270 Results for

Director Of Regulatory Affairs Jobs in North Carolina

Jobs

Raleigh, NC26 days ago

The individual will oversee or represent regulatory on global and certain regional PRC (Promotional Review Committee) teams, SRC (Scientific Review Committee) teams and must possess a thorough knowledge of regulations for medical affairs activities, advertisement and promotional compliance governing drugs, device, cosmetic, and combination products and the ability to translate regulatory requirements into decision-ready guidance for senior stakeholders. Lead the team within Global Regulatory Affairs that provides strategic regulatory expertise and guidance to global internal leaders and stakeholders regarding the marketing of products including review of advertising, promotional and other related materials to ensure compliance with applicable regulations and guidance documents.

Durham, NC30 days ago

Included among the necessary activities are: oversight of regulatory CRO activities, planning and leading: meetings with regulatory authorities, compilation and submission of high-quality INDs, CTAs, BLAs/MAAs, meeting packages, responses to requests for information, amendments, and required elements such as safety reports, annual reports. Lead the preparation of regulatory submissions, ensuring the planning, coordination, preparation, and review of all submissions to global regulatory authorities including INDs, CTAs, BLAs, MAAs, amendments, responses to information requests and questions, safety reports, and annual updates/DSURs for assigned projects.

Greensboro, NC30+ days ago

p>Position Summary:

The Director of Quality & Regulatory will work collaboratively with colleagues across the company, and with outside partners, to design and execute global strategies for Market America products, including regulatory and compliance efforts and maintenance.

Above moderate to high levels in reading comprehension, writing, and speaking in English; active listening; attention to detail; critical thinking; mathematics, creative problem solving; complex problem solving; and judgment.

New!

Morrisville, NC4 days ago

$203,000–$253,000 Per Year

The position leads a global organization through a team of managers and functional leaders and serves as a key partner to Regulatory Affairs, Quality, Supply Chain, Manufacturing, Information Technology, Commercial, and Executive Leadership teams to ensure regulatory compliance, support global market access, and enable business growth.

The Senior Director, Strategic Regulatory Affairs & UDI provides leadership and oversight for global regulatory operations, regulatory systems, unique device identification (UDI), regulatory data governance, import/export regulatory compliance support, and regional Regulatory Affairs and Quality functions.

Raleigh, NC21 days ago

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Development and implementation of clinical regulatory strategies and tactics,including but not limited to, Modeling Informed Drug Development (MIDD), real- world data (RWD)/real-world evidence (RWE), and meta-analysis, for pipeline and commercial assets,while considering FDA and other health authority clinical and regulatory requirements.

As a part of the Regulatory Affairs team at Azurity, the Regulatory Affairs Director – Clinical Strategy will conduct in depth analysis of regulatory and clinical information to develop complex strategies supporting potential drug products for development and commercial drug products for expansion of the Azurity portfolio of medications.

Raleigh, NC30+ days ago

p>Brief Team/Department Description:

As a part of the Regulatory Affairs team at Azurity, the Regulatory Affairs Director - Clinical Strategy will conduct in-depth analysis of regulatory and clinical information to develop complex strategies supporting potential drug products for development and commercial drug products for expansion of the Azurity portfolio of medications.

Principle Responsibilities:

• Development and implementation of clinical regulatory strategies and tactics, including but not limited to, Modeling Informed Drug Development (MIDD), real-world data (RWD)/real-world evidence (RWE), and meta-analysis, for pipeline and commercial assets, while considering FDA and other health authority clinical and regulatory requirements.

Durham, NC29 days ago

p>The company is seeking a Director or Senior Director of Regulatory Affairs — with the final title set according to the selected candidate's background — to help shape and steer the execution of worldwide regulatory strategy across assigned programs, keeping all work consistent with applicable national and regional requirements as well as internal policy.

Direct the assembly of regulatory filings, overseeing the planning, coordination, drafting, and review of every submission sent to health authorities worldwide — including INDs, CTAs, BLAs, MAAs, amendments, replies to questions and information requests, safety reports, and annual updates/DSURs for assigned projects.

