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Pv Scientist Jobs in Raleigh, NC (NOW HIRING)

GSK

SERM Scientific Director

Durham, NC · On-site

Key Responsibilities Scientific/Medical Knowledge PV Expertise * Leads Pharmacovigilance and Risk Management Planning and develops strategy for approach to evaluation of issues in the clinical matrix.

GlaxoSmithKline

SERM Scientific Director

Durham, NC

Key Responsibilities Scientific/Medical Knowledge PV Expertise * Leads Pharmacovigilance and Risk Management Planning and develops strategy for approach to evaluation of issues in the clinical matrix.

AECOM

Electrical Engineer (BESS Focus)

Raleigh, NC · On-site +1

... scientists, digital innovators, program and construction managers and other professionals ... Solar PV and BESS system energy production modelling * Developing construction and equipment ...

AECOM

Electrical Engineer (BESS Focus)

Raleigh, NC · On-site +1

... scientists, digital innovators, program and construction managers and other professionals ... Solar PV and BESS system energy production modelling * Developing construction and equipment ...

AECOM

Electrical Engineer (BESS Focus)

Raleigh, NC · On-site +1

... scientists, digital innovators, program and construction managers and other professionals ... Solar PV and BESS system energy production modelling * Developing construction and equipment ...

AECOM

Electrical Engineer (BESS Focus)

Raleigh, NC · On-site +1

... scientists, digital innovators, program and construction managers and other professionals ... Solar PV and BESS system energy production modelling * Developing construction and equipment ...

AECOM

Electrical Engineer (BESS Focus)

Raleigh, NC · On-site

... scientists, digital innovators, program and construction managers and other professionals ... Solar PV and BESS system energy production modelling * Developing construction and equipment ...

AECOM

Electrical Engineer (BESS Focus)

Raleigh, NC · On-site +1

... scientists, digital innovators, program and construction managers and other professionals ... Solar PV and BESS system energy production modelling * Developing construction and equipment ...

AECOM

Electrical Engineer (BESS Focus)

Raleigh, NC · On-site +1

... scientists, digital innovators, program and construction managers and other professionals ... Solar PV and BESS system energy production modelling * Developing construction and equipment ...

AECOM

Electrical Engineer (BESS Focus)

Raleigh, NC · On-site +1

... scientists, digital innovators, program and construction managers and other professionals ... Solar PV and BESS system energy production modelling * Developing construction and equipment ...

AECOM

Electrical Engineer (BESS Focus)

Raleigh, NC · On-site +1

... scientists, digital innovators, program and construction managers and other professionals ... Solar PV and BESS system energy production modelling * Developing construction and equipment ...

AECOM

Electrical Engineer (BESS Focus)

Raleigh, NC · On-site +1

... scientists, digital innovators, program and construction managers and other professionals ... Solar PV and BESS system energy production modelling * Developing construction and equipment ...

AECOM

Electrical Engineer (BESS Focus)

Raleigh, NC · On-site +1

... scientists, digital innovators, program and construction managers and other professionals ... Solar PV and BESS system energy production modelling * Developing construction and equipment ...

AECOM

Electrical Engineer (BESS Focus)

Raleigh, NC · On-site +1

... scientists, digital innovators, program and construction managers and other professionals ... Solar PV and BESS system energy production modelling * Developing construction and equipment ...

AECOM

Electrical Engineer (BESS Focus)

Raleigh, NC · On-site +1

... scientists, digital innovators, program and construction managers and other professionals ... Solar PV and BESS system energy production modelling * Developing construction and equipment ...

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Pv Scientist information

See Raleigh, NC salary details

$29

$59

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How much do pv scientist jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for pv scientist in Raleigh, NC is $59.70, according to ZipRecruiter salary data. Most workers in this role earn between $41.35 and $71.73 per hour, depending on experience, location, and employer.

What is a PV scientist?

