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Drug Safety Associate Jobs in Reston, VA (NOW HIRING)

TRI Challenge Convention

S & P Associate

Bethesda, MD · Hybrid

The Safety Associate focuses on managing and analyzing safety-related data under supervision ... General knowledge of the drug and vaccine development process or clinical trials is a plus. B.A./B.

Diversified Safety Services

Safety Manager

Manassas, VA · On-site

$45 - $55/hr

Safety Manager Location: Northern, VA Start Date: ASAP Pay Range: $45.00/hr- $55.00/hr Per diem available if a traveler Diversified Safety Services is seeking an experienced Site Safety Manager to ...

Diversified Safety Services

Safety Manager

Bristow, VA · On-site

Company Description Diversified Safety Services is a full-service occupational safety and health consulting firm providing safety audits, full time safety officers, safety trainings, accident ...

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All JobsDrug Safety Associate JobsDrug Safety Associate Jobs in Reston, VA

Drug Safety Associate information

See Reston, VA salary details

$12

$51

$89

How much do drug safety associate jobs pay per hour?

As of Jul 22, 2026, the average hourly pay for drug safety associate in Reston, VA is $51.13, according to ZipRecruiter salary data. Most workers in this role earn between $40.00 and $57.79 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.
More about Drug Safety Associate jobs
What are popular job titles related to Drug Safety Associate jobs in Reston, VA? For Drug Safety Associate jobs in Reston, VA, the most frequently searched job titles are:
What job categories do people searching Drug Safety Associate jobs in Reston, VA look for? The top searched job categories for Drug Safety Associate jobs in Reston, VA are:
What cities near Reston, VA are hiring for Drug Safety Associate jobs? Cities near Reston, VA with the most Drug Safety Associate job openings:
Drug Safety Associate jobs near you
Infographic showing various Drug Safety Associate job openings in Reston, VA as of July 2026, with employment types broken down into 1% As Needed, 71% Full Time, 25% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $106,342 per year, or $51.1 per hour.
S & P Associate

S & P Associate

Technical Resources International, Inc

Bethesda, MD • On-site

Full-time

Posted 13 days ago

Job description

Job Title
S & P Associate
Location
Bethesda, MD 20817 US (Primary)
Category
Drug Safety
Job Type
Full-Time
Salary Range
54,000.00-60,000.00/YEAR
Education
Bachelor's Degree
Travel
None
Job Description
  • The Safety Associate is essential for collecting, organizing, and interpreting data accurately to support project-specific safety operations. The Safety Associate focuses on managing and analyzing safety-related data under supervision
  • Responsible for ensuring data accuracy and completeness by validating entries and resolving discrepancies during SAE process.
  • Work closely with Safety Specialists, Managers, Physicians and Medical Monitors, and cross-functional teams to provide accurate data and reports for analysis.
  • Assist in meetings and presentations by preparing data summaries or supporting materials.
  • Responsible for Safety-Related Distributions: Manage and distribute safety-related communications, such as safety reports, adverse event notifications, and updates, to relevant stakeholders, including study sites, investigators, and regulatory authorities.
  • Responsible for Site Communications: Serve as a liaison for safety-related communications between study sites and the safety team. Ensure timely and accurate communication of safety issues, clarifications, or updates to clinical sites.
  • Responsible for Document Control: Maintain and organize safety documentation, ensuring that all safety-related records (e.g., SAE reports, safety letters, regulatory submissions) are stored, tracked, and updated in compliance with project-specific and regulatory requirements.
  • Responsible for Safety Box Management: Oversee the maintenance and tracking of safety boxes, ensuring all required documents and safety reports are available, properly archived, and readily accessible.
  • Tracking Compliance: Monitor the distribution and receipt of safety-related documents to ensure compliance with project timelines and regulatory guidelines. Track the status of safety reports, document submissions, and follow-ups.
  • This role is essential for ensuring that all safety-related documents and communications are managed systematically, ensuring compliance with regulatory and project-specific standards.
  • Experienced Safety Associates are responsible for performing MedDRA coding and processing Serious Adverse Events (SAEs) to contribute to the development of comprehensive safety reports.

Job Requirements
  • Must have excellent attention to detail, verbal and written communication skills.
  • Superior organizational skills and customer service abilities are required.
  • Proficiency in MS Office (Word, Excel, and Outlook); experience with SharePoint is a plus.
  • General knowledge of the drug and vaccine development process or clinical trials is a plus.
  • B.A./B.S. Degree
  • This is a hybrid position with 2 days in TRI's Bethesda, Maryland office, and 3 days working remotely.

We are equal opportunity/affirmative action employers, committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status, or any other protected characteristic under state or local law.

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