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

Position Summary The School Safety Coordinator is responsible for developing, implementing, and ... Employees in this position are subject to drug and alcohol testing in accordance with Thales' Drug ...

Position Summary The School Safety Coordinator is responsible for developing, implementing, and ... Employees in this position are subject to drug and alcohol testing in accordance with Thales' Drug ...

We know our associates are our best asset. Therefore, we invest in our associates by providing ... Must comply with the company's drug and alcohol testing requirements and background screening ...

We know our associates are our best asset. Therefore, we invest in our associates by providing ... Must comply with the company's drug and alcohol testing requirements and background screening ...

We know our associates are our best asset. Therefore, we invest in our associates by providing ... Must comply with the company's drug and alcohol testing requirements and background screening ...

Corporate Safety & Risk Specialist

Apex, NC · On-site

$80K - $100K/yr

CFE, Inc. is a drug-free workplace. All employment offers are contingent on: * Pre-employment drug screening * Completion of a Post-Offer Medical Questionnaire Ready to make a difference in safety ...

Corporate Safety & Risk Specialist

Apex, NC · On-site

$80K - $100K/yr

CFE, Inc. is a drug-free workplace. All employment offers are contingent on: * Pre-employment drug screening * Completion of a Post-Offer Medical Questionnaire Ready to make a difference in safety ...

Safety Officer*

NC · On-site

$65K - $86K/yr

Additionally, this role will oversee the County's ADA program, MVR program, Drug and Alcohol ... Associate Risk Management (ARM) Certified Risk Manager (CRM) Certified Safety Professional (CSP ...

Showing results 41-60

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.

What are the most commonly searched types of Drug Safety jobs in Raleigh, NC?

The most popular types of Drug Safety 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:

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.

Manufacturing Associate, Bulk Drug Substance Upstream - Days

Amgen

Holly Springs, NC

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 26 days ago


Job description

Career CategoryManufacturingJob Description

HOWMIGHT YOU DEFY IMAGINATION?

You'veworked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills,experienceand passion to work toward your goals? At Amgen, our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies, reaching over10 million patientsworldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the AmgenFleXBatch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. TheFleXBatch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.

Manufacturing Associate, Bulk Drug Substance Upstream - Days

Live

What you will do

Let'sdo this!Let'schange the world! In this dynamic role, you will be an Associate in the manufacturing organization at Amgen North Carolina (ANC). The scheduleisa rotating 2-2-3,5:45AM-6:15PM(12-hour shift).Associates will be completing operations on the floor inourupstreamareaandare responsible forthe manufacturing of cGMP (Current Good Manufacturing Practices) drugsubstance.

With general direction, the Associate will support all floor operationsin accordance withcGMPpractices.

Responsibilities will include...

Compliance:

  • Completes workin accordance withestablished cGMP procedures and policies (Standard Operating Procedures [SOPs], Manufacturing Procedures [MPs], Job Hazard Analysis [JHAs], Code of Federal Regulations [CFR]) with strict adherence to safety and compliance

  • Assure proper gowning and aseptic techniques are always followed

Process/Equipment/Facilities:

  • Perform hands-on operations including set-up, cleaning, sanitization,monitoringof equipment and assigned area

  • Run andmonitorcritical process tasks per assigned procedures

  • Perform in-process sampling,operateanalytical equipment, and complete process documentation (Electronic Batch Records [EBRs])

  • Identifyand escalate issues and concernsregardingdaily routine functions related to process and tasks; may engage with team on potential solutions

  • Perform documentation for assigned functions (i.e., equipment logs, EBRs)

  • Collaborate as part of a cross-functional team (i.e., QA/QC, F&E (Facilities & Engineering), PPIC, Mfg., PD (Process Development), Regulatory, etc.) in completing production activities

  • Maintain an organized, clean, and workable space

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The hard-working professionals weseekare team players with these qualifications.

Basic Qualifications:

  • High School/GED + 2 years manufacturing and/or other regulated environment experience

Or

  • Associate's Degree+ 6 months manufacturing and/or other regulated environment experience

Or

  • Bachelor's Degree

Preferred Qualifications:

  • Completion of NCBioWorksCertification Program

  • Experience in a regulated industry such as biotechnology or pharmaceutical

  • Basic understanding and process experience in a cGMP manufacturing facility

  • Excellent verbal and written communication

  • Proficient Microsoft Office skills, and knowledge of other electronic systems such as EBR/MES, Delta V, and Electronic Quality Systems

  • An ability todemonstratedesire and drive to learn and grow their understanding of operations and processes

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth and well-being.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

Amgen offers a Total Rewards Plancomprisinghealth and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

  • Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.

  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan

  • Stock-based long-term incentives

  • Award-winning time-off plans and bi-annual company-wide shutdowns

  • Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

#AmgenNorthCarolina

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation toparticipatein the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

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Salary Range

70,985.20USD -96,038.80USD