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Scientist, Drug Safety

MSD


Job Location:

Bogotá - Colombia

Monthly Salary: Not provided by the employer
Posted: 28 May 2026 (30+ days ago)
Application Deadline: 25 August 2026
Vacancies: 1 Vacancy
The job posting is outdated and position may be filled

Job Summary

Job Description

The Clinical Safety Scientist (CSS) is responsible for support of safety reporting in clinical trials conducted in multiple therapeutic areas as part of investigational product development programs across early and late-stage development. Assists the protocol lead in safety reporting activities for multiple clinical trials. The CSS may support collaboration with cross-functional colleagues within clinical development clinical operations case processing and medical safety review.

Key Responsibilities:

Intake of reportable safety event information from clinical trial investigator sites.

Review and manage individual case safety reports for each event.

Ensure that all information required for a clinically complete and accurate case is present.

Generate safety queries to the trial investigator sites to ensure case report accuracy and

completeness.

Prioritize daily work to ensure all events are submitted for entry into the safety database

within the established timeframes.

May collaborate with cross-functional colleagues as needed.

Complete protocol specific activities as required

Actively participate and ensure effective communication with protocol lead and other team

members supporting their protocols

Appropriately escalate protocol or individual event issues with other stakeholders including

CRAs/CRMs

Required Skills:

Adaptability Adaptability Adverse Event Report CiviCRM Clinical Development Clinical Medicine Clinical Physiology Clinical Reporting Clinical Risk Management Clinical Sciences Clinical Trial Management Clinical Trials Monitoring Cross-Functional Collaboration Data Integrity Data Management Detail-Oriented Drug Safety Surveillance Good Clinical Practice (GCP) Medical Device Management Pharmacokinetics Product Development Protocol Development Regulatory Communications Regulatory Compliance Audits Regulatory Interpretation 2 more

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

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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:

Project Temps (Fixed Term)

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

05/28/2026

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


Required Experience:

IC


About Company

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Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more

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