The Manager, Pharmacovigilance - Front End Operations will lead frontline operational support for pharmacovigilance (PV) activities, directly interfacing with Quality Assurance, Patient Solutions ...
The Manager, Pharmacovigilance - Front End Operations will lead frontline operational support for pharmacovigilance (PV) activities, directly interfacing with Quality Assurance, Patient Solutions ...
The Manager, Pharmacovigilance - Front End Operations will lead frontline operational support for pharmacovigilance (PV) activities, directly interfacing with Quality Assurance, Patient Solutions ...
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The Manager, Pharmacovigilance - Front End Operations will lead frontline operational support for pharmacovigilance (PV) activities, directly interfacing with Quality Assurance, Patient Solutions ...
Manager, Pharmacovigilance
Orlando, FL · On-site +1
The Manager, Pharmacovigilance - Front End Operations will lead frontline operational support for pharmacovigilance (PV) activities, directly interfacing with Quality Assurance, Patient Solutions ...
Manager, Pharmacovigilance
Orlando, FL · On-site +1
The Manager, Pharmacovigilance - Front End Operations will lead frontline operational support for pharmacovigilance (PV) activities, directly interfacing with Quality Assurance, Patient Solutions ...
Senior Manager, Pharmacovigilance
San Diego, CA · On-site +1
The Senior Manager of Pharmacovigilance will be responsible for the execution of global pharmacovigilance activities supporting late-stage clinical development and preparation for first commercial ...
Senior Manager, Pharmacovigilance
San Diego, CA · On-site +1
The Senior Manager of Pharmacovigilance will be responsible for the execution of global pharmacovigilance activities supporting late-stage clinical development and preparation for first commercial ...
Senior Manager, Pharmacovigilance - Remote Position Location Los Angeles, CA Department Pharmacovigilance
Senior Manager, Pharmacovigilance - Remote Position Location Los Angeles, CA Department Pharmacovigilance
The Senior Manager of Pharmacovigilance will be responsible for the execution of global pharmacovigilance activities supporting late-stage clinical development and preparation for first commercial ...
Quick apply
The Senior Manager of Pharmacovigilance will be responsible for the execution of global pharmacovigilance activities supporting late-stage clinical development and preparation for first commercial ...
The Senior Manager of Pharmacovigilance will be responsible for the execution of global pharmacovigilance activities supporting late-stage clinical development and preparation for first commercial ...
The Senior Manager of Pharmacovigilance will be responsible for the execution of global pharmacovigilance activities supporting late-stage clinical development and preparation for first commercial ...
Monitor Safety Data Exchange Agreement (SDEA) or Pharmacovigilance Agreement (PVA) with commercial partners * Support development and execution of risk management plans, risk assessment, and risk ...
Monitor Safety Data Exchange Agreement (SDEA) or Pharmacovigilance Agreement (PVA) with commercial partners * Support development and execution of risk management plans, risk assessment, and risk ...
Monitor Safety Data Exchange Agreement (SDEA) or Pharmacovigilance Agreement (PVA) with commercial partners * Support development and execution of risk management plans, risk assessment, and risk ...
Monitor Safety Data Exchange Agreement (SDEA) or Pharmacovigilance Agreement (PVA) with commercial partners * Support development and execution of risk management plans, risk assessment, and risk ...
Requirements: -Oversee operational aspects of the VRC Clinical Trials Program (CTP) Pharmacovigilance (PV) Team, which leads the process for safety signal management activities, and ensures the ...
Requirements: -Oversee operational aspects of the VRC Clinical Trials Program (CTP) Pharmacovigilance (PV) Team, which leads the process for safety signal management activities, and ensures the ...
Alliance and Partnership Manager (Pharmacovigilance Software)
Miami, FL · On-site
$110K - $150K/yr
Our team collaborates with Pharmacovigilance and Risk Management professionals to enhance compliance, productivity, and quality across the drug safety value chain. Dedicated to patient safety and the ...
