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Clinical Research Coordinator
2 months ago
We are seeking a highly skilled and detail-oriented Clinical Research Coordinator to join our team at OHC. As a key member of our Clinical Trials team, you will play a critical role in supporting the development and implementation of clinical research studies in oncology.
Key Responsibilities- Screen potential patients for protocol eligibility and present trial concepts and details to patients, participating in the informed consent process and enrolling patients on clinical trials.
- Assist with patient care in compliance with protocol requirements, including disbursing investigational drug and maintaining investigational drug accountability.
- Participate in data collection, entry, and reporting for subjects, and collaborate with physicians to review patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug, and thoroughly document all findings.
- Participate in required training and education programs, as well as monitoring and auditing activities, and may work directly with sponsors.
- Assist with collection and maintenance of regulatory documents in accordance with USOR SOPs and applicable regulations.
- Associate's degree in a clinical or scientific related discipline required, Bachelor's degree preferred.
- One year of experience in a clinical or scientific related discipline, preferably in oncology preferred.
- Excellent communication, organizational, and time management skills, with the ability to multi-task and work in a fast-paced environment.
- Strong attention to detail and ability to maintain confidentiality.
- A competitive salary and benefits package, including health insurance, dental and vision insurance, 401(k) plan, and profit sharing.
- A generous PTO plan and opportunities for professional development and advancement.
- A dynamic and supportive work environment with a team of experienced professionals.