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Entry Level Drug Safety Associate Jobs in Reston, VA

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.

Alliance Workforce

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Warehouse Associate

Sterling, VA · On-site

$18/hr

... Entry-Level Warehouse Associate . This is an excellent opportunity for someone looking to start or grow a career in warehouse and logistics with a stable company that values teamwork, safety, and ...

ServeFed

Accountant - Entry Level

Germantown, MD

... safety, and workforce management. Join our talent community today and build a rewarding career ... Must have graduated with an Associate Degree in Accounting within the last 3 years; Bachelor ...

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Entry Level Drug Safety Associate information

See Reston, VA salary details

$12

$51

$89

How much do entry level drug safety associate jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for entry level 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 difference between Entry Level Drug Safety Associate vs Drug Safety Specialist?

AspectEntry Level Drug Safety AssociateDrug Safety Specialist
CredentialsBachelor's degree in life sciences or related field; some certifications preferredSimilar educational background; often requires additional certifications or experience
Work EnvironmentPharmaceutical companies, CROs, or healthcare settings; entry-level rolesMore experienced roles within similar environments, handling complex safety data
ResponsibilitiesData entry, case processing, basic safety reportingIn-depth safety analysis, signal detection, and regulatory reporting

The Entry Level Drug Safety Associate typically handles foundational safety data tasks, while the Drug Safety Specialist performs more advanced safety analysis and regulatory responsibilities. Both roles are essential in pharmacovigilance, with the associate serving as an entry point and the specialist focusing on complex safety evaluations.

What are the key skills and qualifications needed to thrive as an entry level drug safety associate, and why are they important?

To thrive as an Entry Level Drug Safety Associate, you generally need a bachelor's degree in life sciences, pharmacy, or a related field, along with foundational knowledge of pharmacovigilance principles. Familiarity with safety databases such as Argus or ARISg, and understanding of regulatory guidelines like ICH and MedDRA coding, are often required. Attention to detail, strong organizational skills, and clear written communication help ensure accurate case processing and effective teamwork. These skills are crucial for maintaining regulatory compliance, ensuring patient safety, and supporting the integrity of drug safety data.

What does an entry level drug safety associate do?

An Entry Level Drug Safety Associate is responsible for supporting the collection, evaluation, and reporting of adverse drug reactions and other safety information related to pharmaceutical products. They help ensure compliance with regulatory requirements by processing case reports, entering data into safety databases, and assisting with safety documentation. This role often involves collaborating with clinical teams and regulatory authorities to help maintain the safety profile of medications on the market.

What are some common challenges faced by entry level drug safety associates, and how can they be managed?

Entry level Drug Safety Associates often encounter challenges such as managing large volumes of case reports, adhering to strict regulatory timelines, and ensuring meticulous attention to detail in data entry and documentation. Working within cross-functional teams, they may need to quickly learn complex medical terminology and reporting systems. To manage these challenges, it's important to leverage available training, actively seek feedback from experienced colleagues, and develop strong organizational skills to prioritize tasks effectively. Building familiarity with pharmacovigilance software and regulatory requirements will also enhance efficiency and confidence in the role.
What are popular job titles related to Entry Level Drug Safety Associate jobs in Reston, VA? For Entry Level Drug Safety Associate jobs in Reston, VA, the most frequently searched job titles are:
What job categories do people searching Entry Level Drug Safety Associate jobs in Reston, VA look for? The top searched job categories for Entry Level Drug Safety Associate jobs in Reston, VA are:
What cities near Reston, VA are hiring for Entry Level Drug Safety Associate jobs? Cities near Reston, VA with the most Entry Level Drug Safety Associate job openings:
Entry Level Drug Safety Associate jobs near you
Infographic showing various Entry Level Drug Safety Associate job openings in Reston, VA as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 19% Part Time, 2% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $106,342 per year, or $51.1 per hour.

S & P Associate

Technical Resources International, Inc

Bethesda, MD • On-site

Full-time

Re-posted 4 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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