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Scientific Affairs Manager Jobs in Raleigh, NC (NOW HIRING)

Osv_bioventus

Regulatory Affairs Manager

Durham, NC · On-site

The Regulatory Affairs Manager is responsible for developing and executing global regulatory ... Bachelor's degree required (study area in Engineering or life sciences preferred, but other degrees ...

Bioventus

Regulatory Affairs Manager

Durham, NC · On-site

The Regulatory Affairs Manager is responsible for developing and executing global regulatory ... Bachelor's degree required (study area in Engineering or life sciences preferred, but other degrees ...

Osv_bioventus

Regulatory Affairs Manager

Durham, NC

The Regulatory Affairs Manager is responsible for developing and executing global regulatory ... Bachelor's degree required (study area in Engineering or life sciences preferred, but other degrees ...

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How much do scientific affairs manager jobs pay per hour?

As of May 28, 2026, the average hourly pay for scientific affairs manager in Raleigh, NC is $43.90, according to ZipRecruiter salary data. Most workers in this role earn between $39.23 and $52.36 per hour, depending on experience, location, and employer.

What Does a Scientific Affairs Manager Do?

As a scientific affairs manager, you oversee informational communications for a medical or scientific research company, such as a pharmaceutical development firm or a scientific professional society. Your responsibilities include maintaining websites and other informational resources about clinical studies, lab news, and research breakthroughs. You may also help develop public education programs, coordinate conferences or other events, and maintain membership databases. In addition to your communications duties, you may seek financial and institutional support for your organization and respond to public inquiries about its research and objectives.

What are the key skills and qualifications needed to thrive as a Scientific Affairs Manager, and why are they important?

To thrive as a Scientific Affairs Manager, you need a strong background in life sciences or a related field, often supported by an advanced degree (e.g., PhD, PharmD) and experience in medical writing or regulatory affairs. Familiarity with regulatory submission systems, scientific literature databases, and compliance standards like GxP is typically required. Excellent communication, project management, and stakeholder engagement skills are vital for collaborating across departments and with external partners. These competencies ensure accurate scientific communication, regulatory compliance, and effective support of product development and commercialization.

How does a Scientific Affairs Manager typically collaborate with cross-functional teams within an organization?

A Scientific Affairs Manager works closely with various departments such as regulatory affairs, clinical development, marketing, and medical affairs to ensure that scientific information is accurately communicated and that product strategies align with scientific evidence. They often serve as the scientific bridge between internal teams and external stakeholders, including healthcare professionals and regulatory agencies. This role involves facilitating knowledge sharing, supporting the development of scientific materials, and ensuring compliance with industry standards. Effective collaboration is key to driving informed decision-making and advancing organizational goals.

What are Scientific Affairs Managers?

Scientific Affairs Managers are professionals responsible for bridging the gap between scientific research and business objectives within organizations, particularly in industries like pharmaceuticals, biotechnology, and healthcare. They oversee scientific communications, manage regulatory compliance, and ensure that products or research findings are accurately and effectively communicated to regulatory bodies, healthcare professionals, and other stakeholders. Their role often involves collaborating with research teams, marketing departments, and regulatory agencies to support the development and approval of new products. Scientific Affairs Managers play a crucial role in ensuring that scientific information is clear, accurate, and aligned with both business goals and regulatory standards.

What is the difference between Scientific Affairs Manager vs Medical Science Liaison?

AspectScientific Affairs ManagerMedical Science Liaison
Required credentialsAdvanced degree (PhD, PharmD, MD)Advanced degree (PhD, PharmD, MD)
Work environmentCorporate, research, and development teamsMedical and clinical settings, healthcare providers
Employer and industry usagePharmaceutical, biotech companiesPharmaceutical, biotech, medical device companies
Common search and comparison intentUnderstanding roles in scientific communication and strategyClarifying clinical and medical information dissemination

The Scientific Affairs Manager and Medical Science Liaison roles both require advanced degrees and work within pharmaceutical and biotech industries. While the Scientific Affairs Manager focuses on strategic scientific communication and regulatory support within companies, the Medical Science Liaison primarily engages with healthcare professionals to share clinical data. Both roles are vital for bridging scientific research and medical practice but differ in their daily interactions and focus areas.

