Bristol Myers Squibb

Biopharma

Manager,PatientSafety,EpidemiologyScienceandExecution

$154–187k Poland FULL TIME Remote Friendly
The Brief

“Manager, Patient Safety, Epidemiology Science and Execution at Bristol Myers Squibb. Skills: Epidemiology study execution, Regulatory document drafting, Cross-functional coordination, Risk identification and escalation, Continuous improvement initiatives. Executing assigned epidemiology study components. Conducting literature reviews”

What You'll Achieve.

Ensure BMS medicines are as safe as they are transformative; Feed directly into benefit-risk decisions; Contribute to regulatory-grade science; Produce inspection-ready documentation; Assess adverse events; Study disease natural history; Evaluate background rates; Contextualize safety signals

Industry & Context.

Biopharma
Problems you'll solve

Spot problems before they become problems; Identifying execution-level risks and escalating with proposed solutions

Eligibility Requirements

Approximately 5% travel involved for key scientific congresses, regulatory meetings, and engagements

What They're Looking For.

Must Have

scientific or biomedical degree (BS, MPH, PharmD, RN, MD, PhD or equivalent), at least 2 years of relevant experience, Reads the details others miss, Juggles multiple priorities without dropping the scientific thread, Communicates clearly, Thrives in a structured environment while still bringing your own thinking to the table

Nice to Have

Curious about how AI tools are shaping modern scientific work

What You'll Do.

Executing assigned epidemiology study components

Conducting literature reviews

Assessing data sources

Contributing to study protocols

Contributing to analysis plans

Contributing to regulatory documents

Drafting sections of safety study protocols

Drafting study reports

Drafting risk management plans

Drafting aggregate safety reports

Coordinating with cross-functional teams

Navigating dependencies

Identifying execution-level risks

Escalating risks with proposed solutions

Contributing to continuous improvement initiatives

How You'll Work.

Team & Collaboration

Work within a collaborative, senior-led epidemiology team; Coordinate with cross-functional teams; Collaborate across drug development and lifecycle management

Communication Scope

Communicates clearly — whether you're writing a regulatory document or explaining a finding to a cross-functional colleague

Process & Methodology

Manage timelines, Navigate dependencies, Coordinate cross-functional activities

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