Alliance and Partnership Manager (Pharmacovigilance Software)
Miami, FL · On-site
$110K - $150K/yr
Our team collaborates with Pharmacovigilance and Risk Management professionals to enhance compliance, productivity, and quality across the drug safety value chain. Dedicated to patient safety and the ...
Our team collaborates with Pharmacovigilance and Risk Management professionals to enhance compliance, productivity, and quality across the drug safety value chain. Dedicated to patient safety and the ...
Our team collaborates with Pharmacovigilance and Risk Management professionals to enhance compliance, productivity, and quality across the drug safety value chain. Dedicated to patient safety and the ...
Workflow Manager, Pharmacovigilance Operations (Specialist II, PSS) US Remote
Durham, NC · Remote
$80K - $105K/yr
Workflow Manager, Pharmacovigilance Operations (Specialist II, PSS) US Remote Fortrea is seeking a Workflow Manager, Pharmacovigilance Operations ( Specialist II, PSS ) is responsible for supporting ...
Workflow Manager, Pharmacovigilance Operations (Specialist II, PSS) US Remote
Durham, NC · Remote
$80K - $105K/yr
Workflow Manager, Pharmacovigilance Operations (Specialist II, PSS) US Remote Fortrea is seeking a Workflow Manager, Pharmacovigilance Operations ( Specialist II, PSS ) is responsible for supporting ...
Our team collaborates with Pharmacovigilance and Risk Management professionals to enhance compliance, productivity, and quality across the drug safety value chain. Dedicated to patient safety and the ...
Quick apply
Our team collaborates with Pharmacovigilance and Risk Management professionals to enhance compliance, productivity, and quality across the drug safety value chain. Dedicated to patient safety and the ...
Specialist, Pharmacovigilance
Pittsburgh, PA · On-site
$18.96 - $25.85/hr
Under direct supervision of the department manager or supervisor, the Specialist, Pharmacovigilance is focused on meeting ConnectiveRx's obligations for Drug Safety Monitoring and Reporting as ...
Specialist, Pharmacovigilance
Pittsburgh, PA · On-site
$18.96 - $25.85/hr
Under direct supervision of the department manager or supervisor, the Specialist, Pharmacovigilance is focused on meeting ConnectiveRx's obligations for Drug Safety Monitoring and Reporting as ...
Under direct supervision of the department manager or supervisor, the Specialist, Pharmacovigilance is focused on meeting ConnectiveRx's obligations for Drug Safety Monitoring and Reporting as ...
Under direct supervision of the department manager or supervisor, the Specialist, Pharmacovigilance is focused on meeting ConnectiveRx's obligations for Drug Safety Monitoring and Reporting as ...
Under direct supervision of the department manager or supervisor, the Specialist, Pharmacovigilance is focused on meeting ConnectiveRx's obligations for Drug Safety Monitoring and Reporting as ...
Under direct supervision of the department manager or supervisor, the Specialist, Pharmacovigilance is focused on meeting ConnectiveRx's obligations for Drug Safety Monitoring and Reporting as ...
Pharmacovigilance Manager Location: Dayton, NJ Duration: ( Right to Hire) Fulltime Permanent Our Client is looking for Pharmacovigilance Manager- with 1 year of experience.....!!!!! JOB SUMMARY: This ...
Pharmacovigilance Manager Location: Dayton, NJ Duration: ( Right to Hire) Fulltime Permanent Our Client is looking for Pharmacovigilance Manager- with 1 year of experience.....!!!!! JOB SUMMARY: This ...
Responsibilities Oversee investigational and postmarketing regulatory reporting and pharmacovigilance activities for assigned Global products Lead the development and execution of risk management ...
Responsibilities Oversee investigational and postmarketing regulatory reporting and pharmacovigilance activities for assigned Global products Lead the development and execution of risk management ...
Lead and manage pharmacovigilance activities within a specific workstream or therapeutic area, ensuring alignment with organizational objectives and regulatory standards. * Responsible for generating ...
Quick apply
Lead and manage pharmacovigilance activities within a specific workstream or therapeutic area, ensuring alignment with organizational objectives and regulatory standards. * Responsible for generating ...
