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Drug Safety Associate Jobs (NOW HIRING)

Integrated Resources INC

Drug Safety

Horsham, PA

Triage of incoming cases to determine seriousness for prioritization of daily workflow (to be discussed re triage specialist) Confirmation of Safety Coordinator case registry data Database searches ...

Grifols

Drug Safety Scientist

Clayton, CA · On-site

They will be responsible for providing oversight to Drug Safety Coordinators and the case intake ... Associate's degree with 6 years of experience, or a Master's degree with 2 years of experience.

GRIFOLS, S.A.

Drug Safety Scientist

Clayton, NC · On-site

They will be responsible for providing oversight to Drug Safety Coordinators and the case intake ... Associate's degree with 6 years of experience, or a Master's degree with 2 years of experience.

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 ...

Global Pharmatek

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 ...

Actalent

Drug Safety Manager

South San Francisco, CA · On-site

Job Title: Senior Drug Safety Case Manager The Senior Drug Safety Case Manager supports both clinical trial and post-marketing pharmacovigilance activities within a growing pharmaceutical ...

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 ...

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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 Jul 22, 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.

What is the role of a drug safety associate?

A drug safety associate is responsible for monitoring, assessing, and reporting adverse drug reactions and safety issues related to pharmaceutical products. They review clinical data, ensure compliance with regulatory requirements, and contribute to pharmacovigilance activities to protect patient safety. Strong attention to detail and knowledge of regulatory guidelines are essential in this role.

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.

How much do drug safety associates make in the US?

Drug safety associates in the US typically earn a median annual salary of around $70,000 to $90,000, depending on experience, location, and certifications. Entry-level positions may start lower, while experienced professionals with specialized skills can earn higher salaries, often with opportunities for bonuses and benefits.

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.

How to become a drug safety associate?

To become a drug safety associate, candidates typically need a bachelor's degree in pharmacy, life sciences, or a related field. Relevant skills include knowledge of pharmacovigilance processes, attention to detail, and familiarity with safety databases; certifications like the Drug Safety Certification (DSC) can enhance prospects.

What is the highest paid safety job?

In the field of drug safety, senior roles such as Drug Safety Director or Pharmacovigilance Director tend to be the highest paid, often earning six-figure salaries. These positions require extensive experience, leadership skills, and knowledge of regulatory requirements, and they oversee safety programs and compliance for pharmaceutical companies.
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Drug Safety Associate jobs near you
Infographic showing various Drug Safety Associate job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% 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.
Drug Safety

Drug Safety

Integrated Resources INC

Horsham, PA

Contractor

Posted 11 days ago

Job description

Company Description

A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.



Job Description

Case Processing: 75% of time Definition: The completion of full case information on the database, culminating in Quality Review to ensure accuracy and completeness. Activities Include: Triage of incoming cases to determine seriousness for prioritization of daily workflow (to be discussed re triage specialist) Confirmation of Safety Coordinator case registry data Database searches as necessary Completion of literature searches as necessary Completion of remaining case data entry, including narrative or auto-narrative Completion of risk and quality (label, approval, manual coding & quality review steps) Clarification of unclear or illegible information from the LSO or Call Centre Discuss source documents, coding conventions and ad-hoc queries with Medical Assessment Physician Completion of protocol request forms as necessary Preparation of deviation memo as necessary Request deletions as necessary Single case unblinding Processes and Procedures: 5% of time Definition: Continuing awareness of company procedures and guidelines to maintain regulatory compliance. Activities Include: Standard Operating Procedures and Working Practices Department guidance documents MedDRA coding dictionary and MedDRA points to consider Understand relevant safety implications regarding contracts with operating companies and/or marketing partners Review and make suggestions for system and procedure enhancements 5% of time = Project Work, Audits, Inspections and other Ad-hoc


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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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