Clinical Trial Coordinator / Patient Recruitment Manager

MusB Research; Florida; On-site; USD 52,000 - 66,000; Full time

Job summary

MusB Research is actively hiring a Clinical Trial Coordinator / Patient Recruitment Manager in New Port Richey, Florida. The role is full-time and welcomes both fresh graduates and experienced candidates. Apply by 2026-12-31.

The position focuses on leading participant recruitment, coordinating study activities, and ensuring regulatory compliance while delivering quality participant experiences within microbiome-related clinical research projects.

Qualifications

• High school diploma or bachelor's degree in life sciences, healthcare, nursing, public health, or 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 preferred.

Responsibilities

• Lead 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.

Skills

Organizational skills

Communication skills

Clinical research coordination

Regulatory knowledge

Microsoft Office

Electronic data management systems

Education

High school diploma

Bachelor's degree in life sciences/healthcare/public health

Tools

Microsoft Office

Electronic Data Capture/EDC systems

Job description

Clinical Research Actively Hiring Featured

Clinical Trial Coordinator / Patient Recruitment Manager

New Port Richey, Florida

Full-time

Fresher, Experienced are welcom

Apply By 2026-12-31

About Hiring

MusB 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.

Responsibilities

Lead 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 Bring

High 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 Gain

Competitive 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.