Manager Pharmacovigilance information
See salary details
$13K - $30.9K
0% of jobs
$30.9K - $48.8K
0% of jobs
$48.8K - $66.7K
0% of jobs
$66.7K - $84.6K
1% of jobs
$84.6K - $102.5K
1% of jobs
$102.5K - $120.5K
8% of jobs
$130.3K is the 25th percentile. Wages below this are outliers.
$120.5K - $138.4K
28% of jobs
The median wage is $147.3K / yr.
$138.4K - $156.3K
25% of jobs
$168.7K is the 75th percentile. Wages above this are outliers.
$156.3K - $174.2K
18% of jobs
$174.2K - $192.1K
12% of jobs
$192.1K - $210K
8% of jobs
$13K
$150.5K
$210K
How much do manager pharmacovigilance jobs pay per year?
What is a Manager Pharmacovigilance job?
A Manager Pharmacovigilance oversees drug safety monitoring, ensuring compliance with regulatory requirements and company policies. They manage adverse event reporting, risk assessments, and signal detection to identify potential safety concerns. This role involves collaborating with cross-functional teams, regulatory authorities, and healthcare professionals. Strong knowledge of global pharmacovigilance regulations and leadership skills are essential for success in this position.
What are some of the main challenges faced by a Manager Pharmacovigilance, and how can they be addressed?
A Manager Pharmacovigilance often navigates challenges such as staying current with evolving global regulatory requirements, managing large volumes of safety data, and ensuring timely and accurate adverse event reporting. Proactively implementing streamlined workflows, regular team training, and leveraging robust safety databases can help manage these demands efficiently. Collaboration with cross-functional teams, regulatory authorities, and external partners is essential for addressing complex cases and ensuring compliance. Being adaptable and detail-oriented also helps managers prioritize tasks and respond effectively to urgent safety concerns.
What are the key skills and qualifications needed to thrive in the Manager Pharmacovigilance position, and why are they important?
To thrive as a Manager Pharmacovigilance, you need a strong background in pharmaceutical sciences, drug safety regulations, and pharmacovigilance processes, often supported by a degree in pharmacy, life sciences, or medicine. Familiarity with pharmacovigilance databases (such as Argus Safety or ArisGlobal), regulatory reporting tools, and industry-standard certifications like Drug Safety or Pharmacovigilance certifications is highly valued. Excellent leadership, communication, and cross-functional collaboration skills set top candidates apart. These competencies are crucial to ensure compliance, manage risk, and lead teams effectively in monitoring and improving drug safety throughout a product's lifecycle.
- Pharmacovigilance Manager Salary
- Full Time Pharmacovigilance
- Weekend Pharmacovigilance
- Pharmacovigilance Operations
- Global Pharmacovigilance
- Temporary Drug Safety Pharmacovigilance
- Remote Pharmacovigilance Associate
- Pharmacovigilance Recruiters
- Remote Online Pharmacovigilance
- Senior Manager Pharmacovigilance

Full-time
Medical, Dental, Vision, Life, Retirement
Posted 10 days ago
AssistRx rating
7.2
Based on 20 frontline employees who took The Breakroom Quiz
134th of 221 rated it services
Job description
The Manager, Pharmacovigilance - Front End Operations will lead frontline operational support for pharmacovigilance (PV) activities, directly interfacing with Quality Assurance, Patient Solutions, and Compliance to ensure consistent alignment with global regulatory requirements for drug safety, reporting, and risk management. This role is instrumental in establishing and maintaining frameworks for audit readiness, proactive monitoring, and continuous improvement, and in promoting a cohesive approach across Quality Assurance and patient-facing teams to uphold safety standards and regulatory compliance.
- Drive the execution of PV compliance activities to meet global regulatory requirements (DEA, State Board of Pharmacy, URAC and ACHC, OIG, etc.) and industry standards, with a focus on operational integration with Quality Assurance and Patient Solutions.
- Partner closely with Quality Assurance and Operations to develop, implement, and manage PV compliance frameworks, including SOPs, processes, and systems for program drug safety reporting.
