What You'll Do:
- Enter clinical trial data into EDC systems with high accuracy and timeliness in accordance with protocols.
- Review source documents, perform quality checks, and resolve data discrepancies and queries promptly.
- Track timelines and support database lock activities, maintaining organized, audit-ready documentation.
What We're Looking For:
- High attention to detail, strong organizational skills, and ability to manage multiple studies and deadlines.
- Familiarity with clinical research processes, GCP guidelines, and effective communication in a remote environment.
- Proficiency in Microsoft Office and preferred experience with EDC systems or 1-3 years in clinical research data management.
Why Join Profound Research:
- Contribute meaningful impact by advancing medical knowledge and expanding therapeutic options for patients.
- Receive support for professional growth through comprehensive training, certification, and ongoing education.
- Work in a collaborative culture with a dedicated team and access a full benefits package including competitive compensation.
Profound Research
Profound Research partners with community physicians to offer clinical trials as a therapeutic option for their patients, handling all infrastructure and operations. It is a collaborative organization that invests in professional growth and offers competitive benefits.