Job Description
Supports clinical trial safety reporting across therapeutic areas and development programs, ensuring accurate and timely case processing, query management, and protocol compliance. Works closely with cross-functional teams to maintain safety standards, resolve issues, and support the execution of clinical trials from early- to late-stage development.
Education Requirement:
Medical degree
Advanced English proficiency. English level will be confirmed during the process.
Work Experience:
Minimum of 2 years of relevant professional experience in clinical practice and/or the pharmaceutical industry, including drug safety, clinical trials, or drug development, with at least 1 year of clinical experience in a patient care setting.
Qualifications & Skills:
Strong understanding of scientific and medical concepts.
Basic understanding of drug development.
Knowledge of GCP and ICH regulations.
Ability to work as part of a cross-functional team.
Effective decision-making and independent problem-solving skills.
Strong time management and organizational skills.




Strong communication skills with advanced oral and written English.
Advanced computer and database skills.
Ability to work under pressure, with a strong sense of responsibility and accountability.
Required Skills:
Adaptability, Adverse Event Report, Clinical Experience, Data Analysis, Data Integrity, Decision Making, Drug Safety Surveillance, Good Clinical Practice (GCP), Medical Writing, Pharmacovigilance, Regulatory Compliance, Risk Management, Safety Reporting, Strategic Thinking, Training and Development
Preferred Skills:
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📌 Medical Doctor with Clinical Experience Interested in Clinical Trials (Bogotá)
🏢 Msd
📍 Bogotá