Junior Pharmacovigilance Associate — Patient Safety

Parexel; Olympia (WA); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Health insurance

Vision insurance

Dental insurance

Tuition reimbursement

Vacation time

Flexible Spending Accounts

Work/Life Balance

401(k) with Company match

Pet Insurance

Job summary

Parexel is seeking a Patient Safety Associate I (Pharmacovigilance Associate) to join our pharmacovigilance team. You will contribute to safety operations, case processing, literature review, and regulatory support under supervision.

This role offers remote work in the US, exposure to global drug safety activities, and opportunities to develop expertise in regulatory compliance and clinical research while delivering high-quality patient safety services.

Qualifications

• Bachelor’s degree in Life Sciences or equivalent.
• 3 years experience in Drug Safety; post-marketing experience preferred.
• Experience across multiple therapeutic areas (cardiology, neurology, oncology, rare disease).
• Proficiency with MS Office and ability to learn safety systems/databases.

Responsibilities

• Monitor incoming safety reports and support timely processing.
• Data entry, case processing, quality checks in safety databases.
• Regulatory reporting and submissions tracking support.
• Literature searches and safety information monitoring.
• Support affiliate services and regulatory intelligence activities.
• Maintain documentation in EDMS/eTMF.

Skills

Organizational skills

Attention to detail

Analytical thinking

Pharmacovigilance interest

Team collaboration

Clear communication

Patient focus

Quality & compliance

Pharmacovigilance systems

MS Office

Data workflows

Continuous learning

Education

Bachelor’s degree in Life Sciences

Tools

Veeva Safety

Job description

Parexel is seeking a Patient Safety Associate I (Pharmacovigilance Associate) to join our pharmacovigilance team. You will contribute to safety operations, case processing, literature review, and regulatory support under supervision.

This role offers remote work in the US, exposure to global drug safety activities, and opportunities to develop expertise in regulatory compliance and clinical research while delivering high-quality patient safety services.