NC30+ days ago

$175,000–$219,000 Per Year

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards.

Raleigh, NC30+ days ago

p>The Director, Regulatory Affairs - Chemistry, Manufacturing, and Controls (CMC) is a senior-level contractor role responsible for defining and executing global CMC regulatory strategies across Dyne's development programs, from early-stage development through commercialization and post-approval lifecycle management. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.

Durham, NC7 days ago

$138,750–$231,250 Per Year

This role will ensure the development of appropriate global and/or regional regulatory strategy(s) and their execution for assigned asset(s) consistent with Medicines Development Strategy /Integrated Asset plan to ensure the development program meets the needs of the key markets identified and the Medicines Profile. Work with the Early/Medicine Development Team (EDT/MDT) or GRL, to ensure a robust regulatory strategy is in place to support the development program to meet the needs of the key markets identified in the Integrated Asset plan and the Medicine Profile.

Morrisville, NC30+ days ago

The Associate Director Regulatory Affairs CMC possesses strong leadership skills, broad knowledge of multiple aspects of regulatory affairs beyond CMC, across all phases of drug development, and a deep understanding of global CMC regulations, including GMP and region-specific guidelines, especially as they relate to gene therapies. We leverage our proprietary computational engine, in-house manufacturing infrastructure, and integrated design platform to engineer technologies and therapeutics with the potential to transform the treatment of a broad universe of diseases of high unmet need, with a focus on metabolic disorders, neurology, and ophthalmology.

Research Triangle Park, NC30+ days ago

The Associate Director, Regulatory Affairs (CMC) possesses strong leadership skills, broad knowledge of multiple aspects of regulatory affairs (beyond CMC) across all phases of drug development, and a deep understanding of global CMC regulations, including GMP and region-specific guidelines, especially as they relate to gene therapies. We are proud to have been named Triangle Business Journal’s Life Sciences 2024 “Best Private Company to Work For,” recognized by Forbes as one of “America’s Best Startup Employers of 2024,” and honored as one of BioSpace’s “2025 Best Places to Work.”

Raleigh, NC30+ days ago

$176,000–$242,000 Per Year

Recruitment Fraud NoticeBaxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. May participate in potential and established third party efforts (i.e. Due diligence activities, joint ventures, etc.).May provide direct supervision of individuals including mentoring, performance management and staffing decisions.

Winston Salem, NC30+ days ago

$10–$13 Per Year

Section Chief, Comparative Medicine and Vice Chair of Research Affairs - Academic Faculty mail to friend share to facebook share to twitter share to linkedin Apply Now Similar Jobs Vice Chair of Research Affairs and Section Chief of Comparative Medicine Department of Pathology Winston Salem, NC, United States Open Rank Tenure Track Position in Preclinical and Translational Musculoskeletal Research Winston Salem, NC, United States Research Faculty, Center for Sleep & Circadian Rhythms Winston Salem, NC, United States Musculoskeletal Researcher - Wake Forest Campus Winston Salem, NC, United States Academic Faculty - Cancer Biology Winston Salem, NC, United States Open Rank Academic Faculty - Child Health Outcomes Leader Winston Salem, NC, United States Program Manager II, Biostatistics and Data Science Winston Salem, NC, United States Open Rank Position (Tenured/Tenure Track) for Clinician Scientist in Alzheimer's Disease Winston Salem, NC, United States Open Rank Professor - Center for Remote Health Monitoring Winston Salem, NC, United States Program Director III, Oncology Clinical Trials Office, Atrium Health Levine Cancer Center Winston Salem, NC, United States Behavioral Health Continuing Education Coordinator Winston Salem, NC, United States Student Involvement and Community Engagement Coordinator Charlotte, NC, United States Ross Summer Student Research Intern - medical students only Charlotte, NC, United States Adjunct Faculty Math - Early College Charlotte, NC, United States Adjunct Faculty II - Math Early College Charlotte, NC, United States Intern - Senior Charlotte, NC, United States Instructor - Nursing Concord, NC, United States 314295 - Faculty I Nursing Education Charlotte, NC, United States Part-Time Clinical Faculty II Concord, NC, United States Clinical Faculty II Concord, NC, United States Simulated Participant Educator 318076 Charlotte, NC, United States facebook twitter linkedin instagram youtube My Account View All Jobs Teammates Site AtriumHealth.org

