ZipRecruiter

Log In

1

Pharmacovigilance Associate Jobs (NOW HIRING)

next page

Showing results 1-20

All JobsPharmacovigilance Associate Jobs

Pharmacovigilance Associate information

See salary details

$12

$49

$85

How much do pharmacovigilance associate jobs pay per hour?

As of Jun 15, 2026, the average hourly pay for pharmacovigilance associate in the United States is $49.14, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $55.53 per hour, depending on experience, location, and employer.

What are the typical daily responsibilities of a Pharmacovigilance Associate?

A Pharmacovigilance Associate is responsible for collecting, reviewing, and processing reports of adverse drug reactions, ensuring that all data is accurate and submitted in accordance with regulatory timelines. On a daily basis, you may enter case information into specialized safety databases, conduct follow-ups with healthcare professionals or patients for additional details, and assist in preparing safety reports for regulatory authorities. The role often involves close collaboration with medical, regulatory, and quality assurance teams to support comprehensive drug safety monitoring. You may also participate in ongoing training or audits to maintain compliance with evolving industry standards.

What do pharmacovigilance associates do?

Pharmacovigilance associates monitor, collect, and analyze data on adverse drug reactions and medication safety. They review reports, ensure compliance with regulatory requirements, and support risk management activities using databases and safety tools. Their work helps ensure the safety of pharmaceutical products throughout their lifecycle.

What are the key skills and qualifications needed to thrive in the Pharmacovigilance Associate position, and why are they important?

To thrive as a Pharmacovigilance Associate, you need a strong background in life sciences or pharmacy, attention to detail, and a solid understanding of drug safety regulations. Familiarity with safety databases such as Argus or ARISg, as well as knowledge of global regulatory guidelines like FDA and EMA requirements, is often required. Strong analytical thinking, effective communication, and organizational skills help you manage case reports and collaborate with cross-functional teams. These skills are essential for accurately assessing and reporting adverse drug reactions to ensure patient safety and regulatory compliance.

What is a Pharmacovigilance Associate job?

A Pharmacovigilance Associate is responsible for monitoring, collecting, assessing, and reporting adverse drug reactions (ADRs) to ensure patient safety. They work with regulatory authorities, healthcare professionals, and pharmaceutical companies to analyze drug safety data. Their duties include case processing, literature screening, signal detection, and ensuring compliance with pharmacovigilance regulations. This role is vital for minimizing drug-related risks and maintaining regulatory compliance.

What is the average salary for a pharmacovigilance Associate?

The average salary for a pharmacovigilance associate in the US typically ranges from $60,000 to $80,000 per year, depending on experience, location, and certifications. Entry-level positions may start lower, while experienced professionals with specialized skills can earn higher salaries, often with opportunities for bonuses and benefits.

What skills are required for a pharmacovigilance associate position?

A pharmacovigilance associate needs strong attention to detail, good communication skills, and knowledge of regulatory guidelines such as ICH and GVP. Proficiency in data management tools, medical terminology, and basic understanding of drug safety processes are also essential. Often, a background in life sciences or pharmacy is required, along with the ability to work in a regulated environment.

Is pharmacovigilance a good career?

Pharmacovigilance is a growing field that involves monitoring the safety of pharmaceutical products, making it a stable career option with demand in the healthcare and pharmaceutical industries. It requires attention to detail, knowledge of regulatory guidelines, and often involves working with safety databases and reporting tools. Many professionals find it a rewarding career due to its impact on public health and opportunities for specialization and advancement.
More about Pharmacovigilance Associate jobs
What cities are hiring for Pharmacovigilance Associate jobs? Cities with the most Pharmacovigilance Associate job openings:
What are the most commonly searched types of Pharmacovigilance jobs? The most popular types of Pharmacovigilance jobs are:
Who are the top companies hiring for Pharmacovigilance Associate jobs? The top employers for Pharmacovigilance Associate jobs are:
What states have the most Pharmacovigilance Associate jobs? States with the most job openings for Pharmacovigilance Associate jobs include:
What job categories do people searching Pharmacovigilance Associate jobs look for? The top searched job categories for Pharmacovigilance Associate jobs are:
Pharmacovigilance Associate jobs near you
Infographic showing various Pharmacovigilance Associate job openings in the United States as of June 2026, with employment types broken down into 3% As Needed, 94% Part Time, and 3% Contract. Highlights an 80% Physical, 4% Hybrid, and 16% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

