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Drug Safety Associate Jobs (NOW HIRING)

Biogen

Sr Associate II, Drug Safety

Cambridge, MA · On-site

$106K - $138K/yr

The Sr Associate II, Drug Safety is accountable for the end-to-end operational management of Adverse Events of Special Interest (AESIs) across the product lifecycle, including both Clinical Trial and ...

Biogen

Sr Associate II, Drug Safety

Cambridge, MA

$106K - $138K/yr

The Sr Associate II, Drug Safety is accountable for the end-to-end operational management of Adverse Events of Special Interest (AESIs) across the product lifecycle, including both Clinical Trial and ...

Global Pharmatek

NJ

Global Pharma Tek offers services like Drug Discovery, Clinical Trials, Drug Delivery, Regulatory ... Enter applicable information into the global safety database for initial or follow up cases ...

Gifthealth

Drug Safety Specialist I, II, III

Columbus, OH · On-site

$23 - $31/hr

Position Summary The Drug Safety Specialist I, II, & III - Product Replacement is responsible for the intake, investigation, documentation, and execution of medication replacement events resulting ...

Global Pharmatek

Drug Safety Assistant

Piscataway, NJ · On-site

Global Pharma Tek offers services like Drug Discovery, Clinical Trials, Drug Delivery, Regulatory ... Enter applicable information into the global safety database for initial or follow up cases ...

Crispr Therapeutics

Senior Manager, Drug Safety

Boston, MA · On-site

$140K - $155K/yr

Train drug safety teams on established procedures and oversee compliance * Serve as the subject matter expert for ICSR intake processes and regulatory expectations, including presentations for ...

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Drug Safety Associate information

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$12

$49

$85

How much do drug safety associate jobs pay per hour?

As of Jun 28, 2026, the average hourly pay for drug safety 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.

How does a Drug Safety Associate typically collaborate with other teams during the drug development process?

Drug Safety Associates regularly work in close coordination with clinical research, regulatory affairs, and medical affairs teams. They are responsible for collecting, evaluating, and reporting adverse event data, which often requires clear communication with clinical trial staff and investigators. Additionally, they may participate in cross-functional safety review meetings to discuss safety findings and ensure compliance with regulatory requirements. This collaborative environment helps ensure comprehensive safety monitoring throughout the drug's lifecycle.

What Does a Drug Safety Associate Do?

A drug safety associate works in the medical industry to monitor the safety of pharmaceutical drugs and to evaluate and prevent adverse reactions in patients. A career in drug safety, also called pharmacovigilance, can include work with clinical research organizations that conduct trials, biotechnology firms, pharmaceutical companies, or government agencies like the National Institutes of Health (NIH). Drug safety associates need excellent research skills, a strong background in medical or biological science, and in-depth knowledge of the Food and Drug Administration (FDA) regulations. Your responsibilities include analyzing clinical trial data, writing reports, and determining whether specific pharmaceutical drugs are safe.

What are Drug Safety Associates?

Drug Safety Associates are professionals responsible for monitoring and evaluating the safety of pharmaceutical products. They collect, analyze, and report data on adverse drug reactions to ensure compliance with regulatory requirements and to protect patient safety. Their work involves reviewing case reports, maintaining safety databases, and communicating safety information to regulatory agencies and healthcare professionals. Drug Safety Associates play a vital role in the pharmacovigilance process throughout the lifecycle of a drug.

What is the difference between Drug Safety Associate vs Pharmacovigilance Specialist?

AspectDrug Safety AssociatePharmacovigilance Specialist
CredentialsTypically requires a degree in life sciences or healthcare, with certifications like PV or drug safety trainingSimilar credentials, often with additional certifications or experience in pharmacovigilance
Work EnvironmentPharmaceutical companies, CROs, or healthcare settings focusing on safety data managementSame as Drug Safety Associate, often with more specialized pharmacovigilance tasks
Employer & IndustryPharmaceutical, biotech, and healthcare industriesSame industries, with a focus on drug safety monitoring and compliance

Both roles involve monitoring drug safety data, reporting adverse events, and ensuring regulatory compliance. The main difference lies in the scope and specialization, with Pharmacovigilance Specialists often handling more complex safety data analysis and regulatory submissions. However, the roles overlap significantly, and job titles are sometimes used interchangeably depending on the organization.

