Senior Research Coordinator

Summary The Senior Research Coordinator independently coordinates and manages complex clinical research studies primarily within the Renal and Endocrine Divisions, ensuring compliance with federal regulations, sponsor requirements, institutional policies, and Good Clinical Practice (GCP) guidelines. Responsibilities include participant recruitment, study implementation, regulatory oversight, data management, sponsor communication, and study closeout. The position functions with a high degree of autonomy while supporting investigators and advancing the division's clinical research mission.

Job Duties Independently manages multiple complex therapeutic and interventional clinical research studies primarily within the Renal and Endocrine Divisions, including study start-up, participant enrollment, protocol execution, and regulatory compliance. Provides feasibility and operational recommendations to Principal Investigators and Research Managers, while serving as a mentor and resource to research staff and ensuring adherence to protocol, regulatory, and institutional requirements.

Screening & Enrollment – 20%
Screens, recruits, and enrolls patients/participants into complex clinical research studies in accordance with approved protocols.

Conducts participant interviews and verifies eligibility based on comprehensive inclusion and exclusion criteria.

Educates participants on study purpose, procedures, risks, and requirements and conducts the informed consent process in compliance with GCP and institutional policies.

Exercises independent judgment in evaluating participant eligibility and protocol compliance.

Supports study feasibility assessments through evaluation of patient populations, protocol requirements, staffing resources, and operational workflows.

Subject Visits – 30%
Provides study-specific education to research participants within scope of practice.

Reviews study protocols with participants and verifies informed consent documentation prior to study activities.

Schedules participants for protocol-required tests and procedures, including laboratory assessments and study-specific evaluations.

Dispenses investigational products in accordance with protocol requirements, institutional policies, and applicable regulatory standards while maintaining complete drug accountability records.

Collects, processes, stores, and ships biological specimens in accordance with protocol requirements, laboratory manuals, and IATA guidelines.

Monitors participants throughout study participation and ensures participant safety, rights, and welfare are maintained.

Identifies, documents, and facilitates reporting of adverse events, serious adverse events, and protocol deviations in accordance with protocol requirements and regulatory timelines.

Data Collection & Entry – 20%
Collects, documents, and records study-related data in collaboration with Principal Investigators, physicians, advanced practice providers, research nurses, and data managers.

Obtains participant information through direct interviews, questionnaires, and medical record abstraction; enters data into case report forms and electronic data capture systems.

Maintains accurate source documentation, study records, and essential study files to ensure compliance with regulatory requirements.

Ensures the accuracy, completeness, and scientific integrity of study data through ongoing review and quality oversight.

Assists with study monitoring visits, audits, and inspections as required.

Job Duties Source Document Development & Review – 15%
Prepares and maintains documentation required for initial and continuing regulatory approval of assigned research protocols.

Oversees the development, organization, quality review, and maintenance of study source documents and…