete case report forms (CRFs), • Report adverse events to supervisors or investigators as needed, • Help manage study supplies, lab kits, and other trial materials, • Maintain confidentiality and follow all applicable compliance and ethical standards, • Communicate effectively with research team members and document relevant study communications, • Represent Flourish Research professionally in all interactions, • Perform additional duties as assigned by managementQUALIFICATIONS, • Associate degree in science or relevant clinical research experience required; Bachelor’s degree preferred, • 1–3+ years in clinical or biological research preferred, • Strong understanding of clinical research methods, • Effective collaboration across research teams, • Excellent written and verbal communication, • Proficiency in Microsoft Office 365, • High ethical standards and professionalism, • Strong work ethic with attention to detail and quality, • Technical skills such as ECG and phlebotomy, as required by protocol, • Adaptable and open to taking on additional tasks, • Supports departmental process improvements and training initiatives 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 IVEglqYdXu

Job Description Clinical Research Coordinator II Job Description The Clinical Research Coordinator plays a crucial role in managing all aspects of clinical research, including patient screening, eligibility assessment, and the coordination of care and follow-up for volunteers involved in research studies, trials, and programs. This role involves recruiting and consenting research participants for various therapeutic areas, providing exceptional service during patient interactions, and coordinating biospecimen collection in collaboration with clinical research nursing staff and laboratory teams. The coordinator ensures ongoing regulatory and protocol compliance through effective collaboration with hospital departments and research teams. Responsibilities • Execute and coordinate the informed consent process for research participants across multiple locations, which may involve traveling between sites or using technology., • Screen patients, assess eligibility, and coordinate the participation and follow-up of volunteers in research studies., • Recruit and consent research participants for therapeutic areas served., • Provide concierge-level service for all patient interactions during clinical trials and research studies., • Coordinate or perform biospecimen collection (e.g., blood, tissue) and maintain HIPAA-compliant databases connecting patient information to biospecimens used in research., • Collaborate with Clinical Research nursing staff, Research Services, laboratory teams, and hospital departments to ensure regulatory and protocol compliance., • Work with assistant clinical coordinators to ensure compliant data entry into registries, patient records, and research-specific database systems., • Assist Principal Investigators and research staff in developing compliant research protocols and control documents., • Serve as the study-specific point of contact for participants, investigators, research staff, hospital departments, and external research partners., • Collaborate with clinical research supervisors and staff to implement standard operating procedures (SOP) for the research division., • Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks effectively and timely., • Knowledge of HIPAA data protection and patient advocacy, or similar awareness of ethical treatment of research participants., • Effective communication skills with research participants, investigators, staff, and external partners., • Analytical problem-solving skills with sound judgment., • Adaptability to respond to changing needs in clinical research units., • Bachelor’s degree in Healthcare Administration, Research, or related field with no experience required., • Associate's degree in Healthcare Administration, Research, or related field with two years of experience., • Graduate of an accredited allied health certificate program with four years of clinical research or healthcare experience. Pay and Benefits The pay range for this position is $64480.00 - $70720.00/yr. Benefits from Day One Paid Days Off from Day One Career Development Whole Person Wellbeing Resources Mental Health Resources and Support Pet Insurance* Debt-free Education* (Certifications and Degrees without out-of-pocket tuition expense Workplace Type This is a fully onsite position in Orlando,FL. Application Deadline This position is anticipated to close on Oct 17, 2025. 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 COMPANY DESCRIPTION Charter Research is a highly experienced and quickly growing clinical research company, based in Florida and Illinois that is looking to add to our team to help us fulfill our mission of discovering future medicines. Our company is privately owned and prides itself on providing exceptional patient experience to our participants, as well as offering agile recruitment strategies to our sponsors. Above all, we are a team, and we are seeking the right team member to add to our foundation in Orlando. POSITION OVERVIEW The Clinical Research Coordinator is responsible for overseeing the day-to-day operations of clinical trials. The Clinical Research Coordinator plans and directs clinical research studies – working directly with patients to guide them successfully through the clinical trial process – and is responsible for managing clinical trial performance. Team Members in this role are expected to follow Good Clinical Practice (GCP) in the conduct of clinical investigations and to collect, record, and maintain source and sponsor documentation. RESPONSIBILITIES • Understand thoroughly all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator., • Adhere strictly to the study protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures, laboratory information, and other requirements., • Educate patients and their family members regarding the clinical trials process and the details of the specific study in which they’re participating., • Assess eligibility of potential patients and oversee patient enrollment to ensure that informed consent is properly obtained and documented., • Coordinate and conduct patient visits (drawing blood, collecting vital signs, performing ECGs, and processing specimens) and assure all procedures are conducted in compliance with the clinical trial protocol and Good Clinical Practice (GCP)., • Communicate clinical trial issues to Sponsor and/or Contract Research Organization (CRO), Principal Investigator, and Clinic Manager., • Keep all source documentation up-to-date and in compliance with ALCOA-C standards., • Communicate closely with the sponsor’s Clinical Research Associate (CRA) to facilitate the sponsor monitoring and data maintenance process., • Complete all monitor and sponsor queries in a timely manner., • Track enrollment status of patients and ensure timely communication with patients regarding their study participation., • Prepare for and/or participate in quality assurance audits conducted by study sponsors, federal agencies, or other review groups., • Excellent interpersonal and customer service skills., • Exceptional organizational skills and attention to detail., • Strong verbal and written communication skills., • Ability to work well both independently and as part of a team., • Ability to handle multiple tasks simultaneously and adapt to changes in responsibilities and workloads. Language Fluency in Spanish is required (Orlando location only). Education & Experience • Bachelor’s degree preferred., • Minimum 1 year of phlebotomy experience in a clinical, laboratory, or hospital setting preferred., • Prolonged periods of sitting at a desk and working on a computer., • Prolonged periods of standing, bending, and reaching.

