Associate Director Field Medical Affairs Jobs in North Carolina
Associate Director Field Medical Affairs jobs in North Carolina represent one of the more active markets in the Southeast, concentrated in pharmaceutical, biotech, and medical device companies anchored across the Research Triangle and Charlotte corridor. Major employers including Novo Nordisk, Syneos Health, and Pfizer maintain significant North Carolina operations and hire regularly at this director level. Demand is strongest in oncology, rare disease, and cardiovascular therapeutic areas. Scan the live roles below and apply to whichever ones fit.
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INTRODUCTION
Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.
ROLE AND RESPONSIBILITIES
Brief team/department description: As part of the Regulatory Affairs team at Azurity, the Regulatory Affairs Associate/Senior Associate will assist in preparing, review and submission regulatory filings to the FDA and other global health agencies. The person will play crucial role in managing lifecycle of IND, NDA, ANDA, etc. The Regulatory Affairs Associate/Senior Associate will report to the Associate Director, Regulatory Affairs and will work cross-functionally with other Azurity teams including but not limited to Technical Operation, Quality Assurance, Clinical Development, Medical Affairs.
Principle Responsibilities:
- Provide regulatory assistance with due diligence requests to support new business development activities.
- Support interaction with FDA and other regulatory agencies for assigned commercial products.
- Assist in compiling and authoring regulatory filings (IND, NDA, ANDA, etc.) and post marketing supplements for assigned products.
- Manage the timelines associated with regulatory submissions such as post-marketing periodic reports.
- Manage archival of regulatory submissions, regulatory correspondence and associated logs and tracking mechanisms.
- Provide regulatory guidance on requirements for post-approval changes, as required, for assigned products.
- Review and provide regulatory assessments for change control documentation.
- Provide regulatory support to regulatory leadership meetings and presentations.
- Keep abreast of current regulations and regulatory guidance, assessing impact to assigned products and internal processes.
- Participate in various activities of setting goals, tracking deliverables and process improvements within the regulatory department.
- Other duties as assigned.
BASIC QUALIFICATIONS
- Minimum of Bachelor of Science or preferred advanced health care discipline degree (PharmD, PhD, Master of Science, etc.) or equivalent qualification.
- Minimum of 3 years in the pharmaceutical industry with at least 1 of those years in regulatory affairs.
- Combination of education and applicable job experience may be considered.
- Excellent organizational, interpersonal, verbal, and written communication skills, strong grammar, and proofreading/editing skills, and MS Office skills are required.
- Ability to work independently with minimal supervision in a fast-paced deadline driven environment.
- Keen attention to detail.
- Ability to rapidly adapt to changing environment and circumstances requiring flexibility, tolerance and great sense of urgency while ensuring that all cGMP and regulatory requirements are met.
- Ability to successfully communicate, negotiate and influence regulatory strategy to key stakeholders.
PHYSICAL & MENTAL REQUIREMENTS
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- Must be able to sit for long periods of time.
- While performing the duties of this job, the employee is frequently required to stand; walk; sit; talk and/or hear.
- May occasionally climb stairs and/or ride elevators.
- The employee must occasionally lift and/or move up to 25 pounds.
- Employee must be able to manipulate keyboard, operate a telephone and hand-held devices.
- Other miscellaneous job duties as required.
BENEFITS WE OFFER
- Unlock Your Earning Potential: Join our team and be rewarded with a competitive compensation package, including an annual bonus based on company performance, that recognizes your exceptional talent.
- Sales - In lieu of annual bonuses, we offer an Incentive compensation program that allows you to earn more - even over plan.
- Fuel Your Success: Sales Only - We understand the value of your hard work and provide a car reimbursement program and gas card for both business and personal use as part of our commitment to supporting you.
- Comprehensive Health Coverage: We value your well-being and offer excellent medical, dental, vision, and prescription coverage to ensure you and your family are always taken care of.
- Flexibility for Your Lifestyle: Achieve work-life balance with our hybrid work model, allowing you to work two days from home and three days in the office. Excludes Sales, Manufacturing, and some Operations positions.
- Invest in Your Future: Our Retirement Savings Plan (401K) is designed to help you secure a comfortable retirement by matching dollar for dollar up to 5%.
- Time Off That Counts: Take advantage of our generous time off policy, which offers up to 15 vacation days annually + rollover (up to 40 hours) as well as five sick/wellness days. For new employees, vacation accrual will be prorated based on your start date.
