ZipRecruiter

Log In

1

Pharmacovigilance Associate Jobs in Delaware (NOW HIRING)

QPS, LLC

Associate Scientist I - TLM

Newark, DE · On-site

$45K - $50K/yr

  • Life

  • Retirement

... Immunology, Pharmacology, Medical Technology, or a related field as follows: * Bachelor's Degree * Associate's Degree plus 2 or more years relevant experience * Desire to learn and grow ...

Serco

Medical Coding Auditing Specialist 1 1

Dover, DE · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Education: * An associate's degree or higher in Health Information Management or Healthcare ... pharmacology; OR * Successful completion of an American Academy of Professional Coders (AAPC) or ...

Nemours

Clinical Pharmacist (Midnight Shift)

Wilmington, DE · On-site

$115K - $137K/yr

... pharmacokinetic variations in drug absorption, distribution, metabolism, and elimination with ... Associates who are not licensed in the state of DE at time of hire must start process for licensure ...

All JobsPharmacovigilance Associate JobsPharmacovigilance Associate Jobs in Delaware

Pharmacovigilance Associate information

See Delaware salary details

$12

$49

$85

How much do pharmacovigilance associate jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for pharmacovigilance associate in Delaware is $49.19, according to ZipRecruiter salary data. Most workers in this role earn between $38.51 and $55.58 per hour, depending on experience, location, and employer.

What is a pharmacovigilance associate?

A Pharmacovigilance Associate is responsible for monitoring, collecting, assessing, and reporting adverse drug reactions (ADRs) to ensure patient safety. They work with regulatory authorities, healthcare professionals, and pharmaceutical companies to analyze drug safety data. Their duties include case processing, literature screening, signal detection, and ensuring compliance with pharmacovigilance regulations. This role is vital for minimizing drug-related risks and maintaining regulatory compliance.

What are the typical daily responsibilities of a pharmacovigilance associate?

A Pharmacovigilance Associate is responsible for collecting, reviewing, and processing reports of adverse drug reactions, ensuring that all data is accurate and submitted in accordance with regulatory timelines. On a daily basis, you may enter case information into specialized safety databases, conduct follow-ups with healthcare professionals or patients for additional details, and assist in preparing safety reports for regulatory authorities. The role often involves close collaboration with medical, regulatory, and quality assurance teams to support comprehensive drug safety monitoring. You may also participate in ongoing training or audits to maintain compliance with evolving industry standards.

What are the key skills and qualifications needed to thrive as a pharmacovigilance associate?

To thrive as a Pharmacovigilance Associate, you need a strong background in life sciences or pharmacy, attention to detail, and a solid understanding of drug safety regulations. Familiarity with safety databases such as Argus or ARISg, as well as knowledge of global regulatory guidelines like FDA and EMA requirements, is often required. Strong analytical thinking, effective communication, and organizational skills help you manage case reports and collaborate with cross-functional teams. These skills are essential for accurately assessing and reporting adverse drug reactions to ensure patient safety and regulatory compliance.

Is pharmacovigilance a good career path?

Pharmacovigilance is a growing field that involves monitoring the safety of pharmaceutical products, with roles like Pharmacovigilance Associate focusing on adverse event reporting and data analysis. It offers opportunities for career advancement, requires attention to detail, and often involves working with regulatory guidelines and safety databases. Many professionals find it a stable and rewarding career in the healthcare and pharmaceutical industries.

What qualifications do I need for pharmacovigilance?

A pharmacovigilance associate typically needs 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 case management tools; certifications such as the Drug Safety Certification (DSC) can also be beneficial.

What are the most commonly searched types of Pharmacovigilance jobs in Delaware?

The most popular types of Pharmacovigilance jobs in Delaware are:

What are popular job titles related to Pharmacovigilance Associate jobs in Delaware?

For Pharmacovigilance Associate jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Pharmacovigilance Associate jobs in Delaware look for?

The top searched job categories for Pharmacovigilance Associate jobs in Delaware are:

What cities in Delaware are hiring for Pharmacovigilance Associate jobs?

Cities in Delaware with the most Pharmacovigilance Associate job openings:

Pharmacovigilance Associate jobs near you
Infographic showing various Pharmacovigilance Associate job openings in Delaware as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $102,305 per year, or $49.2 per hour.

Associate Director, Quantitative Pharmacology

Incyte Corporation

Wilmington, DE • On-site

Full-time

Re-posted 25 days ago

Job description

Overview
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity
Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
Job Summary (Primary function)
We are seeking a pharmacometrician to join our Clinical and Quantitative Pharmacology organization in Translational Medicine. An Associate Director is responsible for executing on the pharmacometrics strategy and model-based analyses for clinical drug development and is expected to play a key role in supporting programs. This role will be responsible for developing and implementing model-informed drug development (MIDD) strategies to optimize decision-making across all phases of drug development.
Essential Functions of the Job (Key responsibilities)
  • Responsible for independently conducting and reporting model-based analyses including population pharmacokinetics (PK) and pharmacokinetics/pharmacodynamics (PK/PD), exposure-response modeling, model-based meta-analyses (MBMA), disease progression modeling, and clinical trial simulation.
  • Identifies opportunities where modeling and simulation can advance the understanding of pharmacokinetics, pharmacodynamics, efficacy, and safety across multiple projects
  • Accountable for developing MIDD strategies across multiple programs and disease areas to optimize prospective studies, inform the overall clinical development and regulatory strategies in collaboration with partners (clinical pharmacology, biostatistics, regulatory, and clinical development teams)
  • Effectively communicates results, conclusions, and assumptions of pharmacometrics analyses to a variety of audiences to influence the decision-making process (written and oral presentation)
  • Mentors and guides peers in pharmacometrics methodologies, tools, and their application in clinical drug development
  • Stays current with scientific advancements and regulatory trends in clinical pharmacology and pharmacometrics, and applies the knowledge to advance drug development for the organization
  • Publishes in peer-reviewed journals

Qualifications (Minimal acceptable level of education, work experience, and competency)
  • Ph.D. in Pharmacometrics, Clinical Pharmacology, Applied Mathematics, Statistics, Engineering, or a related field.
  • Demonstrated 3-5 years of related industry experience.
  • Hands-on experience in a statistical programming language and pharmacometrics analysis software including R and NONMEM or equivalents
  • Excellent communication skills and ability to collaborate with cross-functional teams
  • Time management and ability to balance execution of multiple tasks to accomplish program goals.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
We Respect Your Privacy
Learn more at: http://www.incyte.com/privacy-policy
The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.
During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here.
You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.
You can learn more about Incyte's data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte's data protection officer, and your supervisory authority (if applicable).
Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.

Apply