Clinical Research Coordinator I - Health Equity Research Studies
About The Position
The Clinical Research Coordinator I 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). The CRC I will, under minimal supervision, coordinate the implementation of a clinical research study with community sites. This includes coordination of New York Community Engagement Alliance (NYCEAL) efforts across our Building Community Resilience Program (BCRP) and Food for Living, Access to Systems and Supportive Strategies for Health Equity (FLASH) interventions.
Requirements
- Bachelors or Masters degree in Science or closely related field.
- No experience required.
Nice To Haves
- One year of research experience preferred.
Responsibilities
- Collects and records study data.
- Inputs all information into database.
- Assist in monitoring and interpreting moderately complex clinical research data, prepare grant reports and other grant related documents, including contracts with community-based partners, and assists in protocol submissions, modifications, and reports (for e.g., Institutional Review Board, Grants and Contracts Office).
- Regularly liaise with representatives from community-based organizations, supporting community-based leaders and program participants in participating in our research programs and efforts.
- 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.
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What This Job Offers
Career Level
Entry Level
