Senior Manager, Clinical Scientist

Replimune

. Ensure successful execution of clinical development programs and deliverables in partnership across the organization, with external vendors, academicians, and collaboration partners .

Posted 9/16/2026full-timeRemote • Massachusetts • United StatesSenior💰 $159,000 - $205,500 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical development, particularly in oncology, with a strong focus on regulatory compliance, project management, and collaboration across diverse teams. Proficient in creating and reviewing clinical documents while providing scientific support throughout clinical trials.

Highest-signal resume keywords

Clinical Development ExpertiseOncology Therapeutic Area KnowledgeGCP and ICH Guidelines KnowledgeClinical Trial Data AnalysisProject Management Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial DesignRegulatory Document CreationClinical Study ImplementationData AnalysisRisk MitigationClinical Oncology ExperienceClinical Development Program ParticipationTherapeutic Area ResearchKOL EngagementClinical Protocol Training

Soft Skills

Problem SolvingTime ManagementOrganizational SkillsRelationship BuildingFlexibility

Tools & Technologies

Clinical Development IT SolutionsMicrosoft WordMicrosoft PowerPointMicrosoft Excel

Certifications & Qualifications

Bachelor's DegreeAdvanced Degree (PharmD, PhD, MD Preferred)

Industry Keywords

BiotechPharmaceuticalClinical TrialsGCPICH GuidelinesEarly/Late Phase DevelopmentInvestigator BrochuresInformed ConsentsIND Clinical SectionsSafety Update Reports

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Ensure successful execution of clinical development programs and deliverables in partnership across the organization, with external vendors, academicians, and collaboration partners
Work in a matrix with the Medical Director and functional representatives to execute activities within scope, compliance, budget, and timelines
Support establishment and growth of Clinical Development functions and global capabilities
Facilitate and execute creation, updating, and review of clinical and regulatory documents, including protocols, informed consents, Investigator Brochures, clinical study reports, publications, IND clinical sections, annual reports, safety update reports, charters, management plans, manuals, and SOPs
Support clinical and scientific aspects of clinical study design, implementation, conduct, analysis, interpretation, and documentation
Provide clinical and scientific expertise for investigator/site staff and vendor selection
Train internal colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or clinical protocol
Provide scientific and medical support throughout clinical trials and respond to questions from sites, IRBs/IECs, Health Authorities, and CROs
Review, query, and analyze clinical trial data
Partner with the Medical Director on medical monitoring, patient eligibility, and study treatment-related questions
Present clinical trial data internally and externally
Create clinical study and program-related slide decks
Represent clinical studies or development programs on teams or sub-teams
Build and maintain KOL/investigator networks; organize and present at KOL advisory boards and investigator meetings; engage advocacy groups
Conduct or contribute to therapeutic area/indication research and competitor analysis
Build relationships with internal experts
Develop, track, execute, and report on goals and objectives
Ensure compliant business practices

Requirements

What you’ll need

Minimum of a Bachelor's degree required
Minimum of 3+ years of experience and success within the function in other biotech / pharmaceutical companies
1-2 years in the oncology therapeutic area
Previous participation in an Early/Late clinical development program is essential
Clinical oncology experience required for Late Phase; preferred for Early Phase
Knowledge of GCP and ICH Guidelines
Flexibility to work with colleagues in a global setting
Ability to travel approximately 25% for work
Knowledge of industry standard Clinical Development IT solutions
Problem solving and risk-mitigation skills
Ability to work independently and build working relations throughout the organization and with business partners
Strong time management and organizational skills
Ability to manage multiple projects in a fast-paced environment
Skilled in computer-based tools including Word, PowerPoint, and Excel
Advanced degree such as PharmD, PhD, or MD preferred

Benefits

Comp & perks

Annual performance incentive bonus
New hire equity
Ongoing performance-based equity
Medical insurance
Dental insurance
Vision insurance
401k match
Flexible time off
Paid holidays, including year-end shutdown