Scientist, Drug Safety (fixed Term)

Laboratory Animal Management Association

Cundinamarca, Colombia
Hybrid
Intake of reportable safety event information
Review, manage and create safety reports
Ensure clinically complete and accurate cases
The Laboratory Animal Management Association is seeking a Clinical Safety Scientist for a fixed-term position in Cundinamarca, Colombia. This role involves supporting safety reporting in clinical trials across various therapeutic areas, requiring collaboration with cross-functional teams and a background in medicine or drug development

Job Summary

  • The Scientist Level 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.

Matching Summary

Match Score: 85

The Laboratory Animal Management Association is seeking a Clinical Safety Scientist for a fixed-term position in Cundinamarca, Colombia. This role involves supporting safety reporting in clinical trials across various therapeutic areas, requiring collaboration with cross-functional teams and a background in medicine or drug development.

Skills & Requirements

Must-have

  • Intake of reportable safety event information
  • Review, manage and create safety reports
  • Ensure clinically complete and accurate cases
  • Generate safety queries to trial sites
  • Prioritize daily work for timely submission
  • Cross-functional collaboration
  • Protocol-specific activities
  • Communicate with protocol lead and team
  • Escalate protocol or event issues

Nice-to-have

  • Strong sense of responsibility and accountability
  • Independent, strong analytical, and problem-solving skills

Key Requirements

  • M.D. with minimum 1 year of clinical work experience
  • 2 years relevant pharmaceutical, drug development, and/or drug safety experience
  • Basic understanding of scientific and medical concepts
  • Basic understanding of drug development
  • Basic knowledge of GCP and ICH regulations
  • Ability to work as part of a cross-functional team
  • Ability to identify and escalate problems
  • Time management and organizational skills
  • Strong communication skills with advanced oral and written English skills
  • Advanced computer, database skills
  • Able to work under pressure

Work Rights

Not specified

Tailored Resume

Cover Letter