Job Description

Under the direction and oversight of the Associate Vice-President, Head of ICMR, ICMR Senior Director, ICMR Directors/Therapeutic Area Team Leads (TAL), the Medical Safety Review (MSR) Physician will:

As required per SOP, provide in-line medical review of individual case safety reports (ICSRs), LLC (Company) clinical trials and other sources, as required, and will include the following actions:

Determine or confirm the need for expedited reporting to regulatory agencies, ensure the quality coherence, and accuracy of the case narrative, performs a medical assessment of the case in the context of the available safety data and the known safety profile, and provide a company statement and a causality assessment which will be included as part of the Individual Case Report.

Improve the accuracy and completeness of the case report by generating medical queries, as needed, which will be communicated to the corresponding site via the safety database. Ensure compliance with global expedited reporting timelines with timely case assessment Under the direction of the MSR Director (TAL) and/or the Senior Director, perform Analysis of Similar Events (AOSE) when applicable May participate in quality review of ICSRs from other MR Physicians and Associates May lead and/or participate in cross-functional projects as the MSR subject matter expert contributing to continuous process improvement of ICSR assessments Consult with the Clinical Director for the trial and with the Clinical Safety and Risk Management (CSRM) Physician, as needed, for cases requiring additional clinical or safety subject matter expertise May participate in the training of the specified MSR Team May participate in process, quality, innovation, technology and other business-related activities May participate on special projects or rotational assignments within or outside of ICMR as part of their professional development.

The MSR Physician will work closely and collaboratively with colleagues in other departments in the Company, including but not limited to: Clinical Safety Scientists, Clinical Directors in Clinical Research, CSRM Physicians, and CSRM Associates and Scientists, Global and US Pharmacovigilance and Global Pharmacovigilance Case Management. The MSR Physician will be an extended member of the Risk Management Safety Teams (RMST’s) for the products that they support, and other relevant sub-teams.

Education Requirement:

*Degree in Medicine.

Required Skills:

Minimum of 1 year experience in clinical medicine following training, with 3 years of experience preferred; this experience is required in patient care settings

A minimum of 3 years of relevant work experience that may include both clinical medicine practice post training and pharmaceutical industry experience required

Strong understanding of scientific and medical concepts

Excellent writing and communication skills in English required

Effective presentation skills and experience influencing and negotiating required

Computer skill required- use of database and basic MS Office suite applications

Problem-solving, conflict resolution, and critical thinking skills are required

Preferred Experience and Skills:

 Medical specialization

Experience in drug safety, pharmacovigilance and/or risk management is highly desirable

Prior medical review and/or case management experience

Relevant Safety Systems Experience (i.e., Argus, ARIS-G, etc.)

Drug development experience (early or late phase clinical research, regulatory affairs, and/or safety/PV)

Demonstrated leadership skills in managing programs & processes, leading meetings, and influencing peers and direct reports to drive results

Experience working and collaborating with global teams

*Please upload your CV in English.

Current Employees apply HERE

Current Contingent Workers apply HERE

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):

Required Skills:

Adaptability, Adaptability, Audit Process Evaluations, Clinical Judgment, Clinical Medicine, Clinical Research, Clinical Risk Management, Clinical Testing, Communication, Compliance Program Development, Conflict Resolution, Critical Thinking, Data Analysis, Decision Making, Detail-Oriented, Drug Safety Surveillance, Early Clinical Development, Ethical Compliance, Medical Review, Medical Writing, Pharmacovigilance, Post Marketing Surveillance, Program Management, Regulatory Affairs Compliance, Regulatory Communications {+ 3 more}

 Preferred Skills:

Job Posting End Date:

06/25/2025

*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.

Requisition ID:R353914