More about Scientific Affairs Manager jobs
What are the most commonly searched types of Scientific Affairs jobs in Raleigh, NC? The most popular types of Scientific Affairs jobs in Raleigh, NC are:
What are popular job titles related to Scientific Affairs Manager jobs in Raleigh, NC? For Scientific Affairs Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Scientific Affairs Manager jobs in Raleigh, NC look for? The top searched job categories for Scientific Affairs Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Scientific Affairs Manager jobs? Cities near Raleigh, NC with the most Scientific Affairs Manager job openings:
Scientific Affairs Manager jobs near you
Regulatory Affairs Manager

Regulatory Affairs Manager

Tunnell Consulting

Raleigh, NC • On-site

Full-time

Posted 13 days ago

Job description

Tunnell Consulting is an employee-owned, life sciences management consulting firm. Known for solving complex problems in the life sciences, we support the mission and objectives of a variety organizations including biotech, pharma, the U.S. Government, foundations, public/private partnerships, investors, and emerging companies. The variety of clients and issues that we support give our team and our organization an ever-increasing breadth of experience to add to our deep industry and functional expertise. Headquartered in the Philadelphia area, we also have a presence in Washington DC, and Boston.
One of our clients' is seeking a Regulatory Affairs Subject Matter Expert (SME) with deep experience in soft gelatin (softgel) dosage forms to lead regulatory strategy and compliance activities. This role will support product development, commercialization, and lifecycle management across global markets. This is a remote project estimated for 6 months to support two sites, one based in North Carolina and the other in the Netherlands. Hours are estimated to be 20-40 hours/week.
In this role, you will serve as a key regulatory advisor, ensuring products meet all applicable requirements for dietary supplements, OTC, or pharmaceutical products, with a strong focus on labeling, claims, and manufacturing compliance.
Title: Sr. Regulatory Affairs Manager
Responsibilities Include
  • Serve as the Sr Regulatory Affairs Manager for soft gelatin (softgel) formulations and manufacturing operations
  • Develop and execute regulatory strategies to support product development, commercialization, and lifecycle management activities
  • Ensure compliance with U.S. FDA and global regulatory requirements (e.g., 21 CFR Part 111/210/211, labeling regulations) and post-approval change management expectations
  • Review and approve product labels, claims, and marketing materials for regulatory compliance
  • Support product registrations, submissions, and ongoing lifecycle management activities
  • Partner cross-functionally with R&D, Quality, and Manufacturing to ensure regulatory alignment throughout development
  • Assess regulatory impact of deviations, CAPAs, change controls, and manufacturing changes
  • Provide regulatory guidance on formulation changes, manufacturing process updates, technical transfers, and global market entry
  • Monitor and interpret regulatory changes and communicate impact to stakeholders
  • Support audits, inspections, and regulatory inquiries
  • Maintain accurate regulatory documentation and ensure audit readiness

Experience/Education
  • Bachelor's degree in a scientific, regulatory, or related field (advanced degree preferred)
  • 8+ years of Regulatory Affairs experience in pharma, biotech, or dietary supplements
  • Strong expertise in soft gelatin (softgel) dosage forms required
  • Deep knowledge of U.S. FDA regulations and relevant global requirements
  • Experience with labeling, claims review, and compliance (supplements or OTC preferred)
  • Familiarity with cGMP and manufacturing processes
  • Proven ability to work cross-functionally and influence stakeholders
  • Strong communication, analytical, and problem-solving skills

Tunnell strives to hire and retain the most qualified talent. We believe that having employees with different backgrounds and capabilities contributes to the success of our business. To attract qualified applicants, Tunnell posts to a wide variety of job sites. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Please be advised that certain client contracts may outline specific requirements for onsite work. Tunnell employees and/or contractors are expected to comply with all client requirements, including any safety and health protocols.

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