Clinical Safety Scientist Job at MSD, Columbia
Interested in building a career in drug safety and clinical research? This Clinical Safety Scientist role offers an excellent opportunity to work on safety reporting across multiple clinical trials. You will contribute to investigational product development in both early and late-stage programs. The candidate selected for the Clinical Safety Scientist Job at MSD Careers involves collaboration with cross-functional teams in clinical development and safety. This Job in Colombia is ideal for medical professionals looking to grow in pharmacovigilance and drug safety domains.
About the Company:
Merck & Co., Inc., also known as Merck Sharp & Dohme, is a global healthcare company dedicated to delivering innovative health solutions through medicines, vaccines, and biologic therapies. With a strong focus on research and development, the company works across multiple therapeutic areas to improve patient outcomes worldwide.
Job Details
- Job Role: Scientist, Drug Safety (Clinical Safety Scientist)
- Requisition ID: R393847
- Location: Bogotá, Cundinamarca, Colombia
- Job Type: Fixed Term (Project Temps)
- Work Mode: Hybrid
- Application Deadline: April 24, 2026
- Company: Merck & Co., Inc.
Key Responsibilities:
- Manage the intake of safety event information from clinical trial sites
- Review and create individual case safety reports
- Ensure completeness and accuracy of clinical safety data
- Generate safety queries to investigators for clarification in this Clinical Safety Scientist Job at MSD Careers
- Maintain timelines for safety data entry and reporting
- Collaborate with cross-functional teams in clinical development
- Support protocol-specific safety activities in this Job in Colombia
- Communicate effectively with protocol leads and team members
- Escalate safety issues and contribute to resolution
Educational Requirements for this Job:
- M.D. / D.O. or equivalent medical degree
- Minimum 1 year of clinical experience or
- 2 years of experience in pharmaceutical, drug development, or drug safety
Skills Required:
- Basic understanding of clinical medicine and drug development
- Knowledge of GCP and ICH regulations
- Strong analytical and problem-solving skills
- Excellent written and verbal communication skills
- Ability to work in cross-functional teams
- Strong organizational and time management skills
- Proficiency in computer and database systems
- Attention to detail and data integrity
Benefits of the Clinical Safety Scientist Job:
- Opportunity to work in global clinical trials and drug development
- Exposure to pharmacovigilance and safety reporting processes
- Hybrid work flexibility
- Experience across multiple therapeutic areas
- Career growth in clinical safety and regulatory domains
- Work with a globally recognized healthcare organization.
