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.