Job Summary
We are hiring a Clinical Research Coordinator II to support oncology clinical trials at a healthcare institution. This onsite role is ideal for someone with experience managing Phase I oncology studies, coordinating patient activities, maintaining regulatory compliance, and working closely with physicians and research teams.
Responsibilities
- Coordinate day-to-day activities for oncology clinical trials.
- Recruit and schedule study participants and maintain study documentation.
- Ensure compliance with HIPAA, FDA, GCP, and IRB requirements.
- Track study progress, manage data, and support regulatory submissions.
- Collaborate with investigators, sponsors, and clinical staff to ensure successful study execution.
Qualifications
- Bachelor's degree in a related field or equivalent experience.
- 2+ years of clinical research experience.
- Experience with oncology treatment trials, including Phase I studies.
- Experience using EPIC.
- Strong knowledge of HIPAA, FDA regulations, GCP, and IRB processes.
- Excellent communication and organizational skills.
Note: This position requires experience in a hospital or academic medical center. Candidates with only CRO or pharmaceutical CRA experience are not a match.
Pay: $44.82 - $51.72 per hour
Work Location: In person
