Medical Advisor, Colombia

CSL Behring

Bogota, Colombia
**
University degree in medicine md
Minimum 5 years medical advisor experience
Fluent in english and spanish
** CSL Behring is seeking a Medical Advisor in Bogota, Colombia, to act as a key scientific liaison for the company, providing medical expertise and support for various activities related to its products. The role involves collaboration with internal teams and external stakeholders, requiring strong communication skills and a solid background in the pharmaceutical or biotech industry. **

Job Summary

  • This role serves as the main CSL interface for internal and external partners regarding scientific medical knowledge and expertise on CSL/Vifor products.
  • The successful candidate will drive locally initiated clinical activities and coordinate the publication of local clinical research outcomes.
  • CSL Behring is a global biotherapeutics leader driven by a promise to save lives through innovative therapies in immunology, hematology, and other therapeutic areas.

Matching Summary

Match Score: 75

** CSL Behring is seeking a Medical Advisor in Bogota, Colombia, to act as a key scientific liaison for the company, providing medical expertise and support for various activities related to its products. The role involves collaboration with internal teams and external stakeholders, requiring strong communication skills and a solid background in the pharmaceutical or biotech industry. **

Skills & Requirements

Must-have

  • University Degree in Medicine MD
  • Minimum 5 years Medical Advisor experience
  • Fluent in English and Spanish
  • Experience with clinical trials
  • Knowledge of Colombian pharmaceutical legislation

Nice-to-have

  • Masters or PhD degree preferred
  • Relationships with scientific societies and KOLs
  • Action and results oriented mindset
  • Political savvy in complex situations
  • Experience with reimbursement processes

Key Requirements

  • MD degree required
  • 5+ years experience in high tech/biotech pharma
  • Demonstrated relationships with regulatory authorities
  • General clinical trial experience required

Work Rights

Not specified

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