ZipRecruiter

Log In

1

Senior Pharmacovigilance Data Entry Jobs (NOW HIRING)

Larimar Therapeutics

As the company's senior pharmacovigilance subject matter expert, the Senior Director will provide ... Partner with Clinical Development, Biostatistics/Statistics, Data Management, Medical, Regulatory ...

New

Senior PsychCare

Data Entry Clerk

Houston, TX · On-site

$15/hr

Senior PsychCare has an immediate need for a Data Entry Clerk The Data Entry Clerk is an Entry-Level position within the Patient Intake Department and is primarily responsible for downloading HIPAA ...

Artech Information System LLC

data entry

Schaumburg, IL

$16.75 - $22.25/hr

Position: Data Entry Clerk TIME :8am - 5 pm .. OT may be required.. LOCATION: Schaumburg, IL ... You will report to a data manager or another senior data team member. Understanding of data ...

Conservice

Data Entry Seniors

Mandan, ND

$16 - $21.25/hr

Data Entry - Senior Department: Capturis Overview The Data Entry Process & Performance Auditor will play a critical role in ensuring operational accuracy and consistency within the Senior Data Entry ...

Conservice

Data Entry Seniors

Logan, UT · On-site

$14.75 - $19.50/hr

Data Entry - Senior Department: Capturis Overview The Data Entry Process & Performance Auditor will play a critical role in ensuring operational accuracy and consistency within the Senior Data Entry ...

next page

Showing results 1-20

All JobsGovernment JobsGovernment Services JobsDrug Safety Associate JobsSenior Pharmacovigilance Data Entry Jobs

Senior Pharmacovigilance Data Entry information

See salary details

$12

$19

$29

How much do senior pharmacovigilance data entry jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for senior pharmacovigilance data entry in the United States is $19.67, according to ZipRecruiter salary data. Most workers in this role earn between $15.38 and $21.63 per hour, depending on experience, location, and employer.

What cities are hiring for Senior Pharmacovigilance Data Entry jobs?

Cities with the most Senior Pharmacovigilance Data Entry job openings:

What are the most commonly searched types of Pharmacovigilance Data Entry jobs?

The most popular types of Pharmacovigilance Data Entry jobs are:

What states have the most Senior Pharmacovigilance Data Entry jobs?

States with the most job openings for Senior Pharmacovigilance Data Entry jobs include:

Senior Pharmacovigilance Data Entry jobs near you
Infographic showing various Senior Pharmacovigilance Data Entry job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $40,919 per year, or $19.7 per hour.

Sr. Pharmacovigilance Clinical Scientist

Dawar Consulting

South San Francisco, CA • On-site

$82.66 - $103.32/hr

Other

Medical, Dental, Vision, Retirement

Posted 3 days ago

New

Job description

Sr. Pharmacovigilance Clinical Scientist

South San Francisco, United States | Posted on 07/23/2026

Our client, a worldleader in biotechnology and gene therapy, is looking for an“Sr.Pharmacovigilance Clinical Scientist” based in South San Francisco, CA (Hybrid).

Job Duration:LongTerm Contract(Possibility Of Extension)

Pay Rate : $65/hr on W2

Company Benefits: Medical, Dental,Vision, Paid Sick leave, 401K

The Sr. PV ClinicalScientist supports US Patient Safety by providing expert clinical review,evaluation, and quality oversight of Individual Case Safety Reports (ICSRs) and adverse event (AE) information. This role ensures case processing,follow-up, labeling assessments, and Health Authority submissions comply withcompany SOPs, PV regulations, and applicable global requirements.

The position worksautonomously as a subject matter expert, supports vendor oversight, drivesquality and process improvements, and may lead projects and train internal andexternal teams.

Key Responsibilities
  • Conductclinical review and quality assessment of AE/ICSR cases processedinternally or by vendors.
  • Evaluatecase validity, seriousness, causality, labeling, and follow-uprequirements.
  • Ensureaccurate and timely case processing in the global safety database.
  • Monitorcase quality, error trends, vendor performance, and potential compliancerisks.
  • SupportPV compliance with FDA, ICH, EMA, GVP, and applicable global regulations.
  • Leadprocess improvements, SOP updates, training initiatives, and quality trendreporting.
  • Supportvendor oversight, audits, inspections, reconciliations, and casetransmission verification.
  • Overseefollow-up activities, correspondence, and data corrections.
  • Supporttechnical and medical product complaint reporting and escalation.
  • Collaboratewith cross-functional teams and serve as a subject matter expert forsafety-related activities.
  • Preparepresentations, executive summaries, and scientific/medical documentation.
Required Qualifications
  • Healthcareprofessional degree such as RN/BSN/MSN, PharmD, RPh/BPharm, NP, MD,or related qualification.
  • 5–7+years of pharmacovigilance experience in a biopharmaceutical environment or equivalentclinical experience with strong knowledge of safety regulations.
  • Strongexperience with ICSR case processing and clinical review.
  • Knowledgeof FDA, ICH, EMA, GVP, and global pharmacovigilance regulations.
  • Experiencewith medical/scientific writing, data entry, and project management.
  • Stronganalytical, communication, organizational, and problem-solving skills.
  • Abilityto work independently, manage complex issues, and collaborate effectivelywith internal teams and external vendors.
#J-18808-Ljbffr

Apply