- Work directly with cross-functional teams, including Patient Solutions, Pharmacy, Regulatory Affairs, and Clinical, to facilitate an integrated and patient-centered approach to PV compliance.
- Ensure PV systems are audit-ready, including preparing for and supporting regulatory authority inspections.
- Conduct regular assessments of PV risk management, identify and address compliance gaps, and recommend improvements in collaboration with QA and Patient Solutions.
- Monitor regulatory changes in PV and assess their impact on front-end operations, keeping stakeholders informed of updates and required actions.
- Oversee and assess quality performance of internal and external resources, regularly reporting to senior management.
- Support internal and external PV audits, including audits of business partners and service providers, ensuring findings are communicated and addressed.
- Contribute to the development and delivery of PV compliance training tailored to frontline and patient solutions teams.
- Facilitate the timely preparation and submission of regulatory filings related to PV, including safety reports and risk management plans.
- Assist in investigations of compliance breaches, implementing corrective and preventive actions (CAPAs) as needed.
- Actively engage in continuous improvement initiatives to enhance PV processes and ensure quality integration across all frontline operations.
- Performs other related duties as assigned by management.
- Carries out supervisory responsibilities in accordance with the organization's policies and applicable laws.
- Responsibilities include interviewing; hiring; training; coaching/mentoring; planning, assigning, and directing work; appraising performance; professional development; disciplinary actions; addressing complaints; and resolving problems.
Requirements
- Education: Bachelor's degree in a scientific discipline (Pharmacy, Life Sciences, etc.) or equivalent experience required.
- 7+ years of experience in pharmacovigilance/drug safety, with 3+ years in a compliance, oversight, or quality-driven role.
- Strong knowledge of global PV regulations, including ICH guidelines and GVP Modules.
- Experience with health authority inspections (e.g., DEA, State Board of Pharmacy, URAC and ACHC, OIG, etc.) and audit readiness.
- Experience in biopharmaceutical or biotechnology industries preferred
- Certification in pharmacovigilance, compliance, or related fields preferred
- Familiarity with PV databases and safety signal detection tools preferred
- Experience working with cross-functional teams, including patient-facing teams, with proven skills in stakeholder management.
- Proficiency in quality reporting tools and establishing performance metrics.
- Experience drafting and developing procedural documents and training programs.
- Strong organizational and leadership skills with a focus on front-end and patient-centered operations.
- Excellent collaboration and engagement skills, with the ability to drive cross-functional teamwork.
- Proven project management and problem-solving abilities.
- Detail-oriented, analytical, and capable of managing complex requirements in a fast-paced environment.
- Strong written and verbal communication skills.
Benefits
- Supportive, progressive, fast-paced environment
- Competitive pay structure
- Matching 401(k) with immediate vesting
- Medical, dental, vision, life, & short-term disability insurance
Wondering how we recognize our employees for delivering best in class results? Here are some of the awards that our employees receive throughout the year!
- #TransformingLives Honor: This quarterly award program is a peer to peer honor that recognizes and highlights some of the amazing ways that our team members are transforming lives for patients on a daily basis.
- Values Award: This quarterly award program recognizes individuals who exhibit one, or many, of our core company values; Excellence, Winning, Respect, Inspiration, and Teamwork.
- Vision Award: This annual award program recognizes an individual who has gone above and beyond to support the AssistRx vision to transform lives through access to therapy.
AssistRx, Inc. is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, religion, color, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, family medical history or genetic information, political affiliation, military service, or other non-merit based factors, or any other protected categories protected by federal, state, or local laws.
All offers of employment with AssistRx are conditional based on the successful completion of a pre-employment background check.
In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire. Sponsorship and/or work authorization is not available for this position.
AssistRx does not accept unsolicited resumes from search firms or any other vendor services. Any unsolicited resumes will be considered property of AssistRx and no fee will be paid in the event of a hire.
About AssistRx
Sourced by ZipRecruiter
Industry
It services
Company size
51 - 200 Employees
Headquarters location
Orlando, FL, US
Year founded
2009