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Pharmacovigilance Jobs (NOW HIRING)

Pharmacovigilance Expert Job Type: Contractor Location: Remote Job Overview We are seeking experienced Pharmacovigilance Experts to contribute their drug safety expertise to an innovative healthcare ...

Pharmacovigilance Expert Job Type: Contractor Location: Remote Job Overview We are seeking experienced Pharmacovigilance Experts to contribute their drug safety expertise to an innovative healthcare ...

Senior Pharmacovigilance Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...

Director, Pharmacovigilance

Seattle, WA ยท On-site

$110 - $180/hr

Contribute to development and maintenance of SOPs and Pharmacovigilance System Master File (PSMF) Requirements * Advanced degree (PharmD, PhD, MD, or MS) or healthโ€‘related degree/certification (PA ...

Pharmacovigilance Specialist In Italy Pharmacovigilance Specialist is responsible for assuring compliance with local and regional Quality Management System and interact, exchange relevant safety and ...

Pharmacovigilance Expert Job Type: Contractor Location: Remote Job Overview We are seeking experienced Pharmacovigilance Experts to contribute their drug safety expertise to an innovative healthcare ...

Pharmacovigilance Expert

Cincinnati, OH ยท Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role ...

Pharmacovigilance Expert

Providence, RI ยท Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role ...

Pharmacovigilance Expert

Greensboro, NC ยท Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role ...

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role ...

Pharmacovigilance Expert

Surprise, AZ ยท Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role ...

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role ...

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pharmacovigilance information

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How much do pharmacovigilance jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for pharmacovigilance in the United States is $46.22, according to ZipRecruiter salary data. Most workers in this role earn between $26.92 and $55.29 per hour, depending on experience, location, and employer.

What is pharmacovigilance?

Pharmacovigilance is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. It plays a crucial role in ensuring the safety and efficacy of medicines once they are released on the market. Professionals in pharmacovigilance monitor reports of side effects and work with healthcare providers, regulatory agencies, and pharmaceutical companies to minimize risks to patients. This field helps maintain public health by identifying potential issues with medications and recommending actions such as warnings, restrictions, or even withdrawal of drugs if necessary.

What are pharmacovigilance jobs?

Pharmacovigilance positions may include a drug safety associate, drug safety scientist, drug safety manager or director, pharmaceutical information specialist, and related positions such as administrative positions and technical writers who specialize in pharmacovigilance writing. The duties of drug safety scientists and associates are to perform research, monitor trials, and investigate adverse effect reports. Information specialists record, categorize and store data related to drugs. Pharmacovigilance directors oversee pharmacovigilance operations, communicate with physicians, drug makers, and regulators when necessary, and ensure compliance with regulations.

What are some common challenges faced by professionals in pharmacovigilance, and how can they be addressed?

Pharmacovigilance professionals often encounter challenges such as managing large volumes of safety data, staying updated with evolving global regulations, and ensuring clear communication across multidisciplinary teams. Addressing these challenges typically involves continuous training, leveraging advanced data management tools, and fostering strong collaboration with regulatory, clinical, and medical affairs teams. Proactively engaging in professional development and adopting best practices in data analysis and reporting can also help professionals navigate these complexities effectively.

What is the difference between Pharmacovigilance vs Drug Safety Associate?

AspectPharmacovigilanceDrug Safety Associate
CredentialsTypically requires a degree in pharmacy, life sciences, or related fields; certifications like PV or drug safety training are commonSimilar educational background; often requires training in drug safety and pharmacovigilance practices
Work EnvironmentPharmacovigilance professionals often work in pharmaceutical companies, CROs, or regulatory agencies, focusing on safety data analysisDrug Safety Associates usually work in similar settings, handling case processing and safety reporting
Industry UsageUsed broadly across pharma, biotech, and regulatory sectors for safety monitoringPrimarily used within pharmaceutical companies and CROs for case management and reporting

Both roles focus on drug safety, with pharmacovigilance encompassing a broader scope of safety monitoring, analysis, and regulatory compliance, while Drug Safety Associates typically handle case processing and reporting tasks within that framework.

How much do pharmacovigilance jobs pay in the US?

Pharmacovigilance jobs in the US typically offer salaries ranging from $70,000 to $120,000 annually, depending on experience, education, and location. Entry-level positions may start around $60,000, while senior roles with specialized skills or certifications can exceed $130,000.

Is pharmacovigilance a good career option?

