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Entry Level Drug Safety Associate Jobs (NOW HIRING)

Must pass a pre-employment drug screen and successfully participate in the program's mandatory ... Prior Safety Service Patrol Operator experience. * Knowledge/experience of incident management ...

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.

As a Patient Safety Associate, you will be working primarily in the Emergency Department but can be ... EEO/Disabled/Veterans Our organization supports a drug-free work environment. Privacy Policy:

Administer drug testing. * Administer basic First Aid. * Lead safety meetings. Requirements: * Possess specified certifications, including, but not limited to OSHA 30. * Demonstrate knowledge of ...

Administer drug testing. * Administer basic First Aid. * Lead safety meetings. Requirements: * Possess specified certifications, including, but not limited to OSHA 30. * Demonstrate knowledge of ...

As a Patient Safety Associate, you will be working primarily in the Emergency Department but can be ... EEO/Disabled/Veterans Our organization supports a drug-free work environment. Privacy Policy:

As a Patient Safety Associate, you will be working primarily in the Emergency Department but can be ... EEO/Disabled/Veterans Our organization supports a drug-free work environment. Privacy Policy:

Showing results 41-60

Entry Level Drug Safety Associate information

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$12

$49

$85

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

As of Aug 12, 2026, the average hourly pay for entry level 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 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.
More about Entry Level Drug Safety Associate jobs
What cities are hiring for Entry Level Drug Safety Associate jobs? Cities with the most Entry Level Drug Safety Associate job openings:
What states have the most Entry Level Drug Safety Associate jobs? States with the most job openings for Entry Level Drug Safety Associate jobs include:
Infographic showing various Entry Level Drug Safety Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, 2% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

Adverse Events and Product Complaints Lead

Gifthealth

Columbus, OH • On-site

$84K - $100K/yr

Full-time

Posted 25 days ago


Gifthealth rating

7.7

Company rating: 7.7 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

20th of 112 rated pharmacies


Job description

About Us
At Gifthealth, we're revolutionizing the way people experience healthcare by simplifying the process of managing prescriptions and health services. Our mission is to provide a seamless, personalized, and efficient healthcare experience for all our customers. We're a dynamic, innovative, and customer-centric company dedicated to making a positive impact on people's lives.
Position Summary
We are seeking an Adverse Events and Product Complaint (AEPC) Lead. Reporting to the Director of Pharmacy Quality & Compliance, the AEPC Lead oversees all adverse event and product complaint processes for the pharmacy, ensuring accurate documentation, timely submission, and full compliance with manufacturer and regulatory expectations. This role ensures all AE/PC cases are reviewed and submitted to our client(s) within the required timeframes. This position leads a small team of AEPC staff, coordinates with call center operations, and ensures AEPC records are properly entered and reconciled in the Quality Management System (QMS). The AEPC Lead identifies trends, escalates findings to the appropriate governing bodies, and upholds patient safety and regulatory integrity through continuous monitoring and reporting.
This position plays a key role in supporting the AEPC team, ensuring alignment with organizational goals, operational excellence, and compliance standards.
Key Responsibilities
  • Oversees the intake, documentation, and submission of all Adverse Events and Product Complaints to the client within 24-hour SLA requirements.
  • Completes monthly AEPC reconciliation with the client, ensuring all reports are logged, matched, and closed within compliance parameters
  • Maintains and update AEPC tracking and trending reports to identify recurring product or safety concerns; escalate trends to appropriate governing bodies.
  • Reviews and audit all AEPC tickets from the call center to ensure submissions are timely, accurate, and properly documented.
  • Schedules and leads AEPC team operations, ensuring coverage, adherence to SLAs, and accuracy in workload management.
  • Ensures all AEPC documentation is entered and maintained within the Quality Management System (QMS) for audit readiness and compliance traceability.
  • Serves as liaison between Gifthealth, the client, and compliance partners for all AEPC-related communication, training, and process improvement initiatives.
  • Supports compliance audits, ensuring all AEPC data and QMS records meet regulatory and manufacturer expectations.
Qualifications
  • Education: Bachelor's degree in pharmacy, nursing, life sciences, or related field (required)
  • Licensure/Certification: Certified Drug Safety Associate or equivalent pharmacovigilance certification (Preferred)
  • Experience:
  • Minimum 3 years of experience in adverse event reporting, pharmacovigilance, or product complaint management (Required)
  • AE/PC management within a regulated healthcare or pharmaceutical setting (Required)
  • Supervisory or scheduling responsibilities within compliance or quality teams (Preferred)
  • Experience with reconciliation or QMS systems used for safety documentation (Preferred)
  • Prior voice analytics and call center experience (Preferred)
  • Knowledge, Skills & Abilities:
  • Working knowledge of call center or intake workflows supporting AE/PC review
  • Knowledge of FDA AE/PC reporting requirements (21 CFR Parts 7, 211, 314.80, 600.80); Good Documentation Practices (GDP) and ALCOA principles; Call center workflows related to AEPC ticket triage; and QMS platforms and pharmacovigilance reporting systems (Required)
  • Knowledge of client's AE/PC systems and reconciliation procedures; ICH E2A and E2D guidelines for clinical safety data management; and ISO 13485 and post-market surveillance concepts (Preferred)
  • Strong organizational, leadership, and analytical skills (Required)
  • Excellent written and verbal communication (Required)
  • Proficiency in documentation management and QMS systems (Required)
  • Experience trending and analyzing AE/PC data for pattern recognition (Preferred)
  • Familiarity with Zendesk, Salesforce, or other ticketing/call center systems (Preferred)
  • Ability to lead and train drug safety team to meet strict submission SLAs (Required)
  • Ability to communicate effectively with manufacturers and regulatory agencies (Required)
  • Ability to manage competing deadlines with precision and urgency (Required)
  • Ability to develop AEPC dashboards and reconciliation reports for leadership visibility (Preferred)

Work Environment
  • Location: Hybrid/On-site
  • Schedule: Monday through Friday
  • May require availability during peak periods or flexibility for escalations.
  • Regular meetings with internal Compliance, Quality Assurance, Pharmacy Operations, and Call Center Teams. This role also interacts with client(s), the Food and Drug Administration (FDA) and other regulatory entities as needed.
Key Essential Functions
  • Must be able to stand for at least 4 hours at a time while working
  • Must be able to lift up to 25 pounds with or without assistance.
  • Must perform repetitive motions for an entire shift: bending, reaching, lifting, scanning.
  • Must be able to work onsite for all shifts.
Employment Classification
Status: Full-time
FLSA: Exempt
Equal Employment Opportunity (EEO) Statement
Gifthealth is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions are made without regard to race, color, religion, sex, sexual orientation, gender identity, transgender status, national origin, age, disability, veteran status, or any other legally protected status.
We celebrate diversity and are committed to creating an inclusive environment for all employees. If you do not meet every requirement but still feel you would be a great fit for this role, we encourage you to apply!
Disclaimer
This job description is intended to describe the general nature and level of work being performed. It is not intended to be an exhaustive list of all responsibilities, duties, or skills required of personnel. Gifthealth reserves the right to modify job duties or descriptions at any time.
Salary Description
$84,000-$100,000

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