# Clinical Safety and Risk Management Associate Principal Scientist

Hiring organization: [Merck](https://career.thegoodapps.co/organizations/merck)

Canonical page: https://career.thegoodapps.co/jobs/8370bf2e-704b-40d9-a5c9-e6f1d8c42483

Listed on Merck's own careers site. Applications go to them directly.

- Employment type: full time
- Seniority: Principal

## Summary

A medical specialist responsible for reviewing adverse event reports and developing safety strategies for pharmaceutical products in collaboration with physicians and cross-functional teams. This role suits someone with clinical background and drug safety expertise who can manage complex regulatory and pharmacovigilance responsibilities.

_Our summary, not Merck's wording._

## Skills named

Critical Thinking, Data Analysis, Database Management, Epidemiology, Medical Writing, Pharmacovigilance, Risk Management

## Required

- Medical Doctor (MD) degree
- At least 2 years clinical experience in patient care setting
- Minimum 5 years professional experience with both clinical and pharmaceutical industry background
- Minimum 2 years safety experience including causality assessment, aggregate safety data analysis, or safety document authoring
- Experience in drug safety, pharmacovigilance, or risk management
- Excellent English writing and communication skills
- Demonstrated leadership in managing programs and facilitating meetings
- Effective presentation and negotiation skills
- Computer skills including database and MS Office applications
- Problem solving, conflict resolution, and critical thinking ability

## Nice to have

- Subject matter expertise in departmental programs, SOPs, and initiatives

Apply on Merck's site: https://msd.wd5.myworkdayjobs.com/en-US/SearchJobs/job/CZE---Central-Bohemian---Prague-Five/Clinical-Safety-and-Risk-Management-Associate-Principal-Scientist_R405854-1