Clinical Research Assistant

SCOPE & RESPONSIBILITIES:

• Support the clinical conduct and administration of clinical trials, primarily in Europe.

• Facilitate patient enrollment and assist in driving subject enrollment throughout clinical trials.

• Visit clinical sites to ensure satisfactory study progress and compliance with protocols.

• Ensure clinical data is complete, including image availability for the core lab.

• Assist in preparing clinical summaries and reports for various purposes, such as presentations, regulatory submissions, and publications.

• Perform other tasks and responsibilities as needed to support clinical trials.

• Report to the Chief Clinical Officer.

REQUIREMENTS:

• Bachelor’s Degree in Life Sciences (Nursing, Biology, Biotechnology, Biomedical Engineering, or a similar field).

• Experience in clinical trials and GCP (Good Clinical Practice).

• High level of English proficiency.

• Ability to travel frequently, primarily to Europe.

• Strong organizational and time management skills, with the ability to work independently and efficiently.

• Excellent verbal and written communication skills.

• Proficient in Microsoft Office (Word, Excel, PowerPoint) and electronic data capture platforms.

• Ability to maintain strong relationships and communication with clinical sites and research teams.