Join Our Talent Network Skip to main content Menu Search Jobs Search All Jobs Applicant Resources About Us Who We Are Compensation & Benefits Access and Opportunity Military Recruitment Events Talent Networks Featured Jobs Nursing Allied Health Administrative/Non-Clinical Leadership & Executive Browse All Opportunities Locations Alabama Charlotte Floyd Navicent Wake Forest Baptist Wake Forest University School of Medicine Physicians/APP Students Enter keyword, facility, job title, skills Enter City, State or Zip Back to Search Results Vice Chair of Research Affairs and Section Chief of Comparative Medicine Department of Pathology Winston Salem, NC, United States Job ID: R158581 Shift: Various Job Type: Regular Share: mail mail to friend share to facebook share to twitter share to linkedin Apply Now Department:85036 Wake Forest University Health Sciences - Academic Comparative MedicineStatus: Full timeBenefits Eligible:YesHours Per Week:40Schedule Details/Additional Information:VariesPay Range$0.00 - $0.00Vice Chair of Research Affairs and Section Chief of Comparative MedicineDepartment of PathologyThe RoleThe Department of Pathology at Wake Forest University School of Medicine (WFUSM) is seeking a dynamic, innovative and energetic leader to become the Vice Chair of Research Affairs and Section Chief of Comparative Medicine for the department.

NC30+ days ago

li>Provide regulatory support for assigned products/projects, coordinating cross-functional activities with various UTC product development groups (e.g., nonclinical, clinical, quality, marketing, safety, medical) to support execution of regulatory activities and adherence to established timelines.

The Regulatory Affairs Manager, Biologics/Senior Regulatory Affairs Manager, Biologics will lead regulatory activities for assigned existing and new programs, supporting product development from early development through post-approval.

New!

Raleigh, NC4 days ago

$260,000–$295,000 Per Year

li>Develop and foster strong collaborative relationships with internal partners, including Regulatory Affairs, Clinical Operations, Market Access, Medical Information, Pharmacovigilance, Sales and Marketing, Global product leadership, Global medical affairs, and clinical development, providing strategic medical insight and product/disease-state expertise to meet business objectives. Additionally, the Senior Medical Director will be a key contributor to the global life cycle management-led activities, including programs for future indications, cytokine testing, Investigator-Initiated Study strategy, and overall input into the creation and execution of product evidence generation plans.

North Carolina30+ days ago

For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram..

Collaborate with Medical Directors to conduct needs analysis to ensure training alignment with global and regional medical strategies and legal/compliance/regulatory requirements, and lead all medical training, including new hire training, virtual training, product and disease training, other skills training, and advanced training, training on new and existing initiatives and field materials, including internal journal clubs etc. and support any other business-need training.

NC30 days ago

$145,500–$205,000 Per Year

Bachelor's Degree in business, finance, life sciences, healthcare, information systems or related field with 12+ years of relevant experience in the life sciences industry (pharmaceutical, medical device or biotech) or, Master's Degree with 10+ years of relevant experience in the life sciences industry (pharmaceutical, medical device or biotech). The Associate Corporate Compliance Director reports to the Senior Corporate Compliance Director and serves as a key compliance business partner to Commercial and Medical Affairs, including Sales, Marketing, Commercial Training and Development, Patient Advocacy, and Medical Affairs.

Rtp, North Carolina30+ days ago

For additional information on Company benefits, please visit https://www.unither.com/careers/benefits-and-amenities .

Bachelor’s Degree in business, finance, life sciences, healthcare, information systems or related field with 12+ years of relevant experience in the life sciences industry (pharmaceutical, medical device or biotech) or,
Master’s Degree with 10+ years of relevant experience in the life sciences industry (pharmaceutical, medical device or biotech) .