Clinical Research Coordinator I (CRC I). Join our growing team as a Clinical Research Coordinator I, contributing to the execution of high-volume clinical trials in nephrology. Enthusiasm and commitment to patient safety and ethical research practices.

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.

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

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). Enthusiasm and commitment to patient safety and ethical research practices.

Clinical Research Coordinator II Job Description The Clinical Research Coordinator plays a crucial role in managing all aspects of clinical research, including patient screening, eligibility assessment, and the coordination of care and follow-up for volunteers involved in research studies, trials,

Our Lakeland, Florida office is looking for a talented Project Manager to join our team.In this role, you will get to manage and lead multi-discipline planning, design, and construction teams for water and wastewater collection, distribution, pumping, and treatment facilities.Lead and manage multi-d

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A top-tier general contractor specializing in complex builds like.We’re looking for someone sharp, driven, and curious—someone who thrives in a fast-paced environment and knows how to make smart decisions.Lead and manage construction projects from pre-construction through closeout, ensuring qual

Construction Project Manager – Restoration/Reconstruction.Since 1948, BMS CAT has been the trusted leader in disaster recovery.From emergency clean-up to complete reconstruction, we deliver for our clients on projects ranging from multi-million-dollar commercial losses to single-family residential

Norlee Group Company, is a blend of companies with capabilities that are unique in the construction industry.Services offered range from mechanical, electrical, and plumbing engineering design to turnkey electrical and mechanical engineering design and construction, to low voltage cabling system des

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

My Client, a Top ENR 50 Engineering, Environmental and Geotechnical firm with 40 offices USA wide, provides expert land development engineering and environmental consulting services for major developers, renewable energy producers, energy companies, corporations, healthcare systems, colleges/univers

Our Lakeland, Florida office is seeking a talented Senior Project Manager to join our team.In this role, you will get to manage and lead multi-discipline planning, design, and construction teams for water and wastewater collection, distribution, pumping, and treatment facilities.Lead and manage mult

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

Do you thrive on taking ownership of construction projects and seeing them through from concept to completion?.Project Manager to lead the day-to-day execution of luxury residential and commercial construction projects throughout the Florida.If you're someone who excels at managing budgets, timeline

Project Manager (with Estimating Development Path).This position offers a unique opportunity to manage active drywall projects while being mentored and developed into a dual role that includes estimating future work.The ideal candidate is detail-oriented, driven, and eager to grow their expertise in

