Principal Medical Scientist (project Lead) - Rwe - Poland, Bulgaria, Romania, Spain, Uk - Sponsor-dedicated

Syneos Health

Remote
Medical monitoring and data review
Project scope and milestone management
Collaboration with multinational teams
Syneos Health is a leading fully integrated biopharmaceutical solutions organization focused on accelerating customer success and improving patient outcomes

Job Summary

  • Syneos Health is a leading fully integrated biopharmaceutical solutions organization focused on accelerating customer success and improving patient outcomes.
  • The Principal Medical Scientist will lead project teams, manage medical data review, and provide scientific oversight while collaborating with multiple functional groups and customers.
  • The company emphasizes career development, a supportive culture, and a commitment to diversity, inclusion, and continuous process improvement.

Matching Summary

Syneos Health is a leading fully integrated biopharmaceutical solutions organization focused on accelerating customer success and improving patient outcomes.

Skills & Requirements

Must-have

  • Medical monitoring and data review
  • Project scope and milestone management
  • Collaboration with multinational teams
  • Clinical research process knowledge
  • Good Clinical Practices (GCP) compliance
  • Scientific oversight and training
  • Vendor management for clinical studies

Nice-to-have

  • Strong communication and leadership skills
  • Experience in epidemiology study design
  • Ability to troubleshoot and resolve issues
  • Supportive and engaged line management culture
  • Diversity and inclusion focused environment

Key Requirements

  • BA/BS in life sciences or health field with 5+ years experience
  • MS/MBA with 3+ years experience or PharmD/PhD with 2 years
  • MD/DO with 1 year experience
  • Industry experience in Clinical Scientist or similar role
  • Experience with multinational studies and teams
  • Knowledge of epidemiology study design and analysis
  • Independent authorship of study protocols
  • Experience managing external vendors
  • Strong knowledge of GCP and clinical research process

Work Rights

Not specified

Tailored Resume

Cover Letter