Morrisville, NC30+ days ago

$224,000–$290,000 Per Year

li>Develop and foster strong collaborative relationships with internal partners, including Regulatory Affairs, Clinical Operations, Market Access, Medical Information, Pharmacovigilance, Sales, and Marketing, and provide medical insight and product- and disease-state expertise to meet business objectives.

Develop a US evidence generation strategy to address stakeholder (HCPs, payers, and patients) needs (including product differentiation, health outcomes), collaborating with HEOR and global partners.

New!

Charlotte, NC6 days ago

Remote

$100,000–$120,000 Per Year

p>With more than 135 years of history in healthcare education and as the largest nursing school in the country, Chamberlain University is committed to delivering a high-value education that prepares students to thrive as healthcare professionals. The College of Nursing offers a three-year Bachelor of Science in Nursing degree program and flexible post-licensure programs, such as the RN to BSN option, Master of Science in Nursing degree program, Doctor of Nursing Practice degree program and graduate certificates.

NC30+ days ago

For additional information on Company benefits, please visit https://www.unither.com/careers/benefits-and-amenities.

The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many others is an organ transplant, but only a small percentage of donated organs are available to address the vast need.

New!

Raleigh, NC4 days ago

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.

Raleigh, NC10 days ago

New!

Durham, NC4 days ago

ul>

Lead global regulatory strategy and product registration activities across North America, Europe, Latin America, and Asia-Pacific; oversee preparation, submission, and lifecycle management of regulatory dossiers (federal/state registrations, REACH, fertilizer/biostimulant regulations); ensure compliance with labeling, safety, environmental, and composition requirements; manage audits, inspections, and regulatory authority interactions for Biosciences and support these functions for traditional fertilizer.

The Director of Regulatory Affairs - Biological & Traditional Fertilizers, reporting to the Vice President of Product Innovation, leads the global regulatory strategy, registration, and compliance for a diverse portfolio of conventional fertilizer and biological products, ensuring full adherence to regulatory requirements while enabling innovation, speed to market, and sustained commercial growth.

High Point, NC30+ days ago

p>Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

High Point, NC30+ days ago

p>Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Charlotte, NC30+ days ago

Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands.

This role works closely with business partners for registrations in their respective countries to ensure compliance globally and acts as an internal champion for initiatives aimed at improving business systems and compliance.

NC30+ days ago

We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Working closely with cross-functional teams, you'll help develop and implement regulatory strategies that enable the successful commercialization of our advanced products, from initial planning through post-market activities.

Durham, NC30+ days ago

Works with stakeholders to serve as a point person for regulatory agency interactions, including preparation of briefing packages, including presentations, and strategy for meetings, and response to agency letters pertaining to assigned products.

Excellent written, verbal communication and presentation skills are required, including the ability to communicate clearly, concisely and effectively verbally and in writing.

Durham, NC12 days ago

Remote

$115,000–$130,000 Per Year

The Regulatory Affairs Project Manager will be responsible for developing and managing budgets, timelines, and quality guidelines for projects, thereby ensuring that expectations are met while identifying and mitigating risks.

University/college degree (life science preferred) or certification in a related allied health profession (i.e. nursing, medical or laboratory technology) from an appropriately accredited institution.

NC20 days ago

You will play a key leadership role in managing midsize to large Regulatory Affairs outsourcing programs, partnering closely with clients and cross-functional teams to drive operational excellence, ensure delivery against regulatory objectives, and support the successful progression of development and commercial programs.

Due to continued growth and the ongoing success of our Regulatory Affairs Consulting team, Parexel is seeking an experienced Senior Regulatory Affairs Consultant (Program / Client Partnership Manager) to join our team.

Durham, North Carolina12 days ago

Remote

$115,000–$130,000 Per Year

The Regulatory Affairs Project Manager will be responsible for developing and managing budgets, timelines, and quality guidelines for projects, thereby ensuring that expectations are met while identifying and mitigating risks.

University/college degree (life science preferred) or certification in a related allied health profession (i.e. nursing, medical or laboratory technology) from an appropriately accredited institution.