Visium Resources has been asked to identify qualified candidates for this Project Manager role.We are currently seeking an experienced Civil Engineering Land Development Project Manager to assist with our client's continued project workload.This role provides an opportunity to work in a small office

Senior Project Manager - Land Development.Orlando, FL | Mid-Sized, Growth-Oriented Firm | Full-Time.Are you a seasoned land development professional with a passion for shaping large-scale communities? Do you thrive in a collaborative environment and aspire to grow into a leadership role? If so, we w

Commercial HVAC Project Manager.This role ensures that projects meet schedule commitments, stay within budget, and comply with all design specifications, safety requirements, and contractual obligations.Serving as the central communication hub, the Project Manager works closely with clients, interna

JTI is a growing, progressive, and team-oriented company rooted in family values.We know that our employees are our number one asset.We not only encourage, but foster an environment that promotes professional growth, internal promotions, continuing education, and a safe work environment.We are proud

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

We are seeking a highly skilled.The ideal candidate has hands-on experience in networking, systems, and data center technologies, with a career path that transitioned from.Healthcare industry experience is highly preferred.Collaborate with technical teams, vendors, and stakeholders to.Translate comp

DocCafe has an immediate opening for the following position: Physician Assistant - Academic/Faculty/Research in Florida.

Kavaliro is seeking a highly organized and adaptable.This role is focused on managing strategic integration projects, particularly involving mergers and acquisitions.The ideal candidate will thrive in a fast-paced environment and bring a strong background in project coordination, regulatory complian

Location: Orlando, FloridaJob Type: ContractCompensation Range: $80 - 86 per hourWe are seeking an exceptional Senior Project Manager to join us for a critical, high-visibility role that is essential to the digital commerce strategy of our major entertainment client!You will lead a high-stakes digit

Orlando, FL (Hybrid - 3 days a week in office).Lead end-to-end project execution across technical, product, and business domains using Agile and/or Waterfall methodologies.Manage delivery of web-based applications, ensuring scalable architecture and performance optimization.Oversee planning, trackin

Our client is seeking a Project Manager to join their team.This position is located in Orlando, Florida.Lead end-to-end program and project planning across multiple workstreams and disciplines.Develop and manage project schedules, communication strategies, and financial forecasts.Partner with Produc

Commercial Construction Project Manager position open in Orlando FL, Large-Scale Ground Up Projects.A leader in the Commercial Construction industry that provides an excellent opportunity for growth and high performance.Ability to successfully manage large scale projects and/or multiple projects sim

Optomi, in partnership with a leader in the Entertainment Industry is seeking a a Senior Technology Project Manager who will be responsible for leading large-scale, complex Ecommerce software development projects across multiple disciplines.The role blends program/project management, team leadership

Commercial Construction Assistant Project Manager position open in Orlando, FL.A leader in the Commercial Construction industry that provides an excellent opportunity for growth and high performance.As Assistant Project Manager, you will be responsible for the project costing, safety, scheduling, bu

Location: Orlando, FloridaJob Type: ContractCompensation Range: $75 - 85 per hourWe are seeking an experienced and self-directed Senior Project Manager to lead the infrastructure and DevOps strategy supporting the post-live production environment for our client's critical commerce applications.This

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

We are seeking a highly skilled.The ideal candidate has hands-on experience in networking, systems, and data center technologies, with a career path that transitioned from.Healthcare industry experience is highly preferred.Collaborate with technical teams, vendors, and stakeholders to.Translate comp

Remote Work From Home Administrative Assistant Admin - Part Time Market Research Panelists Our company is seeking individuals to participate in National & Local Paid Focus Groups, Clinical Trials, and Market Research assignments. Seeking participants for Focus Group and market research studies.

We are seeking a highly skilled.The ideal candidate has hands-on experience in networking, systems, and data center technologies, with a career path that transitioned from.Healthcare industry experience is highly preferred.Collaborate with technical teams, vendors, and stakeholders to.Translate comp

Construction Project Manager Public Works/Civil/Schools/Fire stations Projects.Our client specializes in delivering high-quality construction projects with a focus on K-12 schools, federal facilities, and government infrastructure.With a proven track record of excellence, they're committed to innov