At a Glance
- Tasks: Manage Trial Master File activities and ensure compliance in clinical studies.
- Company: Broughton Group, a supportive environment for career growth.
- Benefits: Opportunity for career advancement and skill development.
- Other info: Detail-oriented role with a focus on regulatory standards.
- Why this job: Join a team that makes a real difference in clinical trials.
- Qualifications: 2+ years in clinical trials and strong TMF management skills.
The predicted salary is between 30000 - 40000 £ per year.
Broughton Group is seeking a detail-driven Clinical Trials Associate to support clinical studies by managing Trial Master File (TMF) activities. This role involves ensuring compliance with regulatory standards and contributing to the overall study lifecycle.
The ideal candidate will have at least 2 years of experience in clinical trials, strong TMF management skills, and excellent attention to detail. This is a great opportunity for career growth in a supportive environment.
TMF Specialist: Elevate Clinical Trials Compliance in Hitchin employer: Broughton Group
Broughton Group is an excellent employer that prioritises employee development and fosters a collaborative work culture, making it an ideal place for those passionate about clinical trials. With a focus on compliance and quality, employees benefit from ongoing training opportunities and the chance to contribute meaningfully to impactful research. Located in a vibrant area, the company offers a supportive environment where your skills can flourish and your career can advance.