Raleigh, North Carolina17 days ago

li>

Contribute to at least two of the following areas: interactions with regulatory agencies, early phase consulting, development planning (PDP/RDP/CDP), scientific/agency advice, orphan drugs/pediatric development, medical devices.

Demonstrable experience within regulatory affairs, including development of regulatory strategies, document writing, marketing authorization applications, clinical trials, post-licensing activities, and direct regulatory agency interaction.

North Carolina21 days ago

Due to continued growth and the ongoing success of our Regulatory Affairs Consulting team, Parexel is seeking an experienced Senior Regulatory Affairs Consultant (Program / Client Partnership Manager) to join our team.

Clayton, NC24 days ago

p>Summary:

Implement worldwide regulatory product registration strategies, prepare complex registration dossiers, establish and maintain tracking of product registrations to determine what products can be shipped to intended markets in accordance with business plan with a specific focus on labeling, labeling requirements, and implementation.

Prepare complex registration dossiers, local application forms; negotiate documentation required for worldwide markets which may include product custom clearance documentation and coordinate with International Customer Service, Quality and Commercial preparation of required documentation in accordance with local requirements.

Wilmington, NC30+ days ago

Remote

$220,000–$300,000 Per Year

This leader owns the full licensing lifecycle -the GNF fuel facility, the installed base work on extended power uprates and fuels licensing, and new reactor deployment including initial commercial development, license applications, topical report, and multi-project commercial execution - while building a high-performing, accountable organization rooted in a strong nuclear safety culture and operational excellence.

The executive that leads the Regulatory Affairs & Licensing team drives the strategic vision and execution of global nuclear licensing and regulatory affairs, which includes directing the licensed activities supporting the installed base fuel & services business and accelerating the commercialization and deployment of next-generation technologies such as the BWRX-300 across North American and European markets.

Raleigh, North Carolina13 days ago

p>Company Profile: North Carolina’s Electric Cooperatives (http://ncemcs.com/about/ncemc.htm) is the brand for the family of organizations formed to support the state’s 26 local electric cooperatives, including: North Carolina Electric Membership Corporation, the power supplier to many of the electric cooperatives; North Carolina Association of Electric Cooperatives, the cooperatives’ trade association; and Tarheel Electric Membership Association, Inc. (TEMA), a central purchasing and materials-supply cooperative.

Summary Description: At North Carolina’s Electric Cooperatives you will be part of an exciting mission to build a Brighter Future for our state and rural communities, making a real difference in the lives of 2.8 million consumer members.

Durham, NC7 days ago

$113,850–$189,750 Per Year

GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment.

Morrisville, NC17 days ago

$150,000–$170,000 Per Year

p>The Real-World Science, Epidemiology and Scientific Affairs team focuses on generating real-world evidence and supports biopharmaceutical companies throughout the product lifecycle, from early pre-launch planning to launch, and post-marketing management.

Knowledge: Broad experience in quantitative methods in real-world evidence and health services research, with the focus on design of non-interventional studies and data analysis using observational retrospective and prospective data.

Greenville, NC30+ days ago

$77,000–$80,000 Per Year

p>Job Title Director of Admissions Brody School of Medicine Position Number 500255 Vacancy Open to All Candidates Department EHH BSOM Acad Aff Admissions Department Homepage https://medicine.ecu.edu/admissions/

Directs all aspects of admissions operations, including but not limited to program interface with: American Medical College Application Service (AMCAS), a combination of internal and national software programs for managing admissions data and application fees), the UNC System Residency Determinations Services, Certiphi (for criminal background checks).

Durham, NC30+ days ago

$61,535–$95,880 Per Year

ul>

Serve as administrative lead for the academic support program-administer and evaluate universal support programs; identify students needing individual support; coordinate with faculty offering academic support; and provide individual support for at-risk students.

Leaves of Absence, Transfers, and Visitors: Manage requests to visit away; provide advising for transfers and visitors; coordinate leave-related academic guidance with Student Affairs; ensure accurate information is maintained by the Registrar.

New!

