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Safety Scientist Jobs in Raleigh, NC (NOW HIRING)

Drug Safety Coordinator

Clayton, NC ยท On-site

$19.23 - $26/hr

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 ...

New

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 ...

New

Lead Exposure Data Scientist

Morrisville, NC ยท On-site

$120 - $180/hr

The Lead Exposure Data Scientist will be responsible for assisting in the development and ... We identify critical safety and sustainability issues, asking the tough questions because we ...

New

Follow safety rules, guidelines and standards for all projects. Participate in pre-task planning ... Proficient scientific professional responsible for conducting site testing and making ...

Follow safety rules, guidelines and standards for all projects. Participate in pre-task planning ... Proficient scientific professional responsible for conducting site testing and making ...

Report any safety issues or concerns to management. * Provide and lead continuous quality ... Career level, fully competent scientific professional responsible for planning, scheduling ...

Report any safety issues or concerns to management. * Provide and lead continuous quality ... Career level, fully competent scientific professional responsible for planning, scheduling ...

Environmental Scientist

Durham, NC ยท Hybrid

$72K - $95K/yr

Join our team of innovative and passionate professionals where we embrace a culture of safety ... Ideal candidates will have a Bachelor of Science degree in biology, biological sciences, ecology ...

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Safety Scientist information

See Raleigh, NC salary details

$29

$59

$89

How much do safety scientist jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for safety scientist in Raleigh, NC is $59.70, according to ZipRecruiter salary data. Most workers in this role earn between $41.35 and $71.73 per hour, depending on experience, location, and employer.

How does a safety scientist typically collaborate with other departments to ensure drug safety throughout a product's lifecycle?

A Safety Scientist works closely with clinical development, regulatory affairs, and medical teams to monitor and assess the safety profile of pharmaceutical products. They regularly participate in cross-functional meetings, review safety data from clinical trials or post-marketing sources, and communicate findings to internal and external stakeholders. This collaborative approach ensures that potential risks are identified early and that appropriate risk mitigation strategies are implemented and documented throughout the product's lifecycle.

What is a safety scientist?

Safety Scientists are professionals who monitor, assess, and manage the safety of pharmaceuticals, medical devices, or other products to ensure they do not pose undue risks to patients or consumers. They analyze data from clinical trials, post-marketing reports, and scientific literature to identify potential safety concerns. Additionally, Safety Scientists help develop risk management strategies and communicate findings to regulatory authorities and stakeholders.

What are the key skills and qualifications needed to thrive as a safety scientist?

To thrive as a Safety Scientist, you need a strong background in pharmacovigilance, drug safety regulations, and data analysis, typically supported by a degree in life sciences or a related field. Familiarity with safety databases (such as Argus or ARISg), signal detection tools, and compliance standards like GVP or FDA regulations is crucial. Strong attention to detail, analytical thinking, and effective communication are essential soft skills for assessing risks and collaborating with cross-functional teams. These skills ensure accurate safety assessments, regulatory compliance, and the protection of patient wellbeing throughout the drug lifecycle.

What is the difference between Safety Scientist vs Safety Engineer?

AspectSafety Scientist
Required Credentials
Bachelor's or higher in safety, environmental science, or related field; certifications like ASP or CSP often preferred
Work Environment
Research labs, corporate safety departments, or regulatory agencies
Employer & Industry Usage
Used across manufacturing, healthcare, and chemical industries focusing on safety research and policy development
Comparison Summary

Safety Scientists focus on researching and developing safety protocols, policies, and compliance strategies, often working in labs or policy settings. Safety Engineers, on the other hand, are more involved in designing and implementing safety systems on the ground, such as safety equipment and procedures. Both roles require safety certifications and work within similar industries, but Safety Scientists emphasize research and policy, while Safety Engineers focus on practical safety system implementation.

What job categories do people searching Safety Scientist jobs in Raleigh, NC look for? The top searched job categories for Safety Scientist jobs in Raleigh, NC are:
Infographic showing various Safety Scientist job openings in Raleigh, NC 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 $124,179 per year, or $59.7 per hour.

Drug Safety Coordinator

Belcan

Clayton, NC โ€ข On-site

$19.23 - $26/hr

Contractor

This job post hasย expired 1 day ago.ย Applications are no longer accepted.


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