Clinical Research Coordinator
3 weeks ago
Overview: We are seeking an experienced and detail-oriented Clinical Research Coordinator (CRC) with at least 2 years of experience in clinical research. The ideal candidate will have experience in therapeutic areas such as NASH (Non-Alcoholic Steatohepatitis), Obesity, Cancer, or CNS (Central Nervous System) disorders.
Key Responsibilities:
- Coordinate and manage clinical trials from start-up to close-out, ensuring compliance with study protocols and regulatory requirements.
- Screen, recruit, and enroll study participants, ensuring eligibility criteria are met.
- Conduct study visits and procedures, collect data, and maintain accurate documentation.
- Monitor participant safety and report any adverse events according to protocol and regulatory guidelines.
- Communicate effectively with study participants, investigators, and the research team.
- Assist in the preparation of study-related documents, including informed consent forms, case report forms, and study protocols.
- Manage study supplies, laboratory samples, and investigational products.
- Ensure timely data entry and query resolution in clinical databases.
- Collaborate with other departments and external stakeholders to ensure the smooth execution of trials.
Qualifications:
- Bachelor’s degree in a related field (e.g., life sciences, nursing, psychology).
- At least 2 years of experience as a Clinical Research Coordinator or in a similar role.
- Experience in NASH, Obesity, Cancer, or CNS disorders is highly preferred.
- Knowledge of Good Clinical Practice (GCP) and regulatory requirements.
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