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Entry Level Pharmacovigilance Associate Jobs (NOW HIRING)

... discovery pharmacology, forensics, advanced material sciences and in the support of clinical ... The Quality Assurance Associate position is an entry-level position involved in day-to-day ...

Position Overview The Associate Clinic Research Nurse supports clinical research operations by ... Ensure pharmacokinetic rooms and clinical spaces are clean, stocked, and patient-ready. * Maintain ...

The Associate Clinic Research Nurse supports clinical research operations by delivering direct ... Ensure pharmacokinetic rooms and clinical spaces are clean, stocked, and patientready. * Maintain ...

The Associate Clinic Research Nurse supports clinical research operations by delivering direct ... Ensure pharmacokinetic rooms and clinical spaces are clean, stocked, and patientready. * Maintain ...

The Associate Clinic Research Nurse supports clinical research operations by delivering direct ... Ensure pharmacokinetic rooms and clinical spaces are clean, stocked, and patientready. * Maintain ...

The Associate Clinic Research Nurse supports clinical research operations by delivering direct ... Ensure pharmacokinetic rooms and clinical spaces are clean, stocked, and patient‑ready.

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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 Aug 24, 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 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.

What are the key skills and qualifications needed to thrive as an entry level pharmacovigilance associate?

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 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 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.

How do I enter into an entry level pharmacovigilance associate role?

To enter an entry-level pharmacovigilance associate role, candidates typically need a bachelor's degree in life sciences, pharmacy, or a related field. Relevant skills include attention to detail, knowledge of adverse event reporting, and familiarity with regulatory guidelines like ICH E2E. Gaining experience through internships or certifications such as the Drug Safety and Pharmacovigilance Certification can improve job prospects.

Is an entry level pharmacovigilance associate a stressful job?

An entry level pharmacovigilance associate typically works in a regulated environment monitoring drug safety, which can involve tight deadlines and detailed data review. While the role can be demanding, it generally involves routine tasks and the use of specialized software, making stress levels manageable with proper training and organization.

What is the role of an entry level pharmacovigilance associate?

An entry level pharmacovigilance associate is responsible for monitoring, detecting, and reporting adverse drug reactions and safety issues related to pharmaceutical products. They review safety data, maintain documentation, and ensure compliance with regulatory requirements using tools like safety databases. This role often requires attention to detail, knowledge of medical terminology, and familiarity with pharmacovigilance processes.

What qualifications do I need for entry level pharmacovigilance associate?

An entry-level pharmacovigilance associate typically needs a bachelor's degree in pharmacy, medicine, life sciences, or a related field. Strong attention to detail, good communication skills, and familiarity with medical terminology and safety databases are also important; some roles may require basic knowledge of regulatory guidelines like ICH E2E or Good Pharmacovigilance Practices (GVP).
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Infographic showing various Entry Level Pharmacovigilance Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 29% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

Associate Scientist I LCMS (entry level-new graduate- chemistry)

Malvern, PA • On-site

Other

Posted 9 days ago


Job description

Job Description

Resolian is a Contract Research Organization (CRO) specializing in Drug Metabolism and Pharmacokinetic (DMPK) and bioanalytical services for both small and large molecules.

At Resolian, we work to bring together and develop exceptional employees and colleagues who share our passion for generating significant contributions to the world. We take pride in our work and our employees. Resolian strives to help you and your family by offering a comprehensive benefits package.Our total rewards are designed to recognize outstanding performance and meet the diversified needs of all our colleagues – at every stage of their professional and personal lives.

We continually strive to maintain the highest standards of professional ethics, scientific excellence, and regulatory compliance. We work to build trusted partnerships with each of our employees.

Please consider joining our experienced & knowledgeable staff. Resolian is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.

Responsibilities:

  • Prepare reagents, standards, and control samples
  • Analyze samples using various techniques specific to department
  • Assist with method development
  • Perform method validation or qualification
  • Operate analytical equipment
  • Lead troubleshooting activities
  • Maintain analytical equipment
  • Ensure lab area is clean and inspection ready at all times
  • Remove lab waste
  • Record tasks in accordance with Good Documentation Practices (GDP)
  • Understand and apply regulatory requirements; GLP, GCP, 21CFR Part 11
  • Follow applicable SOPs and procedural documents
  • Review and evaluate data results
  • Train lower level Scientists
  • Other tasks as assigned

Education, Experience & Skills Required:

  • BA/BS or higher with 0-2 years lab experience; all experiences will be evaluated
  • Able to work in a regulated environment
  • Able to work effectively and contribute within a team
  • Able to work with computer systems
  • Able to document clearly; knowledge of and experience in a regulatory environment


About Us

Are you interested in working in science for a leading global Contract Research Organization that is expanding rapidly and delivering best in class service to its clients? If you are ambitious and hard working then keep reading, as we are looking for talented individuals like you.

We are globally recognised for our leadership in science and, as a result, you will have the opportunity to work with some of our industries smartest and most inquisitive people, in a flexible and supportive environment. It is the ideal place to expand your knowledge, take on new responsibilities and make ambitious strides in your career.

If you want to join us to help us deliver our mission of using our scientific capabilities to improve the quality of life of people, then we would love to hear from you.