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Aequor Technologies LLC

Sr. Pharmacovigilance (PV) Clinical Scientist

Pay: Not specified

Posted: 6 weeks ago

Location: South San Francisco, CA (Hybrid)

Last Updated: 3 weeks ago

Hours: Full-Time

Expires: 9/10/2026

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What they do

A Clinical Data Specialist manages data and information gathered during a clinical trial, including studies of medical treatments and drugs.

$88,154 / year median in California

+2% projected growth

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Job Description

Sr. Pharmacovigilance (PV) Clinical Scientist Aequor Technologies

LLC - 4.0

South San Francisco, CA Job Details Contract 11 hours ago Qualifications Medical writing Pharmaceutical regulatory compliance Safety regulations Drug regulation ICH guidelines Data entry Managing projects FDA regulations

Full 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])

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) #TechRV