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

Job Title: Drug Safety Associate

***Hybrid- Position Located in Clayton, NC***

Job Description

The Drug Safety Associate serves as an independent contributor within a global drug safety and pharmacovigilance team, efficiently and effectively completing drug safety tasks and deliverables with minimal oversight. In this role, you obtain and process adverse event data to ensure strict adherence to Good Clinical Practices (GCP), regulatory guidelines, and standard operating procedures, while supporting a collaborative team environment across clinical, scientific, and operational functions.

Responsibilities

• Monitor all incoming information to identify potential adverse event (AE) data and ensure timely and accurate processing.
• Assemble relevant adverse event data for team meetings and ongoing safety evaluations.
• Enter adverse event reports into the tracking log, determine whether they are initial, follow-up, or duplicate reports, and create appropriate case folders.
• Review source documents to identify and remove all confidential patient information before further processing.
• Record protocol numbers and site/patient identifiers, when applicable, on all source documents to ensure accurate traceability.
• Provide completed adverse event reports and associated documentation to the designated case owner for further assessment and action.
• Serve as the first reviewer of source documents for adverse event reports within Global Pharmacovigilance, making the initial determination of report completeness.
• Identify the need for follow-up with reporters when information is incomplete or unclear, and initiate or support follow-up activities as appropriate.
• Maintain a basic understanding of clinical study protocols and scope of work to ensure accurate interpretation of adverse event information.
• Maintain a thorough understanding and strict adherence to GCP guidelines and regulatory reporting requirements for adverse events.
• Manage the receipt, review, and filing of literature sources that may contain adverse event information, ensuring that all relevant data are captured and processed.
• Collaborate with Drug Safety Scientists and leadership to foster a strong team environment among drug safety staff and across other departments.
• Demonstrate strong computer literacy and use safety databases, including ARGUS or similar systems, to support efficient case management and documentation.
• Prioritize and organize multiple tasks simultaneously, ensuring that drug safety deliverables are completed accurately and within required timelines.

Essential Skills

• Excellent technical skills, including the ability to comprehend and integrate scientific data from a variety of sources.
• Comprehensive knowledge of medical terminology to accurately interpret and process clinical and safety information.
• Strong interpersonal skills to work effectively with clinical, scientific, and operational stakeholders.
• Excellent organizational and prioritization skills to manage multiple cases and tasks concurrently.
• High degree of flexibility and the ability to multitask in a dynamic, fast-paced environment.
• Strong computer literacy, including proficiency with safety databases and standard office software.
• Ability to work as an independent contributor, efficiently and effectively accomplishing drug safety tasks with minimal oversight.
• 2–3 years of recent experience in a clinical setting or equivalent experience or training.
• Exposure to or experience in clinical drug development, preferably within a pharmacovigilance or drug safety context.

Additional Skills & Qualifications

• Associate degree in a relevant scientific, healthcare, or technical discipline.
• Experience with ARGUS or other safety database systems is preferred.
• Basic understanding of clinical study protocols and scopes of work.
• Background in drug safety or pharmacovigilance is highly beneficial.
• Ability to contribute to a collaborative, innovation-driven environment and participate in cross-functional projects.
• Interest in ongoing professional growth through continuous learning and exposure to advanced biopharma and plasma-based technologies.

Work Environment

This position operates in a hybrid work environment, combining remote work with on-site presence at a cutting-edge facility in the Durham area. The setting offers access to advanced biopharma and plasma-based technologies and is embedded within a vibrant biotech ecosystem. You will work in a mission-driven organization focused on supporting life-saving therapies and improving patient outcomes worldwide. The culture emphasizes collaboration across clinical, scientific, and operational teams, with supportive leadership that values expertise, transparency, and consultant contributions. Team members benefit from professional growth opportunities through cross-functional projects, continuous learning, and engagement with the broader Research Triangle talent network and quality of life. The environment is innovation-driven, stable, and growth-oriented, enabling you to do meaningful work and expand your skill set while contributing to a purpose that truly matters.

This is a Contract position based out of Raleigh, NC.

The pay range for this position is $19.23 - $26.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

This is a hybrid position in Raleigh,NC.

This position is anticipated to close on Aug 18, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.