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Pharmacovigilance Trainee Jobs (NOW HIRING)

Loyola University Chicago

Staff Scientist

Chicago, IL · On-site

Trainees who join Dr. Sodhi's Lab will gain experience in Molecular Genetics, Gene expression studies of rodent or human tissue, behavioral Pharmacology, mammalian cell culture, in addition to ...

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How much do pharmacovigilance trainee jobs pay per year?

As of Aug 16, 2026, the average yearly pay for pharmacovigilance trainee in the United States is $89,898.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,000.00 and $119,000.00 per year, depending on experience, location, and employer.

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

To thrive as a Pharmacovigilance Trainee, you need a solid background in life sciences or pharmacy, strong analytical skills, and attention to detail, often supported by a relevant degree. Familiarity with safety databases like Argus or ARISg, as well as knowledge of regulatory guidelines such as ICH-GCP, is commonly required. Excellent communication, critical thinking, and the ability to work collaboratively make an individual stand out in this role. These skills are crucial for ensuring accurate adverse event reporting, regulatory compliance, and maintaining patient safety in the pharmaceutical industry.

What is the difference between Pharmacovigilance Trainee vs Pharmacovigilance Associate?

AspectPharmacovigilance TraineePharmacovigilance Associate
Required CredentialsTypically pursuing or recently completed relevant degree (e.g., pharmacy, life sciences)Bachelor's degree in life sciences or related field; certification preferred
Work EnvironmentTraining programs, supervised tasks, entry-level rolesFull-time, independent handling of PV activities
Employer & Industry UsageInternships, training programs in pharma/biotech companiesEstablished roles in pharmaceutical companies and CROs
Comparison Search IntentYesYes

In summary, Pharmacovigilance Trainees are usually students or recent graduates undergoing training, focusing on learning PV processes. Pharmacovigilance Associates are more experienced, handling PV tasks independently. Both roles are essential in the drug safety industry but differ mainly in experience and responsibilities.

What is a pharmacovigilance trainee?

A Pharmacovigilance Trainee is an entry-level professional who assists in monitoring, assessing, and reporting the safety of pharmaceutical products. Their main responsibilities include collecting and evaluating information on adverse drug reactions, preparing safety reports, and ensuring compliance with regulatory guidelines. This role is essential to ensure the ongoing safety and efficacy of medicines after they reach the market. Trainees work under the supervision of experienced pharmacovigilance professionals and often receive training on regulatory requirements and safety data management.

What are the typical responsibilities of a pharmacovigilance trainee?

As a Pharmacovigilance Trainee, you will be involved in collecting, processing, and evaluating reports of adverse drug reactions (ADRs) from healthcare professionals and patients. Your responsibilities may include entering case data into safety databases, performing literature searches for safety-related information, and assisting with the preparation of regulatory reports and periodic safety update reports (PSURs). You will work closely with experienced pharmacovigilance professionals and cross-functional teams such as medical affairs and regulatory affairs, gaining exposure to the end-to-end safety monitoring process. This foundational experience is essential for understanding compliance requirements and the critical role pharmacovigilance plays in patient safety.
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Pharmacovigilance Trainee jobs near you
Infographic showing various Pharmacovigilance Trainee job openings in the United States as of August 2026, with employment types broken down into 91% Full Time, and 9% Part Time. Highlights an 100% In-person job distribution, with an average salary of $89,898 per year, or $43.2 per hour.

Postdoctoral Associate , Human Intestinal Models and Oral Delivery Modeling

System One

Pittsburgh, PA • On-site

Full-time

Re-posted 25 days ago

Job description

Job Title: Postdoctoral Associate, Human Intestinal Models and Oral Delivery Modeling Location: Onsite, Pittsburgh, PA 15213 Type: Direct-Hire/Permanent Hours: Standard business hours Start: May Overview: We are looking for a highly motivated Postdoctoral Associate to join a lab focused on discovering novel therapeutics. This interdisciplinary program develops advanced in vitro models of hematopoietic and immune system function such as conducting research at the intersection of microphysiological systems (Organs-on-Chips) and immunology. The role emphasizes the use of intestine-based and interconnected microphysiological systems to model oral delivery, absorption, and systemic distribution of therapeutic agents under physiologically relevant conditions, with integration into multi-organ platforms to enable pharmacokinetic and pharmacodynamic (PK/PD) analyses. Responsibilities:

  • Establish and maintain intestine-based Organs-on-Chips using primary or relevant epithelial cell systems
  • Design and execute studies evaluating oral delivery, absorption, and transport of therapeutic agents under controlled experimental conditions
  • Perform and optimize assays to assess epithelial barrier function, transport dynamics, and tissue responses
  • Support multi-organ integration studies to enable PK/PD analyses across interconnected in vitro systems
  • Contribute to development and refinement of experimental workflows to enhance reproducibility and physiological relevance
  • Collaborate with multidisciplinary teams to integrate intestinal data with complementary organ systems and analytical platforms
  • Support data generation, analysis, and interpretation, including integration of findings across studies
  • Maintain accurate and detailed documentation of experimental procedures and results
  • Contribute to preparation of manuscripts, reports, and grant applications
  • Mentor trainees and assist in training of laboratory personnel as needed

Requirements:

  • Ph.D. in Pharmacology, Biomedical Engineering, Physiology, or a related field
  • Experience with human intestinal cells and models, and/or intestinal transport biology
  • Strong background in experimental design and quantitative analysis
  • Strong analytical, organizational, and problem-solving skills
  • Ability to work independently and collaboratively in a multidisciplinary research environment
  • Strong written and verbal communication skills
Preferred:
  • Experience with intestinal models, barrier function assays, or drug absorption studies
  • Familiarity with pharmacokinetic/pharmacodynamic (PK/PD) concepts
  • Experience with Organs-on-Chips or integrated tissue models
  • Experience working in interdisciplinary teams integrating biology, engineering, and pharmacology

#M3 Ref: #558-Scientific