Supervisor Clinical Research Coordinator, Clinical Trials, FT, 8:00A - 4:30P

Baptist Health is the region's largest not-for-profit healthcare organization, with 12 hospitals, over 29,000 employees, 4,500 physicians and 200 outpatient centers, urgent care facilities and physician practices across Miami-Dade, Monroe, Broward and Palm Beach counties. With internationally renowned centers of excellence in cancer, cardiovascular care, orthopedics and sports medicine, and neurosciences, Baptist Health is supported by philanthropy and driven by its faith-based mission of medical excellence. For 26 years, we've been named one of Fortune's 100 Best Companies to Work For, and in the 2025-2026 U.S. News & World Report Best Hospital Rankings, Baptist Health was the most awarded healthcare system in South Florida, earning 63 high-performing honors.

What truly sets us apart is our people. At Baptist Health, we create personal connections with our colleagues that go beyond the workplace, and we form meaningful relationships with patients and their families that extend beyond delivering care. Many of us have walked in our patients' shoes ourselves and that shared experience fuels our commitment to compassion and quality. Our culture is rooted in purpose, and every team member plays a part in making a positive impact - because when it comes to caring for people, we're all in.

At Baptist Health, we're committed to supporting our employees at every stage of their journey, both personally and professionally. Our approach is rooted in a "grow our own" philosophy, designed to help our team members build meaningful, long-term careers with us, supported by benefits that make a real difference, including:

• Career growth and development opportunities , with clear pathways and ongoing support
• Comprehensive health and wellness resources that go beyond traditional benefits
• A wellness program that can help employees eliminate their medical plan deductible , reducing out-of-pocket healthcare costs
• Tuition reimbursement to support continued learning and advancement
• And so much more

Together, these benefits and others reflect our commitment to caring for our people, so they can build fulfilling careers with us while making a meaningful impact every day.

Description

The Clinical Research Supervisor over sees daily supervision of clinical research staff and provides support to Research Manager / Director and Principal Investigator of designated research projects. He/she performs those functions required by the research protocols with attention to participant safety and ensures that all requirements of the research protocol are met. He/she assures compliance with regulatory standards for each protocol. Must be able to complete detailed paperwork in strict accordance with regulatory requirements and deal with physicians, patients, sponsors and other departments in a service excellence manner. Estimated salary range for this position is $83400.24 - $108420.31 / year depending on experience.

Qualifications:
The Clinical Research Supervisor over sees daily supervision of clinical research staff and provides support to Research Manager / Director and Principal Investigator of designated research projects. He/she performs those functions required by the research protocols with attention to participant safety and ensures that all requirements of the research protocol are met. He/she assures compliance with regulatory standards for each protocol. Must be able to complete detailed paperwork in strict accordance with regulatory requirements and deal with physicians, patients, sponsors and other departments in a service excellence manner. Estimated salary range for this position is $83400.24 - $108420.31 / year depending on experience.Degrees:

• Associates degree is required.

Licenses & Certifications:

• ACRP Certified Clinical Research Coordinator.

Additional Qualifications:

• Bachelors degree in health related field preferred.
• Bilingual (English/Spanish) preferred.
• Background in research methodology, a plus.
• Computer literacy in Microsoft Office and Electronic Capture Platforms.
• Ability to manage multiple projects/protocols systematically with multiple departments, physicians and research coordinators.
• Excellent interpersonal, collaborative, and team-building skills are required.
• Must be able to work in high-stress, high volume area and multi-task to ensure enrollment of patients in research protocols according to regulatory requirements.
• Excellent interpersonal, collaborative and team-building skills.
• Ability to travel throughout BHSF entities on a weekly basis.

Minimum Required Experience: 5 YearsDegrees:

• Associates degree is required.

Licenses & Certifications:

• ACRP Certified Clinical Research Coordinator.

Additional Qualifications:

• Bachelors degree in health related field preferred.
• Bilingual (English/Spanish) preferred.
• Background in research methodology, a plus.
• Computer literacy in Microsoft Office and Electronic Capture Platforms.
• Ability to manage multiple projects/protocols systematically with multiple departments, physicians and research coordinators.
• Excellent interpersonal, collaborative, and team-building skills are required.
• Must be able to work in high-stress, high volume area and multi-task to ensure enrollment of patients in research protocols according to regulatory requirements.
• Excellent interpersonal, collaborative and team-building skills.
• Ability to travel throughout BHSF entities on a weekly basis.

Minimum Required Experience: 5 Years