Clinical Trial Associate
- Provide administrative support to clinical study teams across multiple trials
- Maintain and update Trial Master Files (TMFs) in accordance with regulatory standards.
- Assist with ethics submissions, investigator site files, and essential document tracking.
- Support meeting preparation, minutes, and follow-ups.
- Coordinate with CROs, vendors, and internal stakeholders.
- Ensure adherence to GCP, SOPs, and company quality standards.
- Proven experience working as a CTA or in a similar role within the Life Sciences sector
- Strong understanding of clinical trial processes and regulatory guidelines (ICH-GCP)
- Exceptional organizational and multitasking skills
- Excellent written and verbal communication
- Proficient in Microsoft Office Suite and clinical trial management systems (CTMS, eTMF)
- Ability and commitment to work from the West London office at least 2 days per week
- Opportunity to work on cutting-edge clinical research projects
- Career progression and professional development support
- Collaborative and inclusive team environment
- Competitive salary and comprehensive benefits package
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