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Entry Level Pharmacovigilance Associate Jobs (NOW HIRING)

City of New York

CHEMIST 2

Queens, NY · On-site

$23.25 - $31/hr

BEDC seeks to hire an Associate Chemist 2 for the Engineering Services, Laboratory Services Section ... pharmacology, toxicology, environmental science, forensic science, or other natural science.

City of New York

CHEMIST 2

Queens, NY · On-site

$23.25 - $31/hr

BEDC seeks to hire an Associate Chemist 2 for the Engineering Services, Laboratory Services Section ... pharmacology, toxicology, environmental science, forensic science, or other natural science.

Tigermed America

Be Seen First

Clinical Research Associate

Denver, CO · Remote

Provide guidance and training to entry-level CRA/CRA I/CRA II in collaboration with Line Manager. 3. Qualifications: * Bachelor degree or above in Medical, Pharmacology or Biology related major;

Tigermed America

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Clinical Research Associate

Denver, CO · Remote

Provide guidance and training to entry-level CRA/CRA I/CRA II in collaboration with Line Manager. 3. Qualifications: * Bachelor degree or above in Medical, Pharmacology or Biology related major;

Citizens Medical Center

Physician Coder (FT)

Victoria, TX · On-site

$17.50 - $23.25/hr

Associates degree in a healthcare related field; Knowledge of pathophysiology and basic pharmacology; Entry level knowledge of health insurance (HMO, PPO, Medicare, Medicaid, etc.) EXPERIENCE ...

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Entry Level Pharmacovigilance Associate information

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$12

$49

$85

How much do entry level pharmacovigilance associate jobs pay per hour?

As of Jul 4, 2026, the average hourly pay for entry level pharmacovigilance associate in the United States is $49.14, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $55.53 per hour, depending on experience, location, and employer.

What are some typical challenges faced by Entry Level Pharmacovigilance Associates when handling case processing?

Entry Level Pharmacovigilance Associates often encounter challenges such as managing high volumes of adverse event reports, ensuring data accuracy, and meeting strict regulatory timelines. It can be demanding to quickly learn and apply complex medical terminology and global reporting regulations. Collaboration with cross-functional teams, such as clinical research and regulatory affairs, is essential for clarifying information and ensuring proper documentation. Over time, you’ll develop strong analytical and communication skills, which are valuable for advancing within the field.

What are the key skills and qualifications needed to thrive as an Entry Level Pharmacovigilance Associate, and why are they important?

To thrive as an Entry Level Pharmacovigilance Associate, you need a foundational knowledge of life sciences, attention to detail, and often a bachelor’s degree in pharmacy, medicine, or a related field. Familiarity with pharmacovigilance databases (such as Argus Safety or ARISg), MedDRA coding, and regulatory guidelines is typically required. Strong analytical thinking, effective communication, and organizational skills help you excel in processing and reporting safety data. These abilities are vital to ensure accurate adverse event reporting and compliance with regulatory standards, directly impacting patient safety.

What is the difference between Entry Level Pharmacovigilance Associate vs Entry Level Drug Safety Associate?

AspectEntry Level Pharmacovigilance AssociateEntry Level Drug Safety Associate
Required CredentialsBachelor's degree, relevant certifications (e.g., PV training)Bachelor's degree, often similar certifications
Work EnvironmentPharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, biotech firms
Industry UsageCommonly used in pharmacovigilance and drug safety departmentsOften used interchangeably, focusing on drug safety tasks

Both roles involve monitoring drug safety and require similar educational backgrounds and certifications. The main difference lies in terminology preference; 'Pharmacovigilance Associate' emphasizes the safety monitoring process, while 'Drug Safety Associate' is a broader term used interchangeably in the industry. Both positions are entry-level roles in the pharmaceutical and biotech sectors focused on ensuring medication safety.

What does an Entry Level Pharmacovigilance Associate do?

An Entry Level Pharmacovigilance Associate is responsible for supporting the collection, assessment, and reporting of adverse drug reactions and other safety-related information in the pharmaceutical industry. They help ensure that potential risks associated with medications are identified and communicated to regulatory authorities in compliance with legal requirements. Typical duties include data entry, case processing, literature screening, and assisting with regulatory submissions. This role is essential for maintaining patient safety and drug efficacy throughout a product's lifecycle.
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Entry Level Pharmacovigilance Associate jobs near you
Associate Scientist - Biochemistry

Associate Scientist - Biochemistry

Eurofins

Lancaster, PA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago

Eurofins rating

7.4

Company rating: 7.4 out of 10

Based on 179 frontline employees who took The Breakroom Quiz

57th of 103 rated laboratories

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.
Job Description
A perfect entry level opportunity!
  • Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, devices, aerosols, liquids, creams, and gels)
  • Run the instrumentation independently including, but not limited to, various chromatographic systems
  • Preparing samples for analysis and running some instrumentation with minimum supervision
  • Set up and validate new analytical or related processes used by the department
  • Prepare standards and samples for analysis
  • Execute method transfer protocols
  • Document work as required for GMP compliance
  • Perform monthly maintenance of laboratory equipment

Qualifications
Qualifications:
  • Strong computer, scientific, and organizational skills
  • Excellent communication (oral and written) and attention to detail
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies

Minimum Qualifications:
  • Bachelor's degree in chemistry or other related degree concentration, or equivalent directly-related experience
  • Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information
Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with overtime as needed. Candidates currently living within a commutable distance of Lancaster, Pennsylvania are encouraged to apply.
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 BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

What Eurofins employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

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About Eurofins

Sourced by ZipRecruiter

Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US

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