Job Description

Baptist Health is the region's largest not-for-profit healthcare organization, with 12 hospitals, over 28,000 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 25 years, we've been named one of Fortune's 100 Best Companies to Work For, and in the [click to reveal phone number]2024-2025 U.S. News & World Report Best Hospital Rankings, Baptist Health was the most awarded healthcare system in South Florida, earning 45 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 out 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.

Description

Responsible for supporting the Research leadership and Principal Investigator of a designated research project. Performs those functions required by the research protocols with attention to participant safety. Ensures that all requirements of the protocol are met, while meeting compliance with regulatory standards and FDA requirements for each protocol. Must be able to complete detailed paperwork in strict accordance with regulatory requirements and collaborate with physicians, patients, sponsors, and other departments in a service excellence manner.

Qualifications:
Responsible for supporting the Research leadership and Principal Investigator of a designated research project. Performs those functions required by the research protocols with attention to participant safety. Ensures that all requirements of the protocol are met, while meeting compliance with regulatory standards and FDA requirements for each protocol. Must be able to complete detailed paperwork in strict accordance with regulatory requirements and collaborate with physicians, patients, sponsors, and other departments in a service excellence manner.Degrees:

• Associates degree is required.

Licenses & Certifications:

• Collab Inst Training Init.
• Basic Life Support.

Additional Qualifications:

• Associates degree is required.
• In lieu of a degree, three years of research experience is required, or a foreign medical degree with one year of experience is required.
• Advanced computer literacy in Microsoft Office.
• Proven ability to manage multiple assignments systematically.
• Excellent interpersonal, collaborative, and team-building skills are required.
• Must be able to work in a high-demand environment with the ability to take responsibility for meeting deadlines.
• Strong verbal and written communication skills.
• CCRC/CCRP certification preferred.

Minimum Required Experience: 2 yearsDegrees:

• Associates degree is required.

Licenses & Certifications:

• Collab Inst Training Init.
• Basic Life Support.

Additional Qualifications:

• Associates degree is required.
• In lieu of a degree, three years of research experience is required, or a foreign medical degree with one year of experience is required.
• Advanced computer literacy in Microsoft Office.
• Proven ability to manage multiple assignments systematically.
• Excellent interpersonal, collaborative, and team-building skills are required.
• Must be able to work in a high-demand environment with the ability to take responsibility for meeting deadlines.
• Strong verbal and written communication skills.
• CCRC/CCRP certification preferred.

Minimum Required Experience: 2 years

Job Tags

Full time, Work at office,

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