Medical Affairs Operations Leader

Roche

Basel, Switzerland
Not specified; details provided based on primary p...
Fully remote
5 years pharmaceutical industry experience
Non-interventional study operational leadership
Gcp, gpp, iso, eu-gvp regulatory compliance
Roche is seeking a Medical Affairs Operations Leader to manage non-interventional studies, providing operational leadership and ensuring compliance with global regulatory standards. The ideal candidate will have over five years of relevant experience in the pharmaceutical industry, with strong project management skills and a focus on collaboration and stakeholder engagement

Job Summary

  • This role drives impactful real-world evidence generation by designing and coordinating non-interventional studies within a culture that values personal expression and genuine connections.
  • The successful candidate will ensure global regulatory compliance and inspection readiness across the study lifecycle while managing complex relationships with CROs, vendors, and affiliates.
  • Roche offers an environment where over 100,000 employees collaborate to advance science and deliver life-changing healthcare solutions globally.

Matching Summary

Match Score: 85

Roche is seeking a Medical Affairs Operations Leader to manage non-interventional studies, providing operational leadership and ensuring compliance with global regulatory standards. The ideal candidate will have over five years of relevant experience in the pharmaceutical industry, with strong project management skills and a focus on collaboration and stakeholder engagement.

Salary

Not specified; details provided based on primary posting location later in hiring process

Skills & Requirements

Must-have

  • 5 years pharmaceutical industry experience
  • Non-interventional study operational leadership
  • GCP, GPP, ISO, EU-GVP regulatory compliance
  • CRO and vendor management expertise
  • Budget forecasting and milestone tracking

Nice-to-have

  • Cross-functional multicultural collaboration
  • Strong stakeholder negotiation skills
  • Data analysis and clinical platform proficiency
  • Coaching and team development capabilities
  • Process optimization and documentation skills

Key Requirements

  • Minimum 5 years in pharmaceutical or CRO setting
  • Hands-on experience in clinical or real-world evidence studies
  • Expertise in drug and device development regulations
  • Proven ability to manage multiple studies simultaneously

Work Rights

Not specified

Tailored Resume

Cover Letter