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1 hour ago
Type
Full time
Salary
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Related skills

regulatory affairs clinical research medical writing oncology study design

πŸ“‹ Description

  • Collaborate with Medical, Strategy, and BD leaders to support client engagements.
  • Support BD/Proposals in RFPs; draft medical sections and assist bid defenses.
  • Write or edit scientific content within budgets and timelines.
  • Collaborate with Regulatory Affairs on product landscape and strategy.
  • Provide scientific insights for company releases (white papers, manuscripts).
  • Review protocols, CRFs, training materials, and study designs.

🎯 Requirements

  • MD, DO, MBBS or equivalent.
  • 5+ years of clinical experience.
  • Completed an accredited medical residency program.
  • Completed oncology/hematology fellowship or equivalent.
  • 5+ years in oncology or autoimmune disease clinical research.
  • Availability for domestic and international travel (~30%).

🎁 Benefits

  • Discretionary annual bonus
  • Health insurance
  • Retirement savings benefits
  • Life insurance
  • Disability benefits
  • Parental leave
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