Medical Safety Reviewer

hace 3 días

Bogotá, Colombia MSD A tiempo completo

The Medical Safety Review (MSR) Physician will:
1. Provide in-line medical review of individual case safety reports, 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.

2. 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.

3. Ensure compliance with global expedited reporting timelines with timely case assessment.

4. Under the direction of the MSR Director, perform Analysis of Similar Events (AOSE) when applicable

5. May participate in quality review of ICSRs (Individual Case Safety Reports) from other MR Physicians and Associates

8. May participate in the training of the specified MSR Team

9. May participate in process, quality, innovation, technology and other business-related activities

10. 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**:
M.D./D.O. or equivalent degree in Medicine
- Minimum of 1 year experience in clinical medicine, with 3 years of experience preferred. This experience is required in patient care setting.
- Minimum of 3 years: clinical practice experience, following training or prior industry experience in safety, clinical development and/or medical affairs
- Strong understanding of scientific and medical concepts
- Excellent writing and communication skills in English required
- Effective presentation skills and experience in influencing and negotiating required
- Computer skill required
- Problem-solving, conflict resolution, and critical thinking skills are required

**Preferred Experience and Skills**:

- Board certification
- 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

**Search Firm Representatives Please Read Carefully**

**Employee Status**:
Regular

**Relocation**:
**VISA Sponsorship**:
**Travel Requirements**:
**Flexible Work Arrangements**:
Not Applicable

**Shift**:
**Valid Driving License**:
**Hazardous Material(s)**:
**Job Posting End Date**:
03/14/2025

**Requisition ID**:R338512

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