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How much do associate director pharmacovigilance jobs pay per year?

As of Aug 7, 2026, the average yearly pay for associate director pharmacovigilance in the United States is $164,797.00, according to ZipRecruiter salary data. Most workers in this role earn between $121,500.00 and $200,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an associate director pharmacovigilance, and why are they important?

To thrive as an Associate Director Pharmacovigilance, you need in-depth knowledge of drug safety regulations, clinical development, and risk management, typically supported by an advanced degree in life sciences or pharmacy. Familiarity with pharmacovigilance databases (such as Argus or ARISg), regulatory reporting systems, and certifications like RAPS or DIA are commonly required. Exceptional leadership, analytical thinking, and strong communication skills set standout candidates apart. These abilities ensure effective oversight of drug safety operations, regulatory compliance, and timely risk mitigation for patient safety.

What does an associate director pharmacovigilance do?

An Associate Director of Pharmacovigilance is responsible for overseeing drug safety activities, ensuring compliance with global pharmacovigilance regulations, and managing safety data collection, analysis, and reporting. They lead teams that monitor and evaluate adverse events related to pharmaceutical products, work closely with regulatory authorities, and help develop risk management strategies. Their work is crucial in maintaining drug safety and ensuring patient well-being throughout the product lifecycle.

How does an associate director pharmacovigilance typically collaborate with cross-functional teams within a pharmaceutical company?

As an Associate Director of Pharmacovigilance, you will regularly collaborate with teams across clinical development, regulatory affairs, medical affairs, and quality assurance. Your role often involves leading safety review meetings, coordinating safety data exchange agreements, and ensuring timely communication of safety information both internally and to regulatory authorities. This cross-functional collaboration is essential for maintaining compliance with global safety regulations and for supporting the safe development and commercialization of pharmaceutical products. Building strong relationships and clear lines of communication with these teams will be crucial to your success and impact in the role.
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Associate Director Pharmacovigilance jobs near you
Infographic showing various Associate Director Pharmacovigilance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $164,797 per year, or $79.2 per hour.

Associate Director, Pharmacovigilance Scientist

Deciphera Pharmaceuticals

Waltham, MA • On-site, Remote

$162K - $223K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 5 days ago

Job description

Company Description
Job Description
The Associate Director, Pharmacovigilance Scientist plays a critical role in safety data analyses for assigned investigational and/or marketed product(s) in partnership with the Safety Physician. This individual also serves as a subject matter expert for the PV Sciences group, contributing to strategic initiatives in collaboration with key stakeholders.
The Associate Director, Pharmacovigilance Scientist is expected to be equally effective in working collaboratively and independently. She/he will be responsible for leading and/or contributing to activities such as signal management, aggregate reports, RMP development, ad hoc safety query responses, literature surveillance, and safety analyses for regulatory submissions (NDA, MAA, etc.). For investigational products, this role may also encompass contributions to IB/RSIs, ICFs, SMPs, DMC materials, coding reviews, and safety analyses for CSRs, as applicable. The Associate Director, Pharmacovigilance Scientist will also contribute to process improvement initiatives, lead strategic innovations, and manage/mentor others, as opportunities permit.
Key Responsibilities
Serves as lead PV Scientist for assigned product(s) - 60%
  • Conducts signal detection, evaluation, and management, including data coordination, analysis, presentation, and documentation
  • Leads and manages the planning, preparation, writing, and review of aggregate safety reports (DSURs, PADERs, PBRERs)
  • Leads and manages the planning, preparation, writing, and review of risk management plans
  • Performs literature surveillance
  • Prepares materials for safety governance meetings
  • Contributes to safety-related regulatory queries, including data coordination and analysis
  • Contributes to relevant sections of key documents (IB/RSIs, CCDS/labels, ICF, DMC materials, coding reviews, CSRs, etc., as applicable)
  • Contributes to safety analyses associated with regulatory filings (e.g., New Drug Applications or Marketing Authorization Applications)
  • Supports team in proactively maintaining inspection readiness and serves as a subject matter expert in the event of an inspection

Other functional and cross-functional initiatives - 25%
  • Leads strategic innovations (streamlines processes, evaluates implementation of new technology and resources, etc.)
  • Conducts impact assessments (e.g., updates to regulations, etc.)
  • Leads process improvement initiatives and consistency of cross-product processes
  • Conducts functional trainings and shares knowledge with the team
  • Supports deliverables for other products, where needed

Management and mentorship - 15%
  • Manages, mentors, and trains junior members of the team
  • Supports individual development of direct reports

Other duties and responsibilities as assigned
Qualifications
Required Qualifications:
  • Minimum 5-6 years PV experience, including a minimum of 3-4 years in a PV Scientist or similar role
  • Advanced degree (PharmD, RN, MD, PhD, MPH, NP, MS)
  • Demonstrated experience in analysis and interpretation of medical and scientific data, including experience leading signal management activities and the preparation and authoring of aggregate reports in both post-marketing and clinical trials
  • Excellent oral and written communication skills, including the ability to effectively communicate key considerations and decision points
  • Detail-oriented with ability to think critically, prioritize tasks, and function independently
  • Expert knowledge of pharmacovigilance and drug development, including knowledge of applicable clinical trial and post-marketing safety regulations
  • Proven track record in preparing and reviewing regulatory safety documents, including NDAs/MAAs and RMPs
  • Prior experience serving as an SME in audits and/or inspections

Preferred Capabilities:
  • Demonstrated experience in various therapeutic areas (e.g., oncology, CNS, etc.)
  • Expert proficiency with pharmacovigilance databases and relevant coding dictionaries
  • Expert knowledge/proficiency with Microsoft Office Suite and Argus Safety systems

Additional Information
Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $162,000 - $223,000. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location.
Deciphera believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Deciphera's competitive total rewards strategy that also includes annual performance bonus, a long-term incentive plan, full range of benefits and other incentive compensation plans (if applicable)
Benefits:
  • Competitive salary and annual bonus.
  • Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more.
  • Generous parental leave and family planning benefits.
  • Outstanding culture and opportunities for personal and professional growth.

Apply Now: Join us in our mission to improve the lives of people with cancer. Apply today to become a part of our dynamic team!
EQUAL EMPLOYMENT OPPORTUNITY INFORMATION
Deciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements, we invite you complete the confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. We are committed to make all hiring decisions and other employment decisions on a non-discriminatory basis.
EQUAL EMPLOYMENT OPPORTUNITY INFORMATION
Deciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements, we invite you complete the confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. We are committed to make all hiring decisions and other employment decisions on a non-discriminatory basis.

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