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Drug Safety Coordinator Jobs (NOW HIRING)

Belcan

Drug Safety Coordinator

Clayton, NC

$19.23 - $26/hr

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 ...

Viking Therapeutics

Drug Safety Associate

San Diego, CA · On-site

$77K - $90K/yr

Minimum of 1-3 years of relevant experience in clinical research, drug safety/pharmacovigilance, clinical trial coordination, clinical data management, or a related function within a biotechnology ...

Integrated Resources INC

Drug Safety

Horsham, PA · On-site

Triage of incoming cases to determine seriousness for prioritization of daily workflow (to be discussed re triage specialist) Confirmation of Safety Coordinator case registry data Database searches ...

KW Electric

Safety Coordinator

Emmetsburg, IA · On-site

Coordinate drug testing for new hires and per workplace policy * Inspect and document safety ... Experience as a Safety Coordinator or in a safety support role preferred * First aid/CPR ...

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How much do drug safety coordinator jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for drug safety coordinator in the United States is $24.28, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $27.40 per hour, depending on experience, location, and employer.

What is a drug safety coordinator?

Drug Safety Coordinators are professionals who manage and oversee the collection, processing, and reporting of information related to the safety of pharmaceutical products. They play a crucial role in pharmacovigilance by ensuring that adverse drug reactions are properly documented and communicated to regulatory authorities. Their work helps to identify potential risks associated with medications, contributing to patient safety and compliance with legal requirements. Drug Safety Coordinators often collaborate with healthcare professionals, regulatory agencies, and pharmaceutical companies to maintain the highest safety standards.

What does a drug safety coordinator do?

A drug safety coordinator handles cases related to pre-and postmarketing of FDA-regulated products. In this career, you enter and interpret individual reports including lab results, known issues, and consumer complaints about adverse effects. You must have a keen attention to detail to follow compliance regulations to the letter. You work under the direction of a manager who assigns you cases and gives you responsibilities. Other duties of this position are to work with other agencies and individuals to compile the data. You must document all procedures and produce detailed narratives of findings. Familiarity with related software is crucial, along with medical safety coding.

What are the key skills and qualifications needed to thrive as a drug safety coordinator, and why are they important?

To thrive as a Drug Safety Coordinator, you need a background in life sciences or pharmacy, strong knowledge of pharmacovigilance processes, and familiarity with regulatory requirements. Proficiency with safety databases (such as Argus or ARISg), MedDRA coding, and relevant pharmacovigilance software is typically required. Attention to detail, effective communication, and strong organizational skills help you manage safety data and collaborate with cross-functional teams. These skills and qualities are crucial for ensuring accurate reporting, regulatory compliance, and the protection of patient safety throughout the drug lifecycle.

How does a drug safety coordinator typically collaborate with other departments within a pharmaceutical company?

A Drug Safety Coordinator works closely with various teams, such as clinical research, regulatory affairs, and medical affairs, to ensure thorough monitoring and reporting of adverse drug events. Communication is key, as the coordinator must gather information from clinical sites, relay findings to regulatory teams, and sometimes participate in cross-functional safety meetings. This collaboration helps maintain compliance with safety regulations and supports the ongoing evaluation of product risk-benefit profiles. Strong teamwork and organizational skills are essential for success in this role.

What is the difference between Drug Safety Coordinator vs Pharmacovigilance Specialist?

AspectDrug Safety CoordinatorPharmacovigilance Specialist
CredentialsCertification in drug safety or pharmacovigilance often preferredSimilar certifications, often requiring pharmacovigilance training
Work EnvironmentPharmaceutical companies, CROs, healthcare settingsPharmaceutical companies, regulatory agencies, CROs
Industry UsageCommonly used in clinical and post-marketing safetyFocuses on drug safety monitoring and adverse event analysis
Search/Comparison IntentOften compared for roles in drug safety teamsRelated but more specialized in safety data analysis

The main difference is that a Drug Safety Coordinator manages and tracks adverse events and safety reports, ensuring compliance with regulations. A Pharmacovigilance Specialist typically performs more in-depth safety data analysis and signal detection. Both roles require similar certifications and work in similar environments, but the Pharmacovigilance Specialist often has a more analytical focus.

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Drug Safety Coordinator jobs near you
Infographic showing various Drug Safety Coordinator job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 16% Part Time, 1% Contract, and 1% Nights. Highlights an 98% Physical, and 2% Remote job distribution, with an average salary of $50,507 per year, or $24.3 per hour.

Drug Safety Coordinator

Clayton, NC

Belcan
IT Services • 5 - 10K employees
Learn more about Belcanexternal

$19.23 - $26/hr

Full-time

Posted 24 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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