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Drug Safety Associate Jobs in Raleigh, NC (NOW HIRING)

Belcan

Drug Safety Coordinator

Clayton, NC · On-site

$19.23 - $26/hr

Associate degree * 2-3 years of recent experience in a clinical setting or equivalent in experience or training. * Clinical drug development experience preferred. If you are interested in this role ...

Block by Block

Safety Associate

Raleigh, NC · On-site

$22/hr

Safety Ambassador Pay Range: $22.00 to $22.00 per hour (Weekly Pay & Pay Advance Before Payday!) Shift/Schedule: * Weekend availability * 2:00pm to 10:30pm NC PPSB Guard Card REQUIRED First Aid + CPR ...

AA2IT

Medical Device Vigilance professionals

Raleigh, NC · On-site

$40 - $42/hr

Bachelor's degree in a science or health care-related field or RN/PharmD * 5+ years of experience in drug safety or medical device vigilance (preferred) in an industry setting or equivalent Preferred ...

micro1 AI

Pharmacovigilance Expert

Cary, NC · 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

Durham, NC · 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

Raleigh, NC · 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 ...

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All JobsDrug Safety Associate JobsDrug Safety Associate Jobs in Raleigh, NC

Drug Safety Associate information

See Raleigh, NC salary details

$11

$47

$83

How much do drug safety associate jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for drug safety associate in Raleigh, NC is $47.77, according to ZipRecruiter salary data. Most workers in this role earn between $37.40 and $53.99 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.

More about Drug Safety Associate jobs

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The most popular types of Drug Safety jobs in Raleigh, NC are:

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For Drug Safety Associate jobs in Raleigh, NC, the most frequently searched job titles are:

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The top searched job categories for Drug Safety Associate jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Drug Safety Associate jobs?

Cities near Raleigh, NC with the most Drug Safety Associate job openings:

Drug Safety Associate jobs near you
Infographic showing various Drug Safety Associate job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 73% In-person, and 27% Remote job distribution, with an average salary of $99,357 per year, or $47.8 per hour.

Drug Safety Coordinator

Belcan

Clayton, NC • On-site

$19.23 - $26/hr

Full-time

Posted 20 days ago

Job description

Job Title: Drug Safety Coordinator
Location: Clayton, NC
Pay rate: $19.23 - 26/hr.
Zip Code: 27520
Area Code: 919, 984
Start Date: Right Away
Shift: 8:30 AM-5:00 PM
Keywords: #ClaytonJobs; #DrugSafetyCoordinatorJobs;
Job Description
The incumbent is required to be an independent contributor that efficiently and effectively accomplishes drug safety tasks and deliverables with little oversight. Prefer if they have ARGUS/safety database experience. As Global Drug Safety team member, DSC obtains and processes all appropriate information regarding adverse event data to maintain a thorough and strict adherence to Good Clinical Practices (GCP), regulatory guidelines, and company SOPs. Assists Drug Safety Scientist (DSS) and management in building team environment among assigned staff and between other departments.
Primary responsibilities:
* Identify, track, and file potential adverse event (AE) information.
a. Responsible for monitoring all incoming information and identification of potential AE information and assembling data for team meetings.
b. Enter the report into the tracking log, check whether it is an initial, a follow-up, or a duplicate report and creates a case folder.
c. Identify and delete all confidential patient information from the source documents received.
d. Record protocol number and site/patient number, if applicable, on all source documents.
e. Provide the report to the conducting case owner
* Identify, track, and file potential adverse event (AE) information.
Additional responsibilities:
* The Drug Safety Coordinator is the first person in Global Pharmacovigilance to review the source documents for AE reports.
* As such, the DSC makes the first determination of report completeness and the need to perform follow-up with the reporter.
* Maintains a basic understanding of the protocol and scope of work for clinical studies.
* Maintains a thorough understanding and strict adherence to GCP guidelines and regulatory reporting regulations.
* Responsible for management of receipt, review and filing of literature sources that may contain AE information.
Knowledge, Skills, and Abilities:
* Excellent technical skills required, including the ability to comprehend and integrate scientific data from a variety of sources.
* Comprehensive knowledge of medical terminology required.
* Excellent interpersonal, organizational, and prioritization skills.
* Flexibility and the ability to multitask is mandatory.
* Strong computer literacy required.
Requirements:
* Associate degree
* 2-3 years of recent experience in a clinical setting or equivalent in experience or training.
* Clinical drug development experience preferred.
If you are interested in this role, please apply via the apply now link provided. Our overriding goal is to provide quality staffing solutions that help people, organizations, and communities succeed. Belcan is a leading provider of qualified personnel to many of the world's most respected enterprises. We offer excellent opportunities for contract, temporary, temp-to-hire, and direct assignments. We are the employer of choice for thousands worldwide. For more information, please visit our website at Belcan.com
Belcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.
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About Belcan

Sourced by ZipRecruiter

Belcan is a leading provider of qualified personnel to many of the world's most respected enterprises. We offer excellent opportunities for contract/temporary, temp-to-hire, and direct assignments in the engineering, IT, and professional fields. We are the employer of choice for thousands worldwide. Our overriding goal is to provide quality staffing solutions that help people, organizations, and communities succeed.

Industry

It services

Company size

5,001 - 10,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1958

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