Patient Recruitment Manager (Clinical Research)
Forcare-Clinical-Research
Patient Recruitment Manager (Clinical Research) Job Category : Recruitment Requisition Number : PATIE004327 Posted : September 4, 2026 Full-Time Locations Showing 1 location CenExel FCR 15416 N. Florida Ave. 101 Tampa, FL 33613, USA Description About Us: Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k. Job Summary: The Patient Recruitment Manager will be responsible for creating programs and solutions to support clinical trial recruitment and retention. Essential Responsibilities and Duties: Communicates and reaches out to referral connections, sponsors, or potential providers. Acts as the liaison for outside referring sources. Trains new staff members in the department. Identifies strategies to improve patient enrollment in research protocols in collaboration with Principal Investigator and/or site leadership. Supervises Recruitment Specialists and oversees recruitment department. Determines study support required for trials and understand enrollment needs and timelines of trials. Develops pre-screen scripts for new studies. Evaluates enrollment process to ascertain if current process recruits optimal study participant population. Conducts outreach and special events as needed and conducts presentations to various referral sources. Hires, trains, supervises, and evaluates personnel. Champions and enforces the strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site Working Practices, protocol, and company guidelines and policies. Retrains and implements corrective and preventative actions, as needed. Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive. Education/Experience/Skills: Able to effectively communicate verbally in both English and Spanish preferred . Bachelor's Degree or equivalent experience preferred. Knowledge of sponsors/study requirements and participant evaluation procedures. Understanding of clinical protocols Phase I to Phase IV. Skill in organization and record maintenance. Ability to work independently as well as functioning as part of a team. Must be self-directed and able to work with minimal supervision. Able to take a flexible approach to shifting priorities. Able to manage multiple projects and responsibilities. Motivated to work consistently in a fast paced and rapidly changing environment. Working Conditions Indoor, Office environment. Essential physical requirements include sitting, typing, standing, and walking. Lightly active position, occasional lifting of up to 20 pounds. Reporting to work, as scheduled, is essential. On site work arrangement. CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status. Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor. #J-18808-Ljbffr Forcare-Clinical-Research
$98.34k - $150.03k
...the Tampa Bay Times’ Top Workplaces. Summary The Assistant Patient Care Manager is responsible for the day-to-day supervision of nursing operations... ...a resource, and provides support for staff and faculty on clinical nursing issues while meeting the department, nursing, and...SuggestedWork at office- The University of South Florida in Tampa, FL seeks a Clinical Research Coordinator I to oversee screening, enrollment, and retention of study participants and to ensure high-quality data collection across clinical research projects. Under supervision of lead coordinators...Suggested
- ...Medical Director, Clinical Research Location: Tampa, Florida Relocation Assistance Available Position Overview A leading clinical... ...to obtain Florida licensure. Strong clinical trial management, oversight, or investigator experience. Strong knowledge...SuggestedFull timeLocal areaRelocation package
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- ...Job Description The Clinical Research Coordinator I is responsible for coordinating and performing research related activities for clinical... ...moderate in complexity at the site level. • Performs patient clinical assessments for clinical trial visits for assigned...SuggestedContract workWork experience placementMonday to Friday
- ...At K2 Medical Research, we are transforming healthcare by delivering... ...today. As a rapidly growing clinical research organization across... ...in clinical excellence and a patient-first mission. We are seeking... ...This position will manage clinical trial performance and...Full timeImmediate startMonday to ThursdayShift workWeekend work
- ...dignity, respect, responsibility, and clinical excellence. Title: Clinical Research Coordinator Facility: St.... ...protocol and schedule of events, patient visit scheduling for protocol... ...procedures Screening Study recruitment Preparation of IRB reports...Full timeShift workWeekend work
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- EPM Scientific is seeking an experienced Medical Director to lead medical operations at an established clinical research site in Tampa. The role provides site-wide medical leadership across an active portfolio of industry-sponsored trials and ensures participant safety,...
- ...Surgery Associates, LLP is seeking a Clinical Research Coordinator to drive orthopaedic... ...work with physicians and staff to recruit, coordinate, and analyze data... ...The role involves IRB submissions, patient education, data management, and preparing reports; you will collaborate...
- BayCare Health System is seeking a Supervisor Research - Cardiology at St. Joseph's Hospital in Tampa. You will oversee a portfolio of clinical trials and Research Nurse Coordinators to support Principal Investigators within the Cardiology service line. The role involves...
- ...Health System in Tampa, FL seeks a Clinical Research Coordinator to lead trials under... ...supports protocol development, recruitment, data collection, and regulatory... ...documentation, contributing to high-quality patient care. The coordinator will manage informed consent, site training,...
