Clinical Research Coordinator I | Clinical Research Coordinator I (m/w/d) - Deutschland
Velocity Clinical Research Germany GmbH Berlin
Job Summary
As a Clinical Research Coordinator I at Velocity, you will play a pivotal role in the execution and management of clinical trials within the European Clinical Operations team. Your day-to-day responsibilities involve coordinating study protocols in strict adherence to Good Clinical Practice (GCP) and Standard Operating Procedures (SOPs). This includes managing subject recruitment, conducting patient visits, performing clinical tasks such as phlebotomy and ECGs, and ensuring accurate data entry into sponsor portals. You will act as a central point of communication between physicians, sponsors, and Contract Research Organizations (CROs). This position is ideal for detail-oriented professionals who thrive in fast-paced environments and are passionate about making clinical research more accessible. The role offers a dynamic international environment with flat hierarchies and the opportunity to work at the forefront of medical innovation, ensuring patient safety and data integrity across diverse clinical protocols.
Required Skills
Education
Bachelor's degree in Life Sciences, or High School Diploma/Technical Degree with equivalent professional experience.
Experience
- 1 year of relevant experience in the Life Science industry with a Bachelor's degree
- 3 years of relevant experience in the Life Science industry with a high school diploma or technical degree
- Professional experience in managing clinical trial protocols and regulatory documents
- Experience in patient screening and recruitment strategies
- Experience in clinical data entry and query resolution
Languages
Additional
- Must be able to perform clinical tasks including medication preparation, Fibroscans, and phlebotomy. Requires flexibility for rapid schedule changes and the ability to work in a fast-paced environment.