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Merck Pharmacovigilance Jobs (NOW HIRING)

Merck & Co.

Shape the QB pharmacology portfolio and resourcing strategy, contributing to early target and end ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

Merck & Co.

Shape the QB pharmacology portfolio and resourcing strategy, contributing to early target and end ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

Merck & Co.

The Pharmacokinetics, Dynamics, Metabolism and Bioanalytics (PDMB) group is seeking a dynamic ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

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Merck & Co.

The Safety & Exploratory Pharmacology (SEP) collaborates with our discovery research, preclinical ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

Merck & Co.

We are seeking an experienced talented scientist to join the - Quantitative Pharmacology and ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

Merck & Co.

$95K - $121K/yr

Ph.D. in Pharmaceutical Sciences, Analytical Chemistry, Biochemistry, Pharmacology, or a related ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

Merck & Co.

The Pharmacokinetics, Dynamics, Metabolism and Bioanalytics (PDMB) group is seeking a dynamic ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

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How much do merck pharmacovigilance jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for merck pharmacovigilance in the United States is $61.42, according to ZipRecruiter salary data. Most workers in this role earn between $42.55 and $73.80 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Merck Pharmacovigilance?

To excel in Merck Pharmacovigilance, candidates typically need a background in life sciences or pharmacy, strong knowledge of drug safety regulations, and experience in adverse event reporting and clinical data analysis. Familiarity with pharmacovigilance software (such as Argus Safety), global regulatory requirements, and GVP (Good Pharmacovigilance Practice) certification is highly valued. Attention to detail, effective communication, and critical thinking are important soft skills for successfully collaborating with cross-functional teams and ensuring regulatory compliance. These skills ensure accurate monitoring, timely reporting, and mitigation of drug-related risks, directly impacting patient safety and regulatory success.

What is a Merck Pharmacovigilance?

A Merck Pharmacovigilance job involves monitoring, assessing, and preventing adverse effects of pharmaceutical products to ensure patient safety and regulatory compliance. Professionals in this role collect and analyze drug safety data, report adverse events to health authorities, and implement risk management strategies. They collaborate with cross-functional teams, including regulatory affairs and clinical development, to maintain drug safety standards. Strong analytical skills, attention to detail, and knowledge of global regulatory requirements are essential for success in this field.

What does a Merck Pharmacovigilance do?

A typical day in Merck Pharmacovigilance involves reviewing and assessing reports of adverse drug events, ensuring proper documentation within safety databases, and preparing regulatory submissions. Team members frequently collaborate with clinical, regulatory, and medical affairs colleagues to analyze safety data, respond to queries, and monitor trends that could impact product safety. The work environment is fast-paced and detail-oriented, with a strong emphasis on accuracy, timelines, and compliance with international guidelines. Over time, professionals in this role gain opportunities to lead projects, mentor new team members, and advance into specialist or managerial positions within the organization.

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Merck Pharmacovigilance jobs near you
Infographic showing various Merck Pharmacovigilance job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 60% In-person, 20% Hybrid, and 20% Remote job distribution, with an average salary of $127,745 per year, or $61.4 per hour.

Pharmacovigilance Specialist / Assistant

Kaav Inc.

Boston, MA • On-site

Other

Posted 5 days ago

Job description

Job Title: Pharmacovigilance Specialist / Assistant
Location: Remote (Candidates in Fort Worth, TX or Boston, MA preferred for future hybrid)
Job Summary:
seeking a Pharmacovigilance Specialist to support adverse event case processing and safety reporting. This role is highly interactive and requires working closely with patients, healthcare professionals (HCPs), vendors, and internal teams.
The ideal candidate will have strong experience in drug safety, case processing, and regulatory compliance (FDA/Health Canada), along with the ability to operate in a fast-paced, high-volume environment.
Key Responsibilities:
Adverse Event Case Management (50%)
  • Review and evaluate incoming communications (phone, email, fax, etc.) for adverse event (AE) reporting
  • Perform medical evaluation of AE cases for seriousness and reporting requirements
  • Process and manage cases in safety databases (e.g., ARGUS)
  • Conduct follow-ups to gather missing or additional case information
  • Prepare and submit expedited and periodic safety reports to FDA and Health Canada
  • Ensure AE intake from marketing programs and social media platforms
  • Support audits and regulatory inspections
  • Perform trend analysis and signal detection reporting
Regulatory & Product Knowledge (25%)
  • Maintain knowledge of FDA & Health Canada pharmacovigilance regulations
  • Understand company SOPs, drug safety processes, and compliance requirements
  • Develop knowledge of Galderma products and dermatology-related conditions
Data & Case Tracking (15%)
  • Maintain and update case tracking systems and databases
  • Perform reconciliation with Medical Information, Quality, and external partners
Training & Support (10%)
  • Develop and deliver training on adverse event reporting
  • Support onboarding of new employees and vendors
  • Assist in SOP creation and process documentation
Required Qualifications:
  • Bachelor's degree in Life Sciences, Healthcare, or related field
  • 5+ years of Pharmacovigilance / Drug Safety experience
  • Strong experience in case processing and adverse event reporting
  • Knowledge of FDA and Health Canada safety regulations
  • Hands-on experience with ARGUS or similar safety databases
  • Strong understanding of medical terminology and drug safety concepts
  • Ability to handle patient and HCP interactions (including sensitive discussions)
Preferred Qualifications:
  • RN, PharmD, or other healthcare certification
  • Experience with biologics, drugs, or combination products
  • Background in CROs or Pharma/Biotech companies
  • Experience in SOP writing and training delivery
  • Exposure to global pharmacovigilance environments
Top Skills Required:
  • Pharmacovigilance & Adverse Event Case Processing
  • FDA / Health Canada Regulations
  • ARGUS Safety Database
  • Strong communication with patients & HCPs
  • Critical thinking & escalation judgment
Soft Skills:
  • Self-driven and able to work independently in remote setup
  • Strong communication and collaboration skills
  • Ability to handle high-volume workload and prioritize effectively
  • Comfortable in externally facing, high-visibility role
Nice-to-Have Background:
  • CROs: IQVIA, Parexel, ICON, Syneos, PPD, Labcorp
  • Pharma/Biotech: Pfizer, Amgen, Novartis, AbbVie, Merck
Interview Process:
  • Round 1: Hiring Manager (Nancy Dubois)
  • Round 2: Senior Pharmacovigilance Team
Additional Notes:
  • Immediate need due to high case volume and understaffing
  • Role is highly visible and interactive, not just backend processing
  • Potential for future conversion (must be open to hybrid in TX or MA)

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