Senior Clinical Scientist – Oncology Development

Replimune-2

Woburn (MA)

On-site

USD 159,000 - 206,000

Full time

12 days ago
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Benefits offered by this job

Medical, Dental, Vision Insurance
401k Match
Flexible Time Off
Paid Holidays

Job summary

Replimune Group, Inc. in Woburn, MA seeks a Sr. Manager Clinical Scientist to lead clinical development programs, coordinating with Medical Directors, CROs, and external partners to ensure timelines, scope, and compliance. The role supports building global capabilities within the Clinical Development function.

You will review clinical and regulatory documents, contribute to study design, and present data to internal and external stakeholders. Travel ~25% is expected.

Qualifications

  • Minimum of 3+ years in biotech/pharma with oncology experience.
  • Experience in Early/Late clinical development programs essential.
  • Strong communication and cross-functional collaboration skills.
  • Knowledge of GCP and ICH Guidelines.
  • Willingness to travel ~25%.
  • Advanced degree preferred (PharmD/PhD/MD).

Responsibilities

  • Create and review clinical and regulatory documents.
  • Coordinate with vendors, sites, and CROs.
  • Present trial data internally and externally.
  • Train staff on therapeutic area and protocol.
  • Support medical monitoring and patient eligibility questions.
  • Build KOL networks and engage investigators.

Skills

GCP & ICH Guidelines
Clinical Development
Regulatory Documentation
Cross-functional Collaboration
Medical Monitoring

Education

Bachelor's degree
Advanced degree preferred (PharmD/PhD/MD)

Tools

Clinical Development IT solutions
SOPs & policies development

Job description

Replimune Group, Inc. in Woburn, MA seeks a Sr. Manager Clinical Scientist to lead clinical development programs, coordinating with Medical Directors, CROs, and external partners to ensure timelines, scope, and compliance. The role supports building global capabilities within the Clinical Development function.

You will review clinical and regulatory documents, contribute to study design, and present data to internal and external stakeholders. Travel ~25% is expected.

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