Clinical Scientist
US$159,000 – US$205,500 / yr base salary
Posted 16 Sep 2026
Advertised as “Senior Manager, Clinical Scientist”
BranchFactor Summary
The original posting with the fluff stripped out
- Expected experience
- 3+ yrs
- Management level
- Individual contributor
- Employment
- Remote
- Contract
- Full-time
| Base salary | US$159,000 – US$205,500 / yr |
|---|
Study levelBachelor's
CertificationsPharmD, PhD, MD
Overview
Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it.
At Replimune, we live by our values:
United: We Collaborate for a Common Goal.
Audacious: We Are Bold.
Dedicated: We Give Our Full Commitment.
Candid: We Are Honest With Each Other.
People are at the center of everything we do, and when it comes to our employees, we make it personal. With a deep sense of purpose, a strong and evolving culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to impact on the lives of patients, caregivers and themselves.
Join us, as we reshape the future.
Sr. Manager Clinical Scientist, reporting to the (Associate) Director/Sr. Director Clinical Scientist, ensures the successful execution of clinical development programs and deliverables in partnership across the organization, with external vendors, and with external academicians and collaboration partners. The Clinical Scientist works closely in a matrix with the Medical Director and other functional representatives to assure that activities are executed within expected scope, compliance, budget, and timelines. The individual in this position supports the establishment and growth of Clinical Development functions to assure best-in-class global capabilities and execution.
Key responsibilities:
· Facilitate and execute the creation, update, and/or review of key clinical and regulatory documents, including, but not limited to:
o Protocol concepts, synopses, protocols, and amendments
o Informed consent documents
o Investigator Brochures
o Clinical study reports
o Abstracts, posters, and manuscripts
o Clinical sections of INDs (and equivalent applications), Annual Reports, and Developmental Safety Update Reports
o Clinical study supporting documentations and processes, e.g.: charters for (independent) safety data monitoring or steering committee, study specific management plans and manuals, SOPs, etc.
· Supports all clinical and scientific aspects of the design, implementation, conduct, analysis, interpretation and documentation of clinical studies. Partner with relevant functional areas for the successful implementation and execution of clinical studies. Specific tasks will include but are not limited to the following: