At a Glance
- Tasks: Lead study start-up activities and manage submissions for clinical trials.
- Company: Join a leading organisation in the clinical research field.
- Benefits: Competitive salary, professional development, and a dynamic work environment.
- Other info: Opportunity to work with experts and grow your career in clinical research.
- Why this job: Be at the forefront of clinical innovation and make a real difference.
- Qualifications: Degree in a scientific field and experience in Clinical Operations required.
The predicted salary is between 60000 - 80000 £ per year.
Responsibilities
- Lead end-to-end study start-up activities
- Manage Ethics Committee (EC) and Competent Authority (CA) submissions
- Provide robust CRO oversight
- Act as the primary contact and clinical trial expert
- Develop critical study documentation
Requirements
- A degree in a scientific discipline or related field
- Direct experience in Clinical Operations
- Demonstrated experience in CRO oversight
- Strong understanding of In Vitro Diagnostic Regulation (IVDR)
- Exceptional verbal and written communication skills (English)
We think you need these skills to ace Lead Clinical Site Manager – Study Start Up, In Vitro Diagnostic Regulation in Burgess Hill
End-to-End Study Start-Up
Ethics Committee (EC) Submissions
Competent Authority (CA) Submissions
CRO Oversight
Clinical Trial Expertise
Study Documentation Development
Clinical Operations Experience
