A company is looking for a Clinical Research Coordinator to provide support for oncology clinical trials.
Key Responsibilities
- Educate physicians and research staff about clinical trials in the TIME program
- Screen potential study participants and manage patient tracking for trials
- Ensure timely data entry into electronic data capture systems and assist with trial activations
Required Qualifications
- Bachelor's degree in Life Sciences or a health-related field
- 2+ years of clinical research experience in an oncology setting
- Knowledge of FDA regulations and Good Clinical Practices (GCP)
- CCRC certification preferred
- Proficiency with EDC systems and MS Office applications