- Meaningful Time with Your Loved Ones: We close between Christmas and New Year’s to give you an extra week off to spend quality time with your family and recharge.
- Enjoy the Holidays: Over the course of the year, Azurity recognizes 13 holidays.
- Invest in Your Education: We support your professional growth with tuition reimbursement for undergraduate and graduate level courses or certifications.
- Recognize and Be Recognized: Our Azurity High Five peer recognition platform allows you to celebrate your colleagues' accomplishments and receive recognition for your own outstanding work.
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See All 35 Associate Director Field Medical Affairs Jobs in North Carolina
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Find JobsAssociate Director Field Medical Affairs Jobs by City in North Carolina
Where North Carolina roles are concentrated, by current openings.
Associate Director Field Medical Affairs Job Market in North Carolina
A snapshot from current North Carolina openings, updated as new roles post.
Who's Hiring



Top Industries Hiring
- Medical Devices
- Healthcare & Medical Services
- Biotechnology & Pharmaceuticals
- Education
- Manufacturing
What North Carolina Employers Look For
The qualifications that appear most often in associate director field medical affairs jobs across North Carolina.
- Advanced degree such as PharmD, MD, or PhD in a life sciences field required
- Minimum of five years medical affairs or clinical experience in the pharmaceutical or biotech industry
- Demonstrated experience leading or managing field medical science liaison teams
- Deep therapeutic area expertise in oncology, rare disease, or cardiovascular medicine preferred
- Strong record of cross-functional collaboration with clinical, regulatory, and commercial teams
- Excellent communication skills for scientific exchange with key opinion leaders and healthcare providers
Associate Director Field Medical Affairs Jobs in North Carolina: Frequently Asked Questions
How do you become an associate director field medical affairs in North Carolina?
Most associate director field medical affairs roles in North Carolina require an advanced clinical or scientific degree, typically a PharmD, MD, or PhD, combined with several years of field medical or medical science liaison experience. North Carolina does not have a state-issued license specific to medical affairs, but candidates in regulated therapeutic areas often hold active state pharmacy or clinical licensure through the North Carolina Board of Pharmacy or applicable licensing board. Experience managing MSL teams and demonstrated scientific communication skills are the clearest differentiators in the North Carolina hiring market.
Which companies hire associate director field medical affairss in North Carolina?
North Carolina associate director field medical affairs roles are posted by Dentsply Sirona, Azurity Pharmaceuticals, and Grifols and others right now, based on current listings on Migrate Mate as of July 2026. The Research Triangle area in particular draws a dense concentration of pharmaceutical and biotech companies that hire at this level on a recurring basis.
Which North Carolina cities have the most associate director field medical affairs jobs?
Raleigh, Durham, and Charlotte account for the most associate director field medical affairs openings in North Carolina. The Research Triangle cities of Raleigh and Durham lead because of the dense cluster of pharmaceutical headquarters, biotech firms, and contract research organizations based there, while Charlotte draws openings from medical device and specialty pharma companies with regional offices in that metro.
Are there remote associate director field medical affairs jobs in North Carolina?
Yes, and more than many roles at this level, since medical affairs directors often coordinate field teams and manage scientific strategy rather than conduct in-person clinical work daily. About 58% of associate director field medical affairs openings tied to North Carolina are remote or hybrid as of July 2026, reflecting the field-based nature of much of this work. Strategic, cross-functional, and team leadership responsibilities are the functions most commonly performed remotely.
How can I get hired as an associate director field medical affairs in North Carolina with little or no experience?
The most realistic entry path is to build experience first as a medical science liaison at a pharmaceutical or biotech company with North Carolina operations, such as those concentrated in the Research Triangle Park area, then move into an associate director role after demonstrating regional leadership. Many larger employers based in Durham and Research Triangle Park hire MSLs without prior industry experience if candidates hold a clinical or scientific doctoral degree. Gaining a North Carolina pharmacy license or completing a postdoctoral fellowship at a UNC system institution also strengthens a candidate's profile considerably.
Where can I find and apply to associate director field medical affairs jobs in North Carolina?
You can find and apply to associate director field medical affairs jobs in North Carolina on Migrate Mate, which lists current openings in the state. Search the listings to find roles that match your therapeutic area expertise and experience level, then apply directly to the ones that fit.
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