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Entry Level Drug Safety Associate Jobs in Raleigh, NC

Belcan

Drug Safety Coordinator

Clayton, NC

$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 ...

SUPPLY.com

Warehouse Associate - Entry Level

Garner, NC · On-site

$14.25 - $17/hr

Ferguson is currently seeking an entry level Warehouse Associate to join our team! Schedule: Monday ... Knowledge of safety regulations and procedures. *Pre-employment drug and background screening ...

HP Products

Warehouse Associate - Entry Level

Garner, NC · On-site

$14.25 - $17/hr

Ferguson is currently seeking an entry level Warehouse Associate to join our team! Schedule: Monday ... Knowledge of safety regulations and procedures. *Pre-employment drug and background screening ...

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Entry Level Drug Safety Associate information

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$11

$47

$83

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

As of Aug 25, 2026, the average hourly pay for entry level 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 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 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 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.

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.

How much does an entry level drug safety associate make in the US?

An entry-level drug safety associate in the US typically earns between $50,000 and $70,000 annually, depending on location, education, and company size. Starting salaries may be lower but can increase with experience and additional certifications in pharmacovigilance or related fields.

How to become an entry level drug safety associate?

To become an entry-level drug safety associate, candidates typically need a bachelor's degree in life sciences, pharmacy, or a related field. Relevant skills include attention to detail, knowledge of pharmacovigilance processes, and familiarity with safety databases; certifications like the Drug Safety Certification can enhance prospects. Prior internship or related experience can also be beneficial for entry into this role.

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

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

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

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

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

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

Entry Level Drug Safety Associate jobs near you
Infographic showing various Entry Level Drug Safety Associate 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 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $99,363 per year, or $47.8 per hour.

Drug Safety Coordinator

Clayton, NC

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

$19.23 - $26/hr

Full-time

Posted 19 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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