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New · posted Nov 1

Thermo Fisher Scientific · Pharmaceuticals

Associate Director, Pharmacovigilance- FSP

  • Chapel Hill, NC
  • On-site
  • Full-time
  • Director
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DeadlineOpen until filled

The role

Join Us as a Associate Director, PV

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

The Associate Director, PVG ensures the delivery of safety management services consistent with company SOPs/WPDs, ICH guidelines and regulatory requirements. Works with managers and liaises with other departmental personnel as required. Oversees function operations and manages the activities of managers and other staff. Develops and maintains departmental SOPs/WPDs, and long-range planning for new processes and staffing needs. Prepares business proposals and client presentations and interacts frequently with members of the Business Development and Bids and Contracts groups.

What you need

Education and Experience Requirements

  • Bachelor's degree or equivalent and relevant formal academic / vocational qualification.
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 10+ years).
  • 5+ years of management responsibility
  • Proven leadership skills

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills, Abilities

  • Expertise in global regulatory requirements for adverse event reporting, ICH safety guidelines, GCP etc.
  • Knowledgeable of safety database management
  • Expertise in budgeting, forecasting and fiscal management
  • Analytical skills as well as excellence in oral and written communications
  • Ability to handle multiple issues on multiple projects simultaneously
  • Know how to maintain a high degree of independence with respect to decision making and problem solving
  • Ability to act as liaison with other divisions necessary to complete contract/regulatory requirements
  • Strong negotiating skills
  • Ability to analyze and evaluate processes and procedures

What you'll do

  • Oversee effectiveness of department operations to include safety processes, resource utilization, scope of work, budget and contractual issues
  • Develop processes and strategies designed to assist in meeting departmental and company goals.
  • Oversee compliance with all relevant company policies, procedures and global regulations.
  • Guide managers and train project team members as appropriate.
  • Assist business development and foster client relationships and provide department business development presentations for clients to help secure new business as well as retain ongoing business for existing clients.
  • Review and provide operational input on budgets, proposals, contracts and/or renewals associated with existing clients.
  • Manage staff of experienced professionals, which may include interviewing and selection, job description preparation, professional development, goal setting, performance management, coaching and mentoring, employee counseling, and separations. Approve courses of action on salary administration, hiring, corrective action, and terminations. Review and approve time records, expense reports, requests for leave, and overtime.

Where you'll work

Chapel Hill, NCOn-siteOpen in Maps (opens in a new tab)

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Schedule and working conditions

Days

Shift5 days a week

Standard (Mon-Fri)

Environmental Conditions

Office

Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive.

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

Job intelligence

The context around this role

Live data · November 1, 2026

Salary intelligence

How the pay compares

Director roles in the US90 roles publishing pay

Middle half $218,875 to $281,000, median $264,000
Annual base pay
Annual base payLowMedianHigh
All US$218,875$264,000$281,000

Comparisons: the base pay employers published on open Clinical Safety & Pharmacovigilance roles at the same level on Regulatory Jobs, November 1, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Safety & Pharmacovigilance

The general path across 162 open Clinical Safety & Pharmacovigilance roles on Regulatory Jobs, with the titles they carry most. Not Thermo Fisher's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: Associate, Pharmacovigilance Operations/Drug Safety · Clinical Safety Coordinator

    $92K median10 open
  2. Earlier

    Senior & Principal

    Often: Senior Safety Scientist · Clinical FSP Quality Manager

    $172K median17 open
  3. One step back

    Manager

    Often: Senior Manager, Clinical Quality Assurance · Clinical FSP Quality Manager

    $166K median30 open
  4. This role

    Director

    Often: Director · Senior Medical Director

    $264K median92 open
  5. Next step

    VP & Executive

    Often: Head of Multiple Myeloma & AML, Oncology · Head of Patient-Facing Quality Assurance

    $347K median13 open

Skills DNA

What this role leans on

How many of the posting's 25 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 2 linesLab testing and methods: 2 linesDocumentation and SOPs: 4 linesValidation and qualification: 1 lineClinical trial conduct: 3 linesCollaboration and leadership: 7 linesGMPLab testingDocumentationValidationClinical trialsTeamwork
  • Collaboration and leadership7
  • Documentation and SOPs4
  • Clinical trial conduct3
  • GMP and compliance2
  • Lab testing and methods2
  • Validation and qualification1

Company hiring pulse

Thermo Fisher on Regulatory Jobs

119
Open roles
106
Distinct roles
52
Locations

By discipline

  • Quality77 65%
  • Clinical36 30%
  • Regulatory6 5%

By level

  • Senior & Principal51 43%
  • Associate & Specialist35 29%
  • Manager27 23%
See all 119 Thermo Fisher roles

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Associate Director, Pharmacovigilance- FSP at Thermo Fisher

Open until filled.

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