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Full Time Entry Level Pharmacovigilance Jobs (NOW HIRING)

... Pharmacokinetics) - Biologics Location: 760 Pennsylvania Dr, Exton, PA 19341 Full-time Frontage ... field. * Entry-level candidates, including recent graduates, are encouraged to apply. Hands-on ...

Entry Level Chemist

Lancaster, PA ยท On-site

$21.50 - $28.75/hr

... discovery pharmacology, forensics, advanced material sciences and in the support of clinical ... Excellent full time benefits including comprehensive medical coverage, dental, and vision options

Entry Level Chemist

Lancaster, PA

$21.50 - $28.75/hr

... discovery pharmacology, forensics, advanced material sciences and in the support of clinical ... Excellent full time benefits including comprehensive medical coverage, dental, and vision options

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Full Time Entry Level Pharmacovigilance information

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How much do full time entry level pharmacovigilance jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for full time entry level pharmacovigilance in the United States is $25.60, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $28.61 per hour, depending on experience, location, and employer.

What is a full time entry level pharmacovigilance professional?

A Full Time Entry Level Pharmacovigilance job involves monitoring, assessing, and reporting on the safety of pharmaceutical products to ensure they are safe for public use. Professionals in this role typically collect and analyze data on drug side effects and adverse events, help prepare regulatory reports, and support compliance with safety regulations. Entry-level positions often require a background in pharmacy, life sciences, or a related field, and provide training on pharmacovigilance processes and regulatory requirements. This is a great starting point for those interested in drug safety and regulatory affairs within the pharmaceutical industry.

What is the difference between Full Time Entry Level Pharmacovigilance vs Clinical Data Coordinator?

AspectFull Time Entry Level PharmacovigilanceClinical Data Coordinator
Required CredentialsBachelor's degree, basic pharmacovigilance trainingBachelor's degree, clinical data management training
Work EnvironmentPharmaceutical companies, CROs, regulatory agenciesClinical research sites, CROs, pharmaceutical companies
Industry UsageMonitoring drug safety, adverse event reportingManaging clinical trial data, data entry, quality checks
Common Search/ComparisonYesNo

Full Time Entry Level Pharmacovigilance roles focus on monitoring drug safety and adverse event reporting within the pharmaceutical industry, requiring basic pharmacovigilance training. Clinical Data Coordinators handle clinical trial data management, including data entry and quality checks. While both roles support clinical research, pharmacovigilance emphasizes safety monitoring, whereas data coordinators focus on data accuracy and integrity.

What are the key skills and qualifications needed to thrive as a full time entry level pharmacovigilance professional?

To thrive as a Full Time Entry Level Pharmacovigilance professional, you need a background in pharmacy, life sciences, or a related field, along with strong attention to detail and understanding of drug safety concepts. Familiarity with pharmacovigilance databases (such as Argus or ARISg), MedDRA coding, and basic regulatory guidelines is typically required. Strong analytical thinking, written communication, and the ability to work collaboratively make candidates stand out in this role. These skills are crucial for ensuring the accurate collection, assessment, and reporting of adverse drug events, which supports patient safety and regulatory compliance.

What are some common challenges faced by entry-level professionals in pharmacovigilance, and how can they be addressed?

Entry-level professionals in pharmacovigilance often encounter challenges such as learning complex regulatory requirements, adapting to detailed case processing, and managing high volumes of adverse event reports. To overcome these challenges, it's important to seek mentorship from experienced colleagues, participate in ongoing training sessions, and develop strong organizational skills. Building a solid understanding of standard operating procedures and staying updated with evolving global regulations can also help new hires excel in this critical field.
More about Full Time Entry Level Pharmacovigilance jobs
What cities are hiring for Full Time Entry Level Pharmacovigilance jobs? Cities with the most Full Time Entry Level Pharmacovigilance job openings:
What job categories do people searching Full Time Entry Level Pharmacovigilance jobs look for? The top searched job categories for Full Time Entry Level Pharmacovigilance jobs are:
Infographic showing various Full Time Entry Level Pharmacovigilance job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $53,254 per year, or $25.6 per hour.

Associate Scientist l (DNA) (Full-Time/Entry-Level)

Eurofins USA Genomic Services

River Falls, WI โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago


Job description

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

Pay Rate: $17.25/Hr.

Shift: Monday- Friday, 8:00am- 4:30 PM (Full-Time)

The GTS Department is dedicated to supporting ELISA/HB planting, harvesting, extraction, and testing; DNA QA grinding, plating, and testing; MBGT planting, plating and testing; Electrophoresis planting, plating, extraction and testing.

The GTS Department includes genetic purity testing using Isozyme Electrophoresis, trait purity testing using ELISA/Herbicide Bioassay testing, and adventitious presence and zygosity testing using in DNA QA using PCR.

The DNA Associate Scientist is responsible for helping in all activities, as directed, for the GTS/MBGT work streams, with primary focus in DNA extraction, testing, and data analysis.

Responsibilities and Duties

General:

  • Communicate effectively internally and externally
  • Work cooperatively
  • Participate in general laboratory maintenance
  • Effectively communicate sample/internal issues to Manager and/or Group Lead as appropriate
  • Effectively communicate personnel issues to Manager and/ or Group Lead

Specific:

  • Assist with the creation of plate maps for DNA QA
  • Assist in DNA QA extraction, testing, data analysis, and reporting
  • Become proficient in all areas of GTS planting/sample prep/evaluating/harvesting/extraction/testing
  • Help, support and maintain EBDI Safety program
  • Help, support and maintain EBDI ISO quality system
  • Ensure accurate and efficient execution of written protocols
  • Technical training on equipment/processes in different labs as needed
  • Other duties as needed
Qualifications

Education/Experience:

  • High school and science aptitude
  • Within a commutable distance of the worksite location. 
  • Authorization to work in the United States indefinitely without restriction or sponsorship

Skills:

  • Experience using Microsoft Office Suite

Other Factors:

  • Position requires sitting and standing for multiple hours, as well as lifting up to 50lbs. 

Additional Information

Shift: Monday- Friday, 8:00am- 4:30 PM (Full-Time)

What we offer:

  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

Eurofins USA Genomic Services is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins USA Genomic Services is a Disabled and Veteran Equal Employment Opportunity employer.