Pharmacovigilance is a growing field focused on monitoring the safety of medicines, offering opportunities for careers in drug safety, data analysis, and regulatory compliance. It typically requires knowledge of pharmacology, good communication skills, and familiarity with safety databases and regulations. The profession provides stable employment with potential for advancement in pharmaceutical and healthcare industries.

What cities are hiring for Pharmacovigilance jobs?

Cities with the most Pharmacovigilance job openings:

What are the most commonly searched types of Pharmacovigilance jobs?

The most popular types of Pharmacovigilance jobs are:

What states have the most Pharmacovigilance jobs?

States with the most job openings for Pharmacovigilance jobs include:

Infographic showing various Pharmacovigilance job openings in the United States as of August 2026, with employment types broken down into 71% Full Time, 25% Part Time, and 4% Contract. Highlights an 56% Physical, 3% Hybrid, and 41% Remote job distribution, with an average salary of $96,145 per year, or $46.2 per hour.

Vice President, Pharmacovigilance

Deciphera Pharmaceuticals

Waltham, MA โ€ข On-site, Remote

$335K - $460K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 22 days ago


Job description

Company Description
Job Description
We are seeking a strategic and accomplished Vice President, Pharmacovigilance to lead Deciphera's global drug safety and pharmacovigilance function. This executive leader will be accountable for patient safety, regulatory compliance, and proactive benefit-risk assessment across investigational and marketed products. The VP will set the vision for safety governance, product safety strategy, risk management, regulatory safety support, and pharmacovigilance operations while partnering closely across Clinical Development, Regulatory Affairs, Medical Affairs, Quality, Commercial, Technical Operations, and other key functions.
What You'll Do
  • Develop and execute the global pharmacovigilance strategy in alignment with corporate objectives, regulatory requirements, and Deciphera's commitment to patient safety.
  • Provide executive leadership for benefit-risk evaluation, safety governance, safety surveillance, signal management, and risk management across investigational and marketed products.
  • Serve as a senior safety advisor to executive leadership and represent Pharmacovigilance in governance committees, leadership forums, and interactions with health authorities.
  • Ensure global pharmacovigilance activities are compliant, inspection-ready, scientifically rigorous, and aligned with applicable regulatory requirements, GCP standards, and internal quality systems.
  • Establish and evolve scalable pharmacovigilance systems, processes, quality frameworks, vendor partnerships, and operational capabilities to support a growing global portfolio.
  • Build, develop, and lead a high-performing pharmacovigilance organization while fostering a culture of scientific excellence, accountability, collaboration, and patient-focused decision making.

Qualifications
  • MD, DO, PharmD, PhD, or equivalent advanced scientific or healthcare degree.
  • 15+ years of progressive experience in pharmacovigilance, clinical safety, drug safety, or drug development within the biotechnology or pharmaceutical industry.
  • 8+ years of leadership experience managing global pharmacovigilance, clinical safety, or patient safety organizations.
  • Demonstrated experience supporting products across clinical development and commercialization.
  • Deep understanding of global pharmacovigilance regulations, guidelines, and industry best practices, including FDA, EMA, ICH, GCP, and other applicable requirements.
  • Experience with safety governance, benefit-risk assessment, signal detection, risk management, safety reporting, and inspection readiness.
  • Track record of successful health authority interactions, regulatory inspections, audits, and cross-functional safety leadership.
  • Strong strategic leadership, communication, decision-making, and stakeholder management skills.

Preferred Experience
  • Oncology experience strongly preferred.
  • Experience supporting small molecule therapeutics.
  • Prior experience leading pharmacovigilance activities for commercial-stage products.
  • Experience working in a global, outsourced operating model utilizing CROs and external pharmacovigilance vendors.
  • Demonstrated success building, scaling, and evolving pharmacovigilance organizations, systems, and operating models.
  • Experience supporting regulatory submissions, product launches, and post-marketing safety activities in multiple global markets.
  • Strong business acumen with the ability to align safety strategy with corporate objectives.

Additional Information
Additional Information
Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $335,000-$460,000. 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.

Equal Employment Opportunity Information
Deciphera is committed to equal employment opportunity and values diversity. To help us meet reporting requirements, we invite you to complete the confidential survey at the end of this application. Providing this information is entirely optional. It will not be used in the hiring process and will have no impact on your opportunity for employment. The information will be treated confidentially. Deciphera is committed to making all hiring and employment decisions fairly and 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.