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Drug Safety Associate Jobs (NOW HIRING)

Nurix

Medical Director, Drug Safety

Brisbane, CA

Medical Director, Drug Safety Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines ...

Nurix

Medical Director, Drug Safety

Brisbane, CA · On-site

Medical Director, Drug Safety Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines ...

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All JobsDrug Safety Associate Jobs

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.
Senior Pharmacovigilance System Architect (Argus Administrator) - US

Senior Pharmacovigilance System Architect (Argus Administrator) - US

MMS

Chicago, IL • On-site

Full-time

Posted 6 days ago

Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.

Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.

Senior Pharmacovigilance System Architect

We are recruiting for an experienced Pharmacovigilance System Architect (Argus Administrator SME) to join our US team.

Roles & Responsibilities

  • Serves as Database Administrator for Argus Safety, including database configuration, issue resolution, maintenance, governance and daily support.
  • Performs installations, upgrades, configuration of reporting rules, and E2B reporting via gateway technologies (including set-up and configuration of Axway Gateway Interchange).
  • Provides support for all systems associated with PV and drug safety.
  • Performs updates to Argus configuration and processes as per changing EudraVigilance regulations.
  • Provides support and execution of activities related to EudraVigilance testing for various clients.
  • Performs case migration/database transfers, file importing and supports other case processing activities.
  • Provides leadership in executing Argus upgrades and related activities.
  • Provides administrator support for other safety databases (such as ARISg).
  • Performs periodic coding dictionary (MedDRA & WHO drug) updates for Argus.
  • Provides technical assistance and support to Drug Safety Associate team with electronic submissions of serious adverse advents to European agencies.
  • Writes procedural documents including Standard Operating Procedures (SOP), Work Practice Documents, and Data Entry Manuals for Argus Safety.
  • Generates case processing metrics, reviews and makes suggestions and supports process improvement implementation.
  • Maintains technical expertise of regulatory requirements and ensures alignment with company working practices.
  • Assists with business development and capabilities efforts as needed.
  • Interacts directly and independently with client to coordinate all facets of projects; competent communicator, supports client capabilities as PV/drug safety systems SME.
  • Strong understanding and experience working with Argus configuration and study set up.
  • Strong understanding of global case processing and SAE reporting.
  • Strong understanding of global clinical trial development and data.

Requirements

  • College graduate Information Technology discipline or related field, or relevant experience.
  • Minimum of 5 years’ experience in Information Technology or similar field required.
  • Expert knowledge of scientific principles and concepts.
  • Reputation as emerging leader in field with sustained performance and accomplishment.
  • Proficiency with MS Office applications.
  • Hands-on experience with clinical trial and pharmaceutical development preferred.
  • Good communication skills and willingness to work with others to clearly understand needs and solve problems.
  • Excellent problem-solving skills.
  • Good organizational and communication skills.
  • Familiarity with current ISO 9001 and ISO 27001 standards preferred.
  • Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
  • Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.

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About M. M. S.

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

Los Angeles, CA, US

Year founded

1980

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