MSD

Medical Safety Review Physician, Associate Principal Scientist

MSD  •  Warsaw, PL (Hybrid)  •  16 days ago
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Job Description

As an Individual Case Medical Review (ICMR) Physician, you apply your clinical expertise to ensure patient safety and high‑quality medical assessments. You work in close collaboration with global medical and safety experts, contributing to informed safety and risk‑management decisions.

What you will do

Under the guidance of experienced medical leaders, you review and medically assess individual patient safety cases from a wide range of sources.

Your main responsibilities include:

  • Performing medical review of individual safety cases in line with established procedures

  • Assessing cases based on available safety data and known product safety profiles

  • Determining whether cases require expedited reporting to health authorities

  • Ensuring accurate, high‑quality case documentation, including medical assessments and causality evaluations

  • Supporting timely reporting by meeting global safety timelines

  • Collaborating with clinical safety and risk management colleagues on complex cases

  • Contributing to quality reviews, training activities, cross‑functional projects, and process improvements within the team

What skills you will need

To be successful in this role, you bring the following qualifications and skills:

  • Medical Doctor or equivalent non‑US degree in Medicine

  • At least one year of post‑training clinical experience with direct patient care (three years preferred)

  • A minimum of three years of relevant professional experience post‑training, which may include clinical practice and/or pharmaceutical industry experience

  • Strong understanding of medical and scientific concepts

  • Excellent written and verbal communication skills in English

  • Effective presentation skills and experience influencing and collaborating with stakeholders

  • Solid computer skills, including use of databases and standard office applications

  • Strong analytical thinking, problem‑solving ability, and sound clinical judgment

Preferred experience and skills

Ideally, you bring some of the following experience:

  • Medical specialization or prior experience in drug safety, pharmacovigilance, or risk management

  • Experience with medical case review, case management, or related safety activities

  • Familiarity with drug development processes and/or regulatory or safety environments

  • Experience working with safety databases or related systems (e.g. Argus, ARIS‑G)

  • Experience collaborating in international, cross‑functional teams

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment.

Required Skills:

Accountability, Accountability, Adaptability, Audit Process Evaluations, Business Administration, Case Writing, Clinical Judgment, Clinical Medicine, Clinical Research, Clinical Risk Management, Clinical Sciences, Clinical Trials, Compliance Program Development, Continuous Process Improvement, Critical Thinking, Data Analysis, Decision Making, Detail-Oriented, Drug Safety Surveillance, Ethical Compliance, Healthcare Risk Management, Innovation, Machine Learning (ML), Medical Writing, Pharmacovigilance {+ 4 more}

Preferred Skills:

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Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

04/5/2026

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

MSD

About MSD

At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.

Industry
Chemicals & Materials
Company Size
10,000+ employees
Headquarters
Rahway, New Jersey
Year Founded
Unknown
Website
msd.com
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