At a Glance
- Tasks: Process and review TMF documents, ensuring quality control for regulatory compliance.
- Company: Join a leading clinical trials organisation dedicated to trial integrity.
- Benefits: Competitive salary, supportive team environment, and opportunities for professional growth.
- Other info: Collaborative culture with a focus on career advancement.
- Why this job: Make a difference in clinical trials while developing your skills in a dynamic field.
- Qualifications: Life sciences degree and 2-3 years of TMF experience preferred.
The predicted salary is between 27000 - 33000 £ per year.
Worldwide Clinical Trials is seeking a TMF Operations Analyst to join our Records Management Compliance team in the UK.
You will process, review and resolve TMF documents, ensure quality control, and work across electronic and hard copy formats to support regulatory compliance and trial integrity.
Ideal candidates have a life sciences degree, up to 2-3 years TMF experience in CRO/Pharma, and strong data handling, communication and organizational skills, with proficiency in Word and Excel.
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TMF Operations Associate II: Approvals & QC employer: Worldwide Clinical Trials
Worldwide Clinical Trials is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals passionate about clinical research. With a strong emphasis on employee growth, the company offers numerous opportunities for skill development and career advancement, all while working in a diverse environment that values creativity and teamwork. Located in a vibrant area, employees benefit from a supportive atmosphere that encourages meaningful contributions to patient engagement activities.