Cary, NC3 days ago

Remote

They are known for delivering high-impact real-world evidence, economic modeling, and value strategy solutions that help biotech, pharma, and medical device companies secure market access and reimbursement. Were hiring for a Business Development Director to drive new business and expand client relationships within HEOR and market access services.

New!

NC5 days ago

The Associate Director plays a critical leadership role in advancing Davidson's residential experience by ensuring efficient, student-centered housing operations, facilities coordination, access management, occupancy processes, and service delivery for the College's residential population.

In collaboration with the Assistant Dean and Director, provide strategic oversight for housing-related customer service across Residence Life, including central office operations, student inquiries, parent/family questions, and campus partner communication.

Charlotte, NC30+ days ago

On Location Charlotte OfficeType of employment Permanent Full Time 40 hoursTHE ROLEReporting to the Head of Legal Corporate Legal Affairs &A the Director Legal Affairs - North American M&A will play a critical strategic role in supporting business development and growth across North America leading the legal function for mergers acquisitions joint ventures related strategic investments and North American capital markets activities. Oversee the coordination of due diligence and specialist advisory work including sector-specific regulatory and antitrust matters ensure timely progress transparency and issue escalation as needed efficiently advising business leaders on key transactional risks and mitigation strategies.

Greensboro, NC11 days ago

$111,182–$146,292 Per Year

p>The Successful Candidate:

Demonstrates unquestioned integrity and earns trust through consistent, principled decision-making - especially in complex or high-visibility situations;
Brings deep financial expertise and professional credibility, serving as a confident and knowledgeable resource to City Council and executive leadership;
Communicates with clarity and sound judgment, translating complex financial issues into practical guidance and informed decision-making;
Maintains precision and discipline in financial oversight while balancing long-term strategy with day-to-day operational realities;
Builds respectful partnerships across departments, supporting collaboration and strengthening organizational alignment;
Leads inclusively by directing, mentoring, and empowering a diverse, high-performing workforce while fostering collaboration, equity, and innovation;
Upholds Greensboro's values of being purpose-driven, people-centered, data-informed, resilient, and equitable in both leadership style and financial decision-making; and. The Deputy Finance Director provides oversight across six divisions: Accounting, Collections, Treasury Management, Financial Reporting, Purchasing Service, Centralized Contracting, and Equipment Services (Equipment Services manages, maintains, and repairs the 1,8000-piece automotive and rolling stock fleet used by City Departments).

Greensboro, NC21 days ago

$111,182–$146,292 Per Year

The Successful Candidate: Demonstrates unquestioned integrity and earns trust through consistent, principled decision-making - especially in complex or high-visibility situations; Brings deep financial expertise and professional credibility, serving as a confident and knowledgeable resource to City Council and executive leadership; Communicates with clarity and sound judgment, translating complex financial issues into practical guidance and informed decision-making; Maintains precision and discipline in financial oversight while balancing long-term strategy with day-to-day operational realities; Builds respectful partnerships across departments, supporting collaboration and strengthening organizational alignment; Leads inclusively by directing, mentoring, and empowering a diverse, high-performing workforce while fostering collaboration, equity, and innovation; Upholds Greensboro's values of being purpose-driven, people-centered, data-informed, resilient, and equitable in both leadership style and financial decision-making; and. The Deputy Finance Director provides oversight across six divisions: Accounting, Collections, Treasury Management, Financial Reporting, Purchasing Service, Centralized Contracting, and Equipment Services (Equipment Services manages, maintains, and repairs the 1,8000-piece automotive and rolling stock fleet used by City Departments).

Charlotte, NC30+ days ago

Reporting to the Vice President of Government Affairs, the Director will be responsible for executing government relations strategies, influencing key decision-makers, building durable relationships, and effectively communicating Progress' and/or the industry's positions before state and local governments, with limited federal engagement as needed.

Job Summary:

The Director of Government Relations will represent Progress Residential ("Progress") by advocating before state and local government officials on policies relevant to Progress Residential, its affiliates, Owners, and Property Managers in the Single-Family Rental ("SFR") industry.

