Senior Clinical Trial Assistant

The Senior Clinical Trial Assistant provides essential opera
Senior Clinical Trial Assistant
The Senior Clinical Trial Assistant provides essential operational and administrative support across all phases of clinical studies. This role ensures high-quality documentation, compliance with regulatory standards, and smooth collaboration across internal and external stakeholders.
Senior Clinical Trial Assistant
Our client is a leading organization in clinical research and innovation, operating at the forefront of science and health.
They offer a dynamic and international working environment focused on excellence and continuous improvement.
Description
Support Clinical Project Managers in tracking study milestones and deliverables
Maintain and oversee Trial Master File (TMF/eTMF) completeness and quality
Prepare, review, finalize, and distribute clinical study documentation
Participate in study meetings, take minutes, and monitor follow-up actions
Coordinate investigator and vendor payments in collaboration with stakeholders
Assist in contract and budget tracking under supervision
Develop and maintain trackers, tools, and reports for study monitoring
Ensure accurate tracking of training records for study teams and site staff
Collaborate with CROs, vendors, and investigator sites to support study execution
Contribute to process improvement initiatives and documentation standards
Profile
Bachelor's degree in life sciences, healthcare, or a related field
Minimum 4 years' experience as a CTA in pharmaceutical, biotech, or CRO settings
Strong knowledge of ICH-GCP guidelines and clinical trial lifecycle
Experience with eTMF systems and TMF Reference Model
Exposure to outsourced clinical study models or vendor oversight
Excellent organizational and documentation management skills
Strong attention to detail with the ability to manage multiple priorities
Effective communication and stakeholder management capabilities
Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook)
Proactive, solution-oriented mindset with strong accountability
Fluency in English (written and spoken)
Job Offer
Opportunity to work in a fast-paced, international clinical research environment
Exposure to innovative projects and cross-functional collaboration
12-month full-time contract with engaging and expert people jidc01cae6afr jit0521afr jpiy26afr