A PV (Pharmacovigilance) Scientist is responsible for monitoring, assessing, and preventing adverse drug reactions to ensure patient safety. They analyze safety data, contribute to risk management plans, and prepare regulatory reports. PV Scientists collaborate with medical, regulatory, and clinical teams to ensure compliance with global safety regulations. Their role is critical in ensuring drug safety throughout a product’s lifecycle.

What does a PV scientist do?

A typical day for a PV Scientist involves reviewing and analyzing individual case safety reports, assessing potential safety signals, and preparing regulatory safety documents and risk management plans. You may participate in team meetings with cross-functional partners such as clinical, regulatory, and medical affairs teams to discuss ongoing safety concerns or emerging issues. Additionally, you’ll interact with global health authorities, respond to their inquiries, and ensure compliance with evolving drug safety regulations. The work is detail-oriented and deadline-driven, but it also offers valuable opportunities for professional growth and meaningful contributions to patient safety.

What are the key skills and qualifications needed to thrive as a PV scientist?

To thrive as a PV (Pharmacovigilance) Scientist, you need an academic background in life sciences or pharmacy, in-depth knowledge of drug safety regulations, and strong analytical skills. Familiarity with pharmacovigilance databases (like Oracle Argus or ARISg), signal detection tools, and regulatory reporting systems is crucial, and certifications such as DSci or PV certifications are advantageous. Excellent written communication, critical thinking, and collaboration skills help you effectively interpret safety data and work cross-functionally. These competencies are essential for ensuring patient safety, regulatory compliance, and effective risk management in pharmaceutical environments.

What are popular job titles related to Pv Scientist jobs in Raleigh, NC?

For Pv Scientist jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Pv Scientist jobs in Raleigh, NC look for?

The top searched job categories for Pv Scientist jobs in Raleigh, NC are:

Pv Scientist jobs near you
Infographic showing various Pv Scientist job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 81% Full Time, 13% Part Time, and 4% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $124,179 per year, or $59.7 per hour.

Executive Medical Director, Psychiatry

Morrisville, NC • On-site, Remote

Thermo Fisher Scientific
Biotechnology Research and Development • 10K+ employees

7.8

Company rating: 7.8 out of 10

Based on 429 frontline employees who took The Breakroom Quiz

169th of 545 rated manufacturers

People enjoy working here

Good employer

Recommended by students

Learn more about Thermo Fisher Scientificexternal

Full-time

Posted 13 days ago

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
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.
Job Summary
The Executive Medical Director provides advanced medical and strategic leadership within the Pharmacovigilance (PV) physician organization. This role may include direct line management responsibilities and serves as a key liaison between PV physicians, PV leadership, cross-functional teams, and clients.
The Executive Medical Director provides leadership and strategic direction across pharmacovigilance, medical monitoring, quality and compliance, process improvement, training and development, business objectives, and innovation. The role applies therapeutic area and indication-specific expertise to provide medical consultation, guide benefit-risk evaluation and risk mitigation strategies, and support clinical development and business development activities.
This position may manage, mentor, and provide oversight to PV physicians globally, supporting end-to-end medical monitoring and safety physician activities throughout the pharmaceutical product lifecycle. The Executive Medical Director also contributes to resource planning, budget management, operational strategy, and continuous improvement initiatives.
Key Responsibilities
  • Provides global and regional medical leadership, mentoring, and oversight to PV physicians and, where applicable, direct reports.
  • Serves as a senior medical and pharmacovigilance subject matter expert and represents the PV physician organization on significant internal and external matters.
  • Applies clinical, therapeutic area, and pharmacovigilance expertise to the interpretation of safety and efficacy data, benefit-risk evaluation, safety signal assessment, risk mitigation, and clinical trial data interpretation.
  • Provides strategic medical oversight of clinical trial serious adverse events, aggregate safety data, individual case safety reports, periodic safety reports, signal detection activities, risk management plans, labeling activities, and other client deliverables.
  • Establishes relationships with key decision-makers and collaborates with cross-functional leaders on strategic initiatives, process improvements, and training and development programs.
  • Provides leadership on quality and regulatory compliance matters and serves as a subject matter expert during audits and inspections.
  • Identifies significant medical monitoring and safety issues and develops appropriate prevention, mitigation, and corrective strategies.
  • Supports business development activities, including strategy discussions, proposal development, bid reviews, and development of parameters for business deliverables.
  • Provides global leadership for medical safety and risk mitigation activities and develops strong client relationships.
  • Provides medical expertise and oversight for study start-up activities and medical deliverables.
  • Partners with sponsors to obtain direction and feedback regarding program scope, deliverables, and performance.
  • Participates in recruitment and selection activities.
  • Where applicable, manages employee onboarding, performance management, compensation administration, development, promotion, employee relations, and conflict resolution.
  • Develops and manages resource allocation plans and budgets.
  • Maintains an understanding of contracts, budgets, project time allocation, and related operational requirements.
  • Builds a collaborative, accountable, and high-performing team environment focused on quality, delivery, and continuous improvement.

