Pharmacovigilance Jobs at Azurity Pharmaceuticals | Raleigh, NC | APPLY NOW
Looking for rewarding pharmacovigilance jobs in the pharmaceutical industry? Azurity Pharmaceuticals in Raleigh, NC is hiring a Drug Safety Associate to join its Medical Affairs team. Pharmacovigilance Jobs provide hands-on experience in patient safety, FDA compliance, and clinical trial support. If you’re seeking impactful pharma jobs that advance your career, this opportunity lets you grow with a leading specialty pharmaceutical company.
Job Position: Drug Safety Associate
Location: Raleigh, NC
About the Company:
Azurity Pharmaceuticals is a privately held specialty pharmaceutical company dedicated to developing innovative, high-quality medications for underserved patients. With products spanning cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, Azurity has positively impacted millions of patients. The company combines integrated capabilities with a strong partner network to continuously expand its product portfolio and late-stage pipeline.
About the Role:
The Medical Affairs team at Azurity is seeking a motivated Drug Safety Associate to support pharmacovigilance jobs across the organization. Reporting to the Director of Drug Safety, this role ensures compliance with FDA regulations, manages safety data, and supports ongoing drug safety initiatives.
Key Responsibilities: Pharmacovigilance Job
- Maintain compliance with PV activities per SOPs and FDA regulations.
- Assist in safety agreement editing, renewal tracking, and formatting.
- Manage safety-related information and support case reviews for clinical trials.
- Handle safety email systems, partner reconciliations, and cross-functional communication.
- Contribute to safety reports including PADERs and PSURs.
- Organize and author SOPs, safety reports, and internal project management tools.
- Maintain audit-ready electronic files and ensure data completeness.
- Assist in developing safety-related training materials and collaborate with other departments for timely report submissions.
Qualifications and Education Requirements:
- Bachelor’s or Master’s degree in Life Sciences, Healthcare, or equivalent experience.
- Minimum 3 years experience reviewing individual case reports, literature, and aggregate reports.
- Knowledge of MedDRA coding, FDA regulations, and safety databases.
- Strong analytical, problem-solving, and communication skills.
- Proficiency in Microsoft Office and Adobe Acrobat.
- Ability to thrive independently and collaboratively in a fast-paced, hybrid work environment.
Physical & Mental Requirements: Pharma Job Consideration
- Must be able to sit for long periods and occasionally lift up to 25 lbs.
- Frequent walking, sitting, talking, and using computers or handheld devices.
- Reasonable accommodations available for individuals with disabilities.
Benefits of Pharmacovigilance Jobs:
- Competitive compensation with annual performance-based bonuses.
- Comprehensive health coverage including medical, dental, and vision insurance.
- Hybrid work model – 2 days remote, 3 days in-office.
- 401(k) plan with dollar-for-dollar matching up to 5%.
- Generous PTO – 15 vacation days + 5 sick/wellness days.
- 13 paid holidays plus an extra week off during Christmas/New Year.
- Tuition reimbursement for professional courses and certifications.
- Peer recognition platform – Azurity High Five to celebrate achievements.
