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Contract Drug Safety Associate Jobs in Raleigh, NC

Belcan

Drug Safety Coordinator

Clayton, NC · On-site

$19.23 - $26/hr

Requirements: * Associate degree * 2-3 years of recent experience in a clinical setting or ... We offer excellent opportunities for contract, temporary, temp-to-hire, and direct assignments. We ...

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 ...

RXinsider LTD.

Senior Clinical Project Manager

Raleigh, NC · On-site

$140 - $200/hr

... Drug Safety, Regulatory, Data Management, Quality, and external vendors to ensure clinical trials ... Develop and manage study timelines, contract/budget negotiations, and risk mitigation plans to ...

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Contract Drug Safety Associate information

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$11

$47

$83

How much do contract drug safety associate jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for contract 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 does a contract drug safety associate do?

A Contract Drug Safety Associate is responsible for monitoring, collecting, and analyzing information about the safety of pharmaceutical products. They work on a contractual basis, often for pharmaceutical companies or clinical research organizations, to ensure that adverse events and potential side effects are properly documented and reported to regulatory authorities. Their duties may include data entry, case processing, regulatory reporting, and supporting safety audits. These professionals help ensure patient safety and compliance with regulatory requirements throughout the drug development and post-marketing process.

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

To thrive as a Contract Drug Safety Associate, you need a solid understanding of pharmacovigilance principles, adverse event reporting, and experience with regulatory guidelines, often supported by a degree in life sciences or pharmacy. Familiarity with drug safety databases (such as Argus or ARISg), MedDRA coding, and compliance with FDA and EMA regulations is typically required. Strong attention to detail, effective communication, and the ability to manage time-sensitive tasks are crucial soft skills in this role. These competencies ensure accurate safety data management, regulatory compliance, and the protection of patient well-being.

What are some common challenges faced by contract drug safety associates, and how can they be addressed?

Contract Drug Safety Associates often face challenges such as adapting quickly to new company protocols, managing high volumes of case processing within tight timelines, and staying updated with evolving regulatory requirements. Since contract roles may involve working with multiple teams or transitioning between projects, strong communication skills and adaptability are essential. Proactively seeking clarification, utilizing available training resources, and maintaining organized documentation can help overcome these challenges and ensure high-quality work in this fast-paced environment.

What is the difference between Contract Drug Safety Associate vs Contract Pharmacovigilance Associate?

AspectContract Drug Safety AssociateContract Pharmacovigilance Associate
CertificationsTypically requires life sciences or healthcare-related certificationsSimilar certifications, often including pharmacovigilance training
Work EnvironmentPharmaceutical companies, CROs, or biotech firmsSame as Drug Safety Associate, often in clinical or regulatory settings
Industry UsageUsed in drug safety monitoring and adverse event reportingUsed in drug safety, risk management, and regulatory compliance
Job FocusMonitoring adverse events, data entry, case processingMonitoring, reporting, and risk assessment of drug safety data

The Contract Drug Safety Associate and Contract Pharmacovigilance Associate roles are closely related, both focusing on drug safety and adverse event management within pharmaceutical and biotech industries. The main difference lies in terminology used by employers, but their responsibilities, work environment, and required certifications are very similar.

What are popular job titles related to Contract Drug Safety Associate jobs in Raleigh, NC?

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

What job categories do people searching Contract Drug Safety Associate jobs in Raleigh, NC look for?

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

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

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

Contract Drug Safety Associate jobs near you
Infographic showing various Contract Drug Safety Associate job openings in Raleigh, NC as of August 2026, with employment types broken down into 50% Full Time, 25% Part Time, 8% Temporary, and 17% Contract. Highlights an 100% In-person job distribution, with an average salary of $99,363 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

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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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