Clinical Research Coordinator II- AI & Human Health
About The Position
Under minimal supervision, coordinates the clinical assessments of the study subjects; analyzes and assists in interpreting moderately complex clinical research data. Prepares grant applications and documents and assists in protocol submissions (for e.g., Institutional Review Board, Grants and Contracts Office). The Clinical Research Coordinator II assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office). We are seeking a highly motivated and organized Clinical Research Coordinator II (CRC II) to join our research team. The CRC II will play a critical role in supporting two NIH-funded clinical research projects by focusing on patient recruitment, participant engagement, and coordination of study-related meetings. This position offers the opportunity to contribute to groundbreaking research while working closely with faculty investigators, research staff, and study participants
Requirements
- Bachelors degree in sciences or related field.
- 2 years of clinical research
Nice To Haves
- Prior experience in clinical research, patient recruitment, or healthcare setting (preferred).
- Familiarity with IRB processes, research ethics, and HIPAA compliance (preferred).
Responsibilities
- Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
- Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
- Prepares and ensures grant applications, IRB/GCO documents are submitted.
- Ensures accurate and complete compilation of subject data through chart reviews.
- Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials.
- Obtains informed consent under supervision of the Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects, and for studies involving genetic tests.
- Independently obtains informed consent for other clinical studies.
- Mentors Clinical Research Coordinators in training.
- Patient Recruitment & Enrollment Identify, screen, and recruit eligible patients into study protocols.
- Obtain informed consent in compliance with institutional and federal guidelines.
- Serve as a primary contact for participants, ensuring a positive research experience.
- Study Coordination Schedule and coordinate study-related meetings, including with investigators, study staff, and collaborators.
- Maintain accurate and timely study records, logs, and regulatory documentation.
- Assist with scheduling participant visits, follow-up calls, and reminders.
- Communication & Collaboration Act as a liaison between participants, investigators, and the research team.
- Coordinate with clinical and administrative staff to ensure smooth study operations.
- Performs other related duties.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
