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Drug Safety Associate Jobs in Silver Spring, MD (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.

micro1 AI

Pharmacovigilance Expert

Alexandria, VA · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next ...

micro1 AI

Pharmacovigilance Expert

Washington, DC · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next ...

micro1 AI

Pharmacovigilance Expert

Baltimore, MD · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next ...

Emmes Group

Sr. Safety Monitor I

Rockville, MD · On-site

Overview Sr. Safety Monitor I Be Part of One Team, One Purpose. At Emmes Group , we're shaping the ... Working knowledge of MedDRA and WHO Drug coding preferred. * Demonstrated use of medical ...

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All JobsDrug Safety Associate JobsDrug Safety Associate Jobs in Silver Spring, MD

Drug Safety Associate information

See Silver Spring, MD salary details

$12

$50

$88

How much do drug safety associate jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for drug safety associate in Silver Spring, MD is $50.80, according to ZipRecruiter salary data. Most workers in this role earn between $39.76 and $57.40 per hour, depending on experience, location, and employer.

What is a drug safety associate?

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 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 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 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 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.

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Drug Safety Associate jobs near you
Infographic showing various Drug Safety Associate job openings in Silver Spring, MD as of August 2026, with employment types broken down into 100% Full Time. Highlights an 66% In-person, and 34% Remote job distribution, with an average salary of $105,749 per year, or $50.8 per hour.

S & P Associate

Technical Resources International, Inc

Bethesda, MD • On-site

Full-time

Re-posted 27 days ago

Key responsibilities

  • Collect, organize, and interpret safety-related data to support project-specific safety operations.

  • Manage safety-related communications, including safety reports, adverse event notifications, and updates, to relevant stakeholders.

  • Maintain and organize safety documentation and oversee safety box management to ensure compliance and accessibility.

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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