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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 ...

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Pharmacovigilance information

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How much do pharmacovigilance jobs pay per hour?

As of Jul 28, 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 qualifications do I need for pharmacovigilance?

Pharmacovigilance professionals typically need a bachelor's degree in pharmacy, medicine, life sciences, or a related field. Relevant skills include knowledge of drug safety regulations, data analysis, and experience with safety databases or reporting tools; certifications such as the Drug Safety Certification (DSC) can enhance job prospects.

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.

What is the highest salary in pharmacovigilance?

The highest salaries in pharmacovigilance roles can exceed $150,000 annually, especially for senior positions such as PV managers or directors with extensive experience, certifications, and leadership responsibilities. Salaries vary based on location, company size, and individual expertise, with top earners often working in pharmaceutical or biotech industries in major markets.

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.

Is pharmacovigilance a good career?

Pharmacovigilance is a growing field focused on monitoring drug safety and adverse effects, offering opportunities in pharmaceutical companies, CROs, and regulatory agencies. It requires strong analytical skills, attention to detail, and knowledge of medical and regulatory guidelines. The career can be stable with potential for advancement and specialization, especially with relevant certifications and experience.

What is the job role in pharmacovigilance?

A pharmacovigilance job involves monitoring, detecting, assessing, and reporting adverse drug reactions and safety issues related to pharmaceutical products. Professionals in this field analyze data from clinical trials and post-marketing surveillance, often using specialized software, to ensure medication safety and compliance with regulatory requirements.

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

To thrive in Pharmacovigilance, you need a background in pharmacy, life sciences, or medicine, along with a strong understanding of drug safety regulations and adverse event reporting. Familiarity with pharmacovigilance databases (such as Argus or ARISg), MedDRA coding, and relevant regulatory guidelines (like ICH and FDA) is typically required. Attention to detail, analytical thinking, and effective communication are vital soft skills for accurately evaluating and reporting safety data. These competencies ensure the integrity of drug safety monitoring, compliance with global regulations, and the protection of public health.

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 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.
More about Pharmacovigilance jobs
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:
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 July 2026, with employment types broken down into 96% Full Time, 1% Part Time, and 3% Contract. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $96,145 per year, or $46.2 per hour.
Pharmacovigilance Specialist

Pharmacovigilance Specialist

Rishabh RPO

Los Angeles, CA • On-site

Contractor

Posted 17 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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