Vice President, Safety & Pharmacovigilance

Fore Biotherapeutics US Inc

Philadelphia, PA • On-site

Full-time

Posted 11 days ago

Job description

Role Summary:

Fore Bio is a next-generation precision oncology company focused on the development of plixorafenib, an investigational, novel, small-molecule, next-generation, orally available selective inhibitor of mutated BRAF.

The VP, Safety and Pharmacovigilance will be responsible for leading the safety and risk assessment of the product portfolio at all stages of the product lifecycle, including ensuring compliance with health authority regulations in all aspects of pharmacovigilance case reporting and processing.

Essential Duties and Responsibilities:

  • Accountable for providing medical and scientific expertise regarding the safety and risk assessment of the product portfolio at all stages of the product lifecycle.
  • Foresight for the growth and oversight of the Pharmacovigilance department, including building and managing a team of medical professionals (at various levels of expertise) to implement the development strategy and support registrational and post-marketing activities in a compliant and collaborative environment, in accordance with long-term strategic goals
  • Defines and implements methods for the collection, evaluation, management, and communication of safety data from all sources regarding products in development. Ensures applicable review and oversight of Pharmacovigilance systems in all aspects, including database, SOPs, training and compliance, and audits and activities performed by vendors.
  • Responsible for medical safety deliverables that may be the subject of regulatory inspections, including preparation of medical safety documentation, and follow-up activities such as responses and CAPA development and implementation.
  • Responsible for the aggregate review of data for safety signal detection. Performs/oversees signal detection activities and provides written reports to Senior Management. Develops and implements risk management plans in accordance with regulatory requirements. Collaborates with Nonclinical and with Clinical to better assess and understand safety profiles and to prepare safety surveillance activities. Author aggregate reports and benefit/risk assessments.
  • Medical expert responsible for safety in the following documents: regulatory responses, Investigator’s Brochure (IBs) including the development of the reference safety information (RSI); standardized safety language for informed consent forms (ICFs), study protocols, and other pharmacovigilance related documents (e.g. DSUR).
  • Manages and reviews/oversees reconciliation SAE data between clinical and safety databases.
  • Maintains the highest standards and levels of scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment. Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research.
  • Ensures compliance with health authority regulations in all aspects of PV safety operations, case processing and reporting; tracks compliance of expedited safety reports in relation with Pharmacovigilance vendors.


Education and/or Work Experience Requirements:

  • Medical Degree (MD) with outstanding relevant experience. Possess a minimum of 15 years experience in pharmaceutical/ biotech with risk management and Pharmacovigilance (safety signal detection, data mining techniques, pharmacovigilance databases, etc.); expertise in Oncology preferred
  • Expertise in international regulations governing drug safety
  • Extensive knowledge of regulatory and compliance requirements governing clinical safety, as well as overall understanding and knowledge of NDA and global filing requirements.
  • Proven track record in creating and sustaining a leading‐edge, high quality Pharmacovigilance function within the complex global regulatory-pharmacovigilance environment.
  • Proven prior experience with guiding Safety & Pharmacovigilance team through NDA and commercialization.
  • Ability to comprehend and synthesize complex data and experience in the identification, analysis and implementation of programs and procedures required to achieve corporate objectives.
  • Demonstrated ability to recognize and anticipate problems and proactively resolve them. Strong track record of enjoying the details without losing sight of the larger goals. Ability to multi-task and handle multiple projects simultaneously.
  • Excellent technical writing, oral, presentation, and interpersonal communication skills and ability to present concepts and results in a clear and concise manner.
  • Highly motivated, decisive, and results-oriented individual with the flexibility and creativity to excel in and contribute to a rapidly growing company.


Fore is an Equal Opportunity Employer. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic

Apply