What are the key skills and qualifications needed to thrive as a Drug Safety Associate, and why are they important?

To thrive as a Drug Safety Associate, you need a solid background in life sciences or pharmacy, knowledge of pharmacovigilance principles, and attention to detail. Familiarity with drug safety databases (such as Argus or ARISg), MedDRA coding, and regulatory reporting systems is typically required. Strong organizational skills, effective communication, and the ability to work under deadlines help you excel in collaborating with cross-functional teams. These skills ensure accurate adverse event reporting, regulatory compliance, and protection of patient safety throughout the drug development lifecycle.
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Drug Safety Associate jobs near you
Infographic showing various Drug Safety Associate job openings in the United States as of June 2026, with employment types broken down into 55% Full Time, 39% Part Time, 4% Contract, and 2% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.
Entry level - Drug Safety

Entry level - Drug Safety

Integrated Resources INC

Foster City, CA

Contractor

Posted 7 days ago

Job description

Job Description
  • Sets work priorities and direction with input from Manager.
  • Responsible for the accurate and timely book-in and acknowledgement of adverse event information in compliance with applicable SOPs and guidelines.
  • Understand SDEA and global regulatory reporting timelines in order to prioritize cases if needed.
  • Perform simple queries of the safety database, e.g. duplicate searches.
  • Maintain and manage dept. Safety mailbox, distributing to relevant parties as applicable.
  • May perform initial data entry of ICSRs (review, extract, accurately enter AE data from ICSR reports).
  • May interpret case-related information including medical conditions, lab results and procedures, as well as compile complete narrative summaries.
  • Meet specific data and quality targets for case handling
  • Assist with tracking and reconciliation of incoming adverse event reports.
  • Coordinate submission of product complaints to the Quality assurance department.
  • Participate in department projects, as required and will be cross-trained to handle other functions as deemed necessary
  • Recognizes situations that require assistance from more senior staff members and seeks assistance from appropriate internal and external resources.
  • Assists Safety Specialists in sending and tracking follow-up letters.
  • Remain current with case handling SOPs, guidance documents and database technology
  • May assist manager in the preparation of training material and assist in training new employees their functional area.
  • May assist manager with writing/reviewing guidelines for their functional area of expertise.
  • May assist with other projects as necessary (i.e., study unbinding, reconciliation with vendors, etc)
  • Ensures departmental workflow processes and timelines are followed
  • Knowledge, Experience and Skills:
  • Excellent interpersonal communication skills, both written and oral
  • Excellent computer skills in Microsoft environment (Microsoft Excel, Power point and Word).
  • Safety database and data entry experience preferred
  • Basic understanding of medical and drug terminology preferred
  • JD - Drug Safety & Public Health, Operations
  • Knowledge and experience with safety reporting and regulatory compliance and experience with international safety reporting/regulations is preferred
  • Demonstrates initiative, teamwork and accountability
  • Demonstrated success working both independently and in collaboration with others
  • A quality driven individual with strong attention to detail and accuracy is required
  • Strong organizational skills, and ability to adapt to change
  • A demonstrated ability to manage own workload, prioritize, plan and organize assignments and work under stick timelines is required.
  • Ability to follow guidelines and procedural documents
  • AA or BS degree (or equivalent experience) and little to no experience.
  • Industry experience in the health, clinical, bio-pharmaceutical, or relevant industries such as, pharmacy technician, nursing assistant is valuable but not required.
Additional Information

All your information will be kept confidential according to EEO guidelines.

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About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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