- ...Clinical Research Coordinator III Location: Tampa, FL Job Type: Full-Time About... ...ownership of study execution, drive patient recruitment and enrollment, and serve as a resource... ...improve recruitment and study workflows, manage multiple studies and a high volume of...Full timeLocal areaNight shift
- Moffitt Cancer Center is seeking a Clinical Research Coordinator to engage with patients, enroll them in clinical trials, educate families, and ensure protocol... ...with physicians, pharmacists, nurses, and data managers to move trials forward safely. The role offers a Monday...Monday to Friday
- Moffitt is seeking a Clinical Research Coordinator I to support myeloma/lymphoma trials. You will interact with patients, enroll and educate them in clinical trials, and ensure study progress safely and on plan. The role offers a Monday-Friday schedule with hybrid work...Monday to Friday
- Moffitt is seeking a Clinical Research Coordinator I to support patient care, enrollment, and trial coordination in a dynamic cancer research environment. Work involves interacting with patients and study teams to ensure protocol adherence and data integrity across trials...Relocation packageMonday to Friday
- Moffitt Cancer Center in Tampa is seeking a Clinical Research Coordinator II to support investigators in running cancer trials. You will screen, enroll and follow study subjects, educate patients, and help ensure protocol compliance while coordinating with physicians, nurses...
- Moffitt Cancer Center in Tampa is seeking a Clinical Research Coordinator I to support patient care, enrollment and study management in a dynamic research team. You will work with physicians, nurses and sponsors, ensure protocol adherence, document data, and participate...Relocation package
$26.32 - $40.14 per hour
## CLINICAL RESEARCH COORDINATOR I - Immune Cell TherapyApply: Onsite: Magnolia Hospital: Full time... ...Coordinator, you’ll bring hope to patients by delivering tomorrow’s cancer treatments... ..., nurses, data monitors and data managers. Position Highlights:• Coordinate patient...Full timeWork at officeRemote workRelocation packageMonday to Friday- Moffitt Cancer Center in Tampa, FL, is seeking a Clinical Research Coordinator to enroll and educate patients in therapeutic clinical trials, ensuring safe, compliant progress of studies. You will interact with patients and staff, schedule visits, and maintain trial documentation...Relocation package
- K2 Medical Research in Tampa, FL is seeking an experienced Clinical Research Coordinator to support ongoing trials and ensure adherence to GCP and sponsor SOPs. The role involves source documentation, patient interviews, and coordination with investigators and CROs. Ideal...
- Panoramic Health in Tampa, FL is seeking a Clinical Research Coordinator III to lead site-level... ...You will own study execution, drive patient recruitment and enrollment, and mentor junior... ...quality, compliant study conduct. You will manage multi-study workflows, ensure...
- Description The Clinical Research Coordinator manages orthopaedic research studies from planning through completion... ...to coordinate study activities, recruit participants, manage and analyze... ...documents, and renewals. Screen patients for study eligibility, coordinate informed...Local area
- Moffitt Cancer Center is seeking a Clinical Research Coordinator to support clinical trials by coordinating research activities and ensuring protocol compliance. You will interact with patients, enroll and educate them, and guide them through the trial experience, contributing...Relocation packageMonday to Friday
- Alcanza Clinical Research is seeking a Clinical Research Coordinator to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA regulations and SOPs. You will screen patients for enrollment, obtain informed consent, schedule visits, collect data...
$29.05 - $44.28 per hour
## Clinical Research Coordinator IIApply: Hybrid (Part -time in Office): Clinical Support Building... ...protocols, the CRC II will coordinate patient care by collaborating with medical... ...the use of EMR systems, clinical trial management systems and other various data capture...Full timePart timeWork experience placementWork at office- Moffitt is seeking a Clinical Research Coordinator I to advance cancer clinical trials. The role involves coordinating patient care, screening and enrolling subjects, and ensuring protocol compliance under supervision. You will work in a hybrid, Monday-Friday schedule with...Monday to Friday
- ...development, coordination and implementation of research and administrative strategies essential to the management of clinical trials research. This employee would support... ...Blvd., Suite C, Tampa, FL The majority of patient activity occurs at the Wesley Chapel location...
- ...growing multi-site, multi-phase clinical research company with a network of... ...limited to: Screening of patients for study enrollment;... ...documentation; May assist with study recruitment, patient enrollment, and... ...with co-workers, subjects, managers and external customers....Full timeTemporary work
- Moffitt Cancer Center in Tampa seeks a Clinical Research Coordinator I to support immune cell therapy trials and engage with patients throughout enrollment and treatment. You will help ensure trials run safely, smoothly, and on schedule under a mentor. A bachelor’s degree...Relocation package
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