Sr. Pharmacovigilance (PV) Clinical Scientist

Aequor; South San Francisco (CA); Hybrid; USD 90,000 - 130,000; Full time

Job summary

Aequor is seeking a Sr. Pharmacovigilance Clinical Scientist to lead PV activities in a hybrid work setting at South San Francisco, CA. This contract role focuses on safety signal management, data review, and regulatory compliance.

You will collaborate with medical writing teams, coordinate case processing, and support FDA/ICH/EMA requirements, with a typical schedule Monday–Friday, 8:00–4:30 PT.

Qualifications

• Health care professional degree required (RN/BSN/MSN/NP/RPh/PharmD/MD).
• 5–7 years experience in a biopharma company with pharmacovigilance responsibilities or equivalent clinical experience with FDA/ICH/EMA knowledge.
• Writing experience; science/medical writing required.
• Computer proficiency and data entry experience.
• Project management experience required.

Skills

PV experience

Medical writing

Regulatory knowledge

Project management

Data entry / Computer skills

Education

Health Care Professional degree

Job description

Job Title: Sr. Pharmacovigilance (PV) Clinical Scientist

Working Model: Hybrid, South San Francsico, CA 94080

Duration: 6+ months contract

Working Days: Monday through Friday

Working Hours: 8 AM to 4:30 PM PT

Interview Format: Two Rounds (1. Hiring Manager [30 minutes]; 2. Upper Management [30 minutes])

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Education, Experience, and Other Requirements:

• Health Care Professional degree (e.g., RN/BSN/MSN, NP, RPh/B Pharm/Pharm D, or MD) (Required)
• Minimum 5 - 7 years of experience in a biopharma company with Pharmacovigilance responsibilities (Preferred); OR equivalent clinical experience with thorough understanding of FDA safety regulations, ICH guidelines, and other applicable regulatory guidance documents, global PV regulatory environment, EMA regulations (Required)
• Writing experience; science/medical writing (Required)
• Computer proficiency and Data entry experience (Required)
• Project Management (Required)