Senior Manager, Clinical Scientist, Hematology

Regeneron PharmaceuticalsCambridge, MA
$150,500 - $245,500Hybrid

About The Position

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Clinical Scientist to join our Clinical Sciences team, supporting rare hematologic conditions and/or immunologic diseases. In this role, you will lead the design, execution, and interpretation of clinical studies within a cross-functional matrix environment while collaborating closely with Medical Directors, Clinical Study Teams, and Global Clinical SubTeams to advance early- and late-stage development programs. This position will support rare hematologic conditions and/or immunologic diseases. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

Requirements

  • Bachelor's degree required
  • 8+ years of pharmaceutical clinical drug development experience
  • Demonstrated knowledge of GCP, clinical study design, and clinical research methodology
  • Proven track record driving clinical trial process improvements
  • Strong scientific and analytical skills to complex clinical development challenges

Nice To Haves

  • Advanced degree (PhD/MD/PharmD/MSc) in life sciences or healthcare preferred
  • Experience in rare hematologic conditions and/or immunologic diseases preferred
  • Energized by contributing to therapies for rare and underserved patient populations

Responsibilities

  • Lead clinical study design, execution, and data interpretation across a full development program
  • Partner with Medical Directors and cross-functional teams to shape study strategy and scientific direction
  • Author and review key clinical documents, including protocols, amendments, and clinical study reports
  • Drive medical and safety data review to protect patient safety throughout the trial lifecycle
  • Apply deep therapeutic area knowledge to inform study design and risk mitigation
  • Represent Clinical Sciences in scientific advisory boards, steering committees, and safety monitoring meetings
  • Mentor and guide junior team members as part of a growing Clinical Sciences function
  • Ensure compliance with FDA, EMEA, ICH, and GCP standards across all study activities

Benefits

  • annual bonuses or other incentive plans
  • equity awards
  • pension or retirement benefits
  • 401(k) company match
  • health and wellness programs
  • fitness centers
  • insurance benefits (e.g. medical, dental, vision, life and disability)
  • paid time off
  • family support benefits
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