Clinical Safety Scientist (Temporary)

About the role

We are looking for a Clinical Safety Scientist to support safety reporting across multiple therapeutic area clinical trials. The role is temporary and will work closely with protocol leads and cross‑functional teams to ensure accurate and timely case safety reporting.

Key responsibilities

• Intake and review reportable safety event information from investigator sites.
• Manage individual case safety reports and ensure completeness and clinical accuracy.
• Generate and follow up on safety queries to investigators.
• Prioritize daily workload to meet database entry timelines.
• Collaborate with clinical development, operations, case processing and medical safety review teams.
• Escalate protocol or event issues to CRAs, CRMs or protocol leads as needed.

Required profile

• MD/DO, PharmD, MS, BSN, NP or RN with a minimum of 1 year experience in patient care, drug safety or pharmaceutical development.
• Basic understanding of scientific, medical and drug development concepts.
• Knowledge of GCP and ICH regulations.
• Strong analytical, problem‑solving and time‑management abilities.

Required skills

• Advanced computer and database skills.