Clinical Trial Associate

Clinical Trial Associate Cambridge Start Date: ASAP Competitive Compensation Package We are seeking a highly motivated and detail-oriented Clinical Trial Associate to join the growing team of one of our clients in Cambridge.
In this role, you will play a crucial part in ensuring the successful management of clinical trials.
You will be responsible for maintaining and managing Trial Master Files (TMFs), ensuring compliance with industry standards and regulatory requirements.
This is an exciting opportunity to contribute to the development of life-changing treatments
What will you be doing Manage and maintain Trial Master Files (eTMF & paper) ensuring accuracy and compliance.
Process, review, and quality check essential clinical trial documentation.
Assist with TMF migrations.
Conduct TMF audits and resolve discrepancies.
Collaborate with clinical trial teams and sponsors.
What do you bring to the table?
Proven experience as a Clinical Trial Associate.
Hands-on eTMF experience & understanding of TMF structures.
TMF migration experience is highly desirable.
In-depth knowledge of GCP and regulatory requirements.
Excellent organizational skills and attention to detail.
Veeva Vault experience is a plus.