Durham, NC30+ days ago

Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals: Licensed Physician (MD or DO) Completion of Internal Medicine or Family Medicine residency training 3 plus years of demonstrated expertise in Infectious Diseases, either patient care or research Drug development OR clinical trials experience Preferred Qualifications: If you have the following characteristics, it would be a plus: Either clinical fellowship in Infectious Diseases, in HIV and/or extensive experience in HIV clinical treatment and management Expertise in conducting clinical trials, including 2+ years in drug development and execution of trials in HIV or infectious diseases Proven leadership experience in matrix environments and team collaborations Active medical license or equivalent qualification to practice medicine Exceptional communication skills with the ability to foster strong professional relationships across functional areas and with external stakeholders #LI-ViiV #LI-GSK Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program ViiV offers US employees. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following… Clinical Trial Management and Oversight Serve as Clinical Trial Director for Phase 1-4 trials, designing study protocols and supplementary documentation, including study procedures manuals, analysis plans, and protocol deviation plans.

Greensboro, North Carolina30+ days ago

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Working at Guilford provides you with a rewarding opportunity to impact the developing lives of students from a range of diverse backgrounds.

People are drawn to Guilford College for a number of reasons, including the College’s Core Values of community, diversity, equality, excellence, integrity, justice, and stewardship.

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Director Of Regulatory Affairs Jobs in North Carolina

Senior Director, Advertising and Promotional Compliance Lead - Global Regulatory Affairs Merz North America Inc

Director (Senior Director), Regulatory Affairs Shattuck Labs Inc

Director of Quality Assurance and Regulatory Affairs Market America Inc

Sr. Director, Strategic Regulatory Affairs and UDI Teleflex Inc

Director, Regulatory Affairs – Clinical Strategy Azurity Pharmaceuticals - US

Director, Regulatory Affairs - Clinical Strategy Azurity Pharmaceuticals Inc

Senior/Director - Regulatory Affairs implaion

Director, Regulatory Affairs Thermo Fisher Scientific Inc

Director, Regulatory Affairs CMC ProPharma Group Holdings LLC

Associate Director Regulatory Affairs, Oncology GSK plc

Associate Director, Regulatory Affairs (CMC) Kriya Therapeutics Inc

Associate Director, Regulatory Affairs (CMC) Kriya Therapeutics

Associate Director, Regulatory Affairs Baxter International Inc

Vice Chair of Research Affairs and Section Chief of Comparative Medicine Department of Pathology Atrium Health

Regulatory Affairs Manager / Senior Regulatory Affairs Manager - Biologics United Therapeutics Corp

Senior Medical Director , US Immunology Medical Affairs Swedish Orphan Biovitrum AB

Assoc. Director, Medical Affairs Training BioCryst Pharmaceuticals

Associate Corporate Compliance Director - Commercial & Medical Affairs United Therapeutics Corp

Associate Corporate Compliance Director – Commercial & Medical Affairs United Therapeutics

Rheumatology (Senior) Medical Director - Medical Affairs Swedish Orphan Biovitrum AB

Dean of Academic Affairs, Charlotte Campus, Prelicensure BSN Nursing Covista Inc

Senior Medical Director - Medical Monitoring (Clinical & Medical Affairs) United Therapeutics Corp

Vice President, Global Head of Regulatory Affairs Azurity Pharmaceuticals - US

Vice President, Global Head of Regulatory Affairs Azurity Pharmaceuticals Inc

Director of Regulatory - Biological & Traditional Fertilizers The Mosaic Co

Sr. Regulatory Affairs Manager Validation & Engineering Group, Inc

Sr. Regulatory Affairs Manager Validation & Engineering Group

Regulatory Affairs Manager Dentsply Sirona Inc

Regulatory Affairs Manager (Transplant Diagnostics) Thermo Fisher Scientific Inc

Manager Regulatory Affairs Bioventus Inc

Regulatory Affairs Project Manager, US Remote Fortrea Inc

Senior Regulatory Affairs Consultant (Program / Client Partnership Manager) Parexel International Corp

Regulatory Affairs Project Manager, US Remote Fortrea

Senior Manager, Regulatory Affairs (Ad Promo) IRE

Senior Regulatory Affairs