DescriptionThe Clinical Research Coordinator 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).
Responsibilities- Collects and records study data. Inputs all information into database.
- Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
- Assists in the activities related to clinical research studies including but not limited to: answering phone calls screening participants for eligibility registering subjects with sponsoring agency administering lifestyle questionnaires.
- Assists in preparing grant applications IRB/GCO for submission and filings.
- Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews.
- Secures delivers and ships clinical specimens as required by the protocol.
- Prepares for monitoring visits.
- Performs other related duties.
Qualifications- Bachelors or Masters degree in Science or closely related field.
- 1-2 years of research experience
Required Experience:
IC