Clinical Research Coordinator

Mayo Clinic • Jacksonville, FL

221d • $27 - $41 • Onsite

About The Position

Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & World Report. As we work together to put the needs of the patient first, we are also dedicated to our employees, investing in competitive compensation and comprehensive benefit plans - to take care of you and your family, now and in the future. And with continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic.

Requirements

• HS Diploma with at least 5 years of clinical research coordination/related experience OR Associate's degree/college Diploma/Certificate Program with at least 3 years of experience, Associate's in Clinical Research from an accredited academic institution without experience OR Bachelor's with at least 1 year of experience or completion of a Mayo Clinic-sponsored clinical research internship in lieu of 1 year of experience.
• Experience should be in the clinical setting or related experience.

Nice To Haves

• Graduate or diploma from a study coordinator training program is preferred.
• One year of clinical research experience is preferred.
• Medical terminology course is preferred.
• Completion of a Mayo Clinic Orthopedic Research Internship preferred.

Responsibilities

• Receives direction from principal investigator, supervisor, or other staff involved in research protocol(s).
• Gives direction to and works cooperatively with other research staff.
• Collaborates with various departments within the institution.
• Works cooperatively with other investigators and personnel at all levels.
• Interacts with research participants, other research centers, and sponsoring companies to resolve problems and ensure efficient completion of research studies.
• Independently coordinates complex clinical research protocols with minimal direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines.
• Collaborates with research team to assess feasibility and management of research protocols.
• Ensures implementation of research protocols after IRB approval and provides information as appropriate for progress reports.
• Screens, enrolls, and recruits research participants.
• Coordinates schedules and monitors research activities and subject participation.
• Identifies, reviews, and reports adverse events, protocol deviations, and other unanticipated problems appropriately.
• Manages, monitors, and reports research data to maintain quality and compliance.
• Provides education/training for others within the department.
• Performs administrative and regulatory duties related to the study as appropriate.
• Ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics, and verification of content to meet institutional and federal standards.
• Communication with study sites and/or federal agencies regarding study status changes.
• Federal and Institutional Review Board (IRB) document preparation and submission.
• Provides consultative expertise regarding regulatory and policy requirements.
• Accurately applies investigators' scientific data into a cohesive format for the protocol document and associated procedures that are consistent with internal and external policies and regulatory requirements.
• Participates in other protocol development activities and executes other assignments as warranted and assigned.

Benefits

• Medical: Multiple plan options.
• Dental: Delta Dental or reimbursement account for flexible coverage.
• Vision: Affordable plan with national network.
• Pre-Tax Savings: HSA and FSAs for eligible expenses.
• Retirement: Competitive retirement package to secure your future.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Hospitals
• Education Level: High school or GED