Clinical Research Coordinator- Generalist Pod

Mayo Career Site US; Jacksonville (FL); On-site; USD 65,000 - 90,000; Full time

Job summary

Mayo Clinic in Jacksonville, FL seeks a clinical research professional to coordinate complex interventional protocols with minimal supervision. You will collaborate across departments to ensure regulatory compliance and high-quality data, while managing participant screen/enrollment and study logistics.

Responsibilities include adverse event reporting, protocol maintenance, and education for the team. Some travel may be required as part of this role.

Qualifications

• Coordinate complex clinical research protocols with minimal supervision.
• Ensure compliance with regulatory laws and institutional guidelines.
• Screen, enroll, and recruit research participants.

Responsibilities

• Independently coordinates complex research protocols with minimal direction.
• Collaborates with research team to assess feasibility and manage protocols.
• Screens and enrolls participants, coordinates schedules and monitors activities.
• Identifies adverse events and protocol deviations and reports appropriately.

Skills

Clinical coordination

IRB knowledge

Regulatory compliance

Job description

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.

Position Overview: (Major Functions and Non-Essential Functions):
Independently coordinates complex (i.e. interventional, therapeutic greater than minimal risk) 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. Some travel may be required.

Protocol Development and Maintenance Activities Responsibilities may include, but are not limited to: ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics (i.e. blood collection kits, data collection booklets, use of CRU, etc.), 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; and 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.

Preferred candidates will have patient care experience and clinical research experience. This position will support various departments within: GI, Surgery, Transplant, Radiology.

Please note that visa sponsorship is not available for this position.