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Pharmacovigilance Jobs (NOW HIRING)

Med Communications

Pharmacovigilance Physician

Pharmacovigilance Reports To: Global Head of Pharmacovigilance and Drug Safety Employment Type: Contractor Join our Team Med Communications is seeking a Pharmacovigilance Physician (MD, DO, or ...

AA2IT

Pharmacovigilance

North Wales, PA · On-site

Pharmacovigilance Safety Specialist Education: Bachelor's degree or Master's degree or Advance level degree in a life science/healthcare/pharmaceutical related field. Required: Candidate is required ...

Fladger Associates

Pharmacovigilance (PV)

Boston, MA · On-site

Excellent employment opportunity for a Pharmacovigilance (PV) in the Boston, MA area. * We are looking for a Pharmacovigilance Scientist (approximately 25 hours per week) who can support us in ...

VENESCO LLC

Pharmacovigilance Physician

Frederick, MD · On-site

Pharmacovigilance Physician Venesco is seeking a Pharmacovigilance Physician to provide medical oversight and clinical expertise for all safety surveillance and pharmacovigilance activities. The ...

W.F. Young, Inc.

Veterinarian, Pharmacovigilance

Duluth, GA · On-site

$90 - $110/hr

The Veterinarian, Pharmacovigilance ensures pharmacovigilance compliance with all competent authorities (including but not limited to FDA, USDA‑APHIS, EMA, CFIA etc.) as described in the corporate ...

New

Umoja Biopharma

Director, Pharmacovigilance

$204K - $305K/yr

The Director of Pharmacovigilance (PV) will play a critical role in executing Umoja Biopharma's global safety strategy across clinical-stage programs. This individual will be responsible for day-to ...

ICON

Senior Pharmacovigilance Associate

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 ...

YO AI Labs

Pharmacovigilance Expert - Remote

San Jose, CA · Remote

$70 - $80/hr

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 ...

YO AI Labs

Pharmacovigilance Expert - Remote

Atlanta, GA · Remote

$70 - $80/hr

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 ...

YO AI Labs

Pharmacovigilance Expert - Remote

Chicago, IL · Remote

$70 - $80/hr

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 ...

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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.
More about pharmacovigilance jobs

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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:

What job categories do people searching Pharmacovigilance jobs look for?

The top searched job categories for Pharmacovigilance jobs are:

pharmacovigilance jobs near you
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.

Pharmacovigilance Specialist

Rishabh RPO

Los Angeles, CA • On-site

Contractor

Re-posted 9 days ago

Job description

Title: Pharmacovigilance Specialist

Location: Los Angeles, CA 90032

Duration- 4 months (Possible extension for long term)

FAQ
This position is for Adverse event monitoring. This person will deal with marketed products and side effects, follow up with reporters (patients, Doctors, etc.), and triage case reports. Looking for someone with a background in Pharmacovigilance who can follow international regulatory guidelines.
Preference is for the ARGUS database. PSUR exp would be nice.

The interview will consist of a phone screen with the local manager and a second phone screen with management in Barcelona. The team is based in LA, but it is a global team and will need someone who can be flexible in scheduling meetings across multiple time zones.

Summary:

  • Provides operational support for global pharmacovigilance activities of client's marketed products.
  • Ensures pharmacovigilance deliverables are of the highest quality and meet global regulatory reporting timelines.
  • Responsible for data review, compilation, and analysis, including management of the integrated safety database.
Primary responsibilities for the role:
  • Management of Adverse Events including activities such as processing adverse event case reports and conducts follow-up .
  • Notifies regulatory agencies and business partners accordingly; responds to requests from regulatory agencies
  • Reviews scientific literature and bibliographic sources; draft and manage periodic safety update reports. .
  • Evaluates safety profiles; draft and manage signal detection reports; ensures document filing and archiving. .
  • Participation in the processes involving the collection, processing, review and distribution of adverse event information regarding development and marketed client's pharmaceutical products. .
  • Contributes to ensure compliance of pharmacovigilance activities including activities such as conduct case reconciliation with concerned departments, affiliates, distributors or business partners .
  • Take part in self-inspection visits, audits, inspections and in CAPAs management, create or update pharmacovigilance procedures and working practices .
  • Provide training to concerned persons based on the training plan and managing training documentation; archive documents according to prevailing standards .
  • Support in the procedures of global pharmacovigilance operations such as Standard Operation Procedures (SOPs), internal business practices or working instructions. .
  • Serves in an advisory capacity including activities such as product monographs review, draft responses to pharmacovigilance requests from regulatory agencies; participates in the drafting and implementation of pharmacovigilance contracts and agreements. be sure to see notes before submitting candidates.

Questions to be answered

  1. List specific areas of expertise in Pharmacovigilance you have focused on.
  2. What safety database(s) have you used, and what types of cases have you processed?
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About Rishabh BPO Services

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Rishabh BPO is the right choice for companies looking to outsource their business processes to lower their costs, eventually resulting in a transformation of the way the company works. The general benefits of BPO are well known in the industry today. Long term approach of engaging with the customers: This means that Rishabh BPO will focus on getting value for their customers by investing their own resources in the short-term so that the clients experience the value of working with Rishabh BPO over the entire engagement.

Industry

Business management consulting

Company size

51 - 200 Employees

Headquarters location

San Jose, CA, US

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