About the role
Clinical Research Coordinator (Onsite | Monday–Friday)
Are you a passionate Clinical Research Coordinator looking to advance your career in oncology research? We're seeking a motivated, patient-focused professional to join a collaborative research team supporting innovative clinical trials that make a meaningful impact on patient care.
What You'll Do:
- Coordinate and manage day-to-day clinical trial activities from patient enrollment through study completion.
- Work directly with research participants, ensuring a positive patient experience while maintaining protocol compliance.
- Collaborate with physicians, nurses, sponsors, and multidisciplinary teams to support successful study execution.
- Maintain accurate study documentation and ensure compliance with GCP guidelines, human subjects protection, and regulatory requirements.
- Utilize EMRs, Microsoft Office, and research databases such as REDCap and CTMS to manage study data and documentation.
What We're Looking For:
- Bachelor's degree in a health-related field (biology, nursing, public health, or similar).
- Minimum of 2 years of onsite, patient-facing Clinical Research Coordinator experience.
- Strong understanding of clinical research processes, GCP guidelines, and regulatory requirements.
- Excellent organizational skills with strong attention to detail and communication abilities.
- Ability to thrive in a fast-paced, collaborative clinical research environment.
- Oncology research experience is highly preferred.
Schedule:
- Full-time, onsite
- Monday–Friday, 8:00 AM–5:00 PM
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