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Contract Pharmacovigilance Jobs (NOW HIRING)

Med Communications

Pharmacovigilance Physician

Pharmacovigilance Reports To: Global Head of Pharmacovigilance and Drug Safety Employment Type ... contracts. What We're Looking For Education Either: * Licensed Medical Physician (MD, DO, or ...

Virbac Group

WI · On-site

$120 - $180/hr

## Veterinary Pharmacovigilance ManagerApplylocations: Westlake TX, USAtime type: Full timeposted on ... contract negotiations)*Expected results: Helps department remain in compliance with all company ...

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How much do contract pharmacovigilance jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for contract 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 a contract pharmacovigilance?

A Contract Pharmacovigilance job involves monitoring, assessing, and reporting adverse drug reactions (ADRs) and ensuring compliance with regulatory safety requirements on a contractual basis. Professionals in this role may work for pharmaceutical companies, contract research organizations (CROs), or as independent consultants. Responsibilities typically include case processing, signal detection, risk management, and regulatory reporting. Contract roles offer flexibility in workload, duration, and employer, making them an attractive option for experienced pharmacovigilance professionals.

What does a contract pharmacovigilance professional do?

As a Contract Pharmacovigilance professional, your typical day may involve monitoring and processing adverse event reports, conducting safety data reviews, and preparing regulatory submissions within specified timelines. You’ll often collaborate closely with clinical teams, regulatory affairs, and external partners to ensure that safety information is accurately captured and communicated. Tasks may also include maintaining safety databases, supporting audit readiness, and keeping up-to-date with changing global regulations. This dynamic role requires balancing multiple projects and adapting quickly to shifting priorities, making strong organizational and communication skills especially valuable.

What are the key skills and qualifications needed for contract pharmacovigilance?

To thrive as a Contract Pharmacovigilance professional, you need a solid background in pharmaceutical sciences, data analysis, and adverse event reporting, typically supported by a relevant degree in pharmacy, life sciences, or a related field. Familiarity with safety databases (such as Oracle Argus or ArisGlobal), knowledge of regulatory guidelines (like FDA and EMA), and certifications in Good Pharmacovigilance Practices (GVP) are highly valuable. Strong attention to detail, effective communication, and the ability to collaborate with cross-functional teams are standout soft skills in this role. These skills are essential for ensuring patient safety, regulatory compliance, and timely completion of contractual pharmacovigilance deliverables.

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Contract Pharmacovigilance jobs near you
Infographic showing various Contract Pharmacovigilance job openings in the United States as of August 2026, with employment types broken down into 96% Full Time, 1% Part Time, and 3% Contract. Highlights an 71% Physical, 4% Hybrid, and 25% Remote job distribution, with an average salary of $96,145 per year, or $46.2 per hour.

Pharmacovigilance Specialist (Contract)

Unicon Pharma Inc.

Austin, TX • Remote

$50 - $55/hr

Contractor

Re-posted 7 days ago

Job description

Description:
 
Pharmacovigilance Specialist
Remote
Until end of the year (possible extension)
 
Plays a key operational support role in the GRADS Global Risk Management Team, supporting the development, implementation, execution, and monitoring of risk management activities, assessments, and documents for client product(s) in Canada. This role will collaborate cross-functionally (e.g., with the Safety Management Team, QPPV, other functions, and affiliates) and will support process development, training, and continuous improvement efforts.
Essential Functions/Responsibilities
• Provide operational support to risk management activities for Client products in Canada.
• Contribute to developing/updating training and communication materials, including delivering training or roadshows on risk management processes to other business functions to foster awareness of risk management practices.
• Contribute to inspection readiness activities.
• Support the design, implementation, and/or evaluation of additional pharmacovigilance activities and additional risk minimization measures.
• Maintain awareness of regulatory intelligence pertaining to risk management.
• Represent Global Risk Management in cross-functional teams/forums.
• Develop/update processes and implement changes in collaboration with other business functions/affiliates in an evolving regulatory environment.
• Develop, coordinate, review, and/or maintain documents that involve risk management (e.g., information requests, reports, safety data exchange agreements) in collaboration with other business functions/affiliates.
• Provide support to global risk management team such as developing project timelines, preparing/archiving agendas, data, slides, and minutes.
• Support data collection, analysis, and reporting for measuring effectiveness of additional pharmacovigilance activities and additional risk minimization measures.
• Identify trends and areas for improvement in risk management practices.
Required Knowledge, Skills, and Abilities
• Knowledge of current and emerging regulatory requirements and expectations pertaining to risk management.
• Knowledge of pharmacovigilance activities and processes. Strong experience with process development.
• Experience managing relationships with service providers or external business partners.
• Excellent teamwork and interpersonal skills with cross-functional team experience.
• Excellent oral and written communications skills.
• Proven ability to demonstrate client values.
• Willingness to take on new challenges/opportunities.
• Ability to work cross culturally both in person and virtually.
• Proficiency with MS Office.
• Familiarity with Smartsheet, Miro.
• Skill in inspiring and guiding others without formal authority.
Required/Preferred Education and Licenses
• BA/BS, MS/MA degree required. Health-related or biological science-related field, PharmD, RPh, or Nursing strongly preferred.
• Minimum of 6 years in pharmacovigilance with risk management experience. Canadian PV experience preferred.
• Operations experience with Compliance (preferred) and/or Quality Assurance.
• Excellent organizational skills with keen attentiveness to detail; project management experience desired.
• Familiarity with PV databases and regulatory information management systems (e.g., Veeva RIM); data management/analysis experience and/or and computer system management experience are a plus.
• Experience with developing and/or managing process documents and/or change controls.