Clinical Trial Coordinator/Patient Recruitment Manager
Listed on 2026-10-14
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Healthcare
Clinical Research
Clinical Research Actively Hiring Featured
Clinical Trial Coordinator / Patient Recruitment ManagerNew Port Richey, Florida
Full-time
Fresher, Experienced are welcom
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About HiringMusB Research is seeking a motivated and organized Clinical Trial Coordinator / Patient Recruitment Manager to support our growing clinical research programs. This position offers an exciting opportunity to work directly with patients, research teams, and study sponsors while contributing to innovative research in microbiome science, aging, metabolic health, and other emerging healthcare fields. We are looking for individuals who are passionate about advancing healthcare through research and delivering an exceptional participant experience.
ResponsibilitiesLead and manage participant recruitment and enrollment activities for clinical studies.
Serve as the primary point of contact for study participants, clients, sponsors, and research partners.
Coordinate clinical research activities in accordance with study protocols and regulatory requirements.
Maintain accurate study documentation, participant records, and research data.
Support communication between investigators, sponsors, regulatory agencies, and study teams.
Assist with data collection, inventory management, and research-related operational activities.
Monitor study progress and address participant or study-related inquiries.
Ensure timely reporting and resolution of protocol deviations and study issues.
Support administrative tasks necessary for successful study execution.
What You'll BringHigh school diploma or bachelor's degree in life sciences, healthcare, nursing, public health, or a related field.
Previous experience in clinical research, patient recruitment, healthcare coordination, nursing, or medical assistance preferred.
Strong organizational and communication skills.
Ability to manage multiple tasks and projects simultaneously.
Familiarity with clinical trial processes and regulatory requirements is preferred.
Proficiency with Microsoft Office and electronic data management systems.
Ability to work independently and collaboratively within a multidisciplinary team.
Weekend availability and flexible scheduling preferred.
What You Will GainCompetitive compensation.
Paid time off.
Wellness program.
Free parking.
Hands-on experience in innovative clinical research programs.
Supportive and collaborative work environment.
Opportunity to contribute to meaningful scientific discoveries that impact patient health.
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