Education and Experience
  • MD or equivalent medical degree required.
  • History of an active medical license highly preferred.
  • Typically requires 12+ years of relevant professional experience providing the knowledge, skills, and abilities necessary to perform the role.
  • Minimum of 2 years of clinical experience treating patients as a psychiatrist with direct responsibility for diagnostic and treatment decisions.
  • Minimum of 5 years of clinical trial experience within a CRO, pharmaceutical company, or as an industry principal investigator.

An equivalent combination of appropriate education, training, and directly related experience may be considered.
Knowledge, Skills, and Abilities
  • Deep therapeutic and indication-specific drug development expertise across one or more therapeutic areas and/or drug classes.
  • Strong knowledge of clinical development programs, study design, endpoints, safety considerations, and the regulatory and commercial landscape.
  • Deep understanding of regulatory requirements governing adverse event reporting and experience working with the FDA, EMA, and other national and international regulatory authorities.
  • Demonstrated experience providing medical strategy leadership to multidisciplinary teams.
  • Extensive knowledge of medical monitoring, including adverse event review, protocol inquiries, listings, diagnostic reports, data trending, and related activities.
  • Strong knowledge of pharmacovigilance activities, including signal detection, aggregate reporting, labeling updates, dossier maintenance, and risk management.
  • Thorough understanding of marketing authorization submission requirements and international clinical study guidelines.
  • Strong decision-making, negotiation, analytical, communication, and influencing skills.
  • Demonstrated ability to lead, mentor, develop, and objectively evaluate medical professionals.
  • Excellent organizational skills with a detail-oriented leadership approach.
  • Strong knowledge of the overall drug development lifecycle.
  • Ability to work independently, manage multiple priorities, and operate effectively in a fast-paced global environment.
  • Ability to travel domestically and internationally as required.

Working Conditions and Environment:
  • Work is performed in an office environment with exposure to electrical office equipment.
  • Occasional driving to site locations and occasional domestic and international travel.

Physical Requirements:
  • Frequently stationary for 6-8 hours per day.
  • Repetitive hand movements, including the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
  • Frequent mobility required.
  • Occasional crouching, stooping, bending, and twisting of the upper body and neck.
  • Light to moderate lifting and carrying of objects, including luggage and laptop computers, up to 15-20 lbs.
  • Ability to access and use a variety of computer software, including both internally developed and commercially available applications.
  • Ability to communicate information and ideas clearly and to understand information presented through spoken words and sentences.
  • Frequent interaction with diverse groups to obtain and communicate information.
  • Ability to work independently with minimal guidance, plan work schedules to meet goals, and maintain concentration for extended periods.
  • Ability to perform a wide range of tasks in response to changing demands and conditions, manage multiple priorities, and perform effectively under pressure.
  • Regular and consistent attendance.

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