Clinical Research Coord 3, MCVI Research, FT, 8A-4:30P

Baptist Health; Miami (FL); On-site; USD 44,248 - 57,528; Full time

Benefits offered by this job

Career growth opportunities

Health and wellness resources

Tuition reimbursement

Wellness program to offset deductible

Job summary

Baptist Health in Miami seeks a Clinical Research Coordinator to support the Research leadership and Principal Investigator on a designated project. You will ensure protocol requirements are met, maintain safety, and collaborate with physicians, patients, sponsors, and departments in a service-driven environment.

The role requires mentoring junior CRCs and RAs, managing multiple protocols, and delivering detailed regulatory paperwork in line with FDA requirements.

Qualifications

• Bachelor's degree required; BA acceptable.
• CITI and clinical research certifications required.
• Extensive experience in all aspects of Clinical Trials.
• Strong verbal and written communication skills.

Responsibilities

• Support Research leadership and Principal Investigator.
• Ensure protocol compliance with regulatory standards and FDA requirements.
• Mentor junior CRCs and RAs.
• Manage multiple protocols concurrently.

Skills

Interpersonal skills

Communication

Team-building

Organization

Education

Bachelor's degree

Tools

Microsoft Office

Job description

Benefits

• 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

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. He/she will be expected to manage multiple protocols simultaneously. Serves as a mentor to junior CRC‘s and RA‘s. Estimated pay range for this position is $32.12 - $41.76 / hour depending on experience.

Qualifications

Degrees:

• Bachelors.

Licenses & Certifications:

• Basic Life Support.
• ACRP Certified Clinical Research Coordinator.
• SOCRA Certified Clinical Research Professional.
• Collab Inst Training Init.

Additional Qualifications

• Bachelor of Arts - BA required.
• In lieu of Bachelor‘s degree, Associates degree with 6 years of research experience OR a Foreign Medical Degree with 2 years of experience required.
• CITI and CCRC/CCRP/SOCRA certifications are required.
• Extensive experience in all aspects of Clinical Trials.
• 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 in meeting deadlines.
• Strong verbal and written communication skills.

Minimum Required Experience: 4 Years

EOE, including disability/vets