Remote Senior Scientist: Safety Surveillance & Risk

ClinChoice; Oregon; Hybrid; USD 120,000 - 160,000; Full time

Job summary

ClinChoice is seeking a Pharmacovigilance scientist to manage core safety deliverables, lead aggregate analyses, and coordinate strategic safety documents. The role partners with MSOs and SMT, supervising ad hoc product safety tasks and ensuring PVAs and assessments are met.

The candidate will oversee data searches, safety reviews, and cross-functional collaboration across multiple therapeutic areas, with a focus on high-quality safety reporting and compliance.

Qualifications

• Strong English verbal and written communication skills.
• Experience in pharmacovigilance or clinical research is preferred.
• Knowledge of drug development and global safety regulations is highly preferred.

Responsibilities

• Ensure timely safety deliverables and aggregate reports.
• Collaborate with TASH, MSO, SSP and stakeholders on strategy.
• Initiate and oversee database searches for safety analyses.
• Perform aggregate safety analysis and case-level review.
• Coordinate core safety deliverables and maintain PVAs and reports.
• Lead cross-functional safety initiatives and SMT support.

Skills

Strong English communication

Education

Bachelor’s degree in Health or Biomedical Science with 6–8 years experience

Advanced degree in Health or Biomedical Science with 4–6 years experience

Job description

ClinChoice is seeking a Pharmacovigilance scientist to manage core safety deliverables, lead aggregate analyses, and coordinate strategic safety documents. The role partners with MSOs and SMT, supervising ad hoc product safety tasks and ensuring PVAs and assessments are met.

The candidate will oversee data searches, safety reviews, and cross-functional collaboration across multiple therapeutic areas, with a focus on high-quality safety reporting and compliance.