Ctma Associate Line Manager

BeiGene

France
Base: 61,700.00 eur - 77,100.00 eur; bonus/equity:...
**
50/50 line management and operations balance
Ich/gcp and local regulation adherence
Clinical trial document and tmf management
** BeiGene is seeking a Ctma Associate Line Manager in France, who will be responsible for line management and operational duties within clinical research. The ideal candidate should have a background in oncology, strong organizational skills, and experience in managing clinical trial teams. **

Job Summary

  • The role combines line management of up to 10 direct reports with operational responsibilities in a 50/50 split to support the fight against cancer.
  • Candidates must demonstrate mastery of clinical operations tasks including maintaining the Trial Master File and adhering to ICH/GCP standards.
  • BeOne seeks highly motivated professionals who share a passionate interest in fighting cancer and can drive operating excellence through continuous learning.

Matching Summary

Match Score: 75

** BeiGene is seeking a Ctma Associate Line Manager in France, who will be responsible for line management and operational duties within clinical research. The ideal candidate should have a background in oncology, strong organizational skills, and experience in managing clinical trial teams. **

Salary

Base: 61,700.00 EUR - 77,100.00 EUR; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • 50/50 line management and operations balance
  • ICH/GCP and local regulation adherence
  • Clinical trial document and TMF management
  • Staff performance review and development
  • CTMS EDC and IRT tool proficiency

Nice-to-have

  • Oncology industry experience preferred
  • Advanced scientific degree preferred
  • Collaborative spirit and innovation mindset
  • Leadership in global workstreams
  • Strategic contribution to clinical operations

Key Requirements

  • Bachelor's degree in scientific or healthcare discipline
  • Minimum 3 years pharmaceutical or CRO industry experience
  • Prior clinical trial management or leadership experience
  • Expert knowledge of drug development process and ICH-GCP

Work Rights

Not specified

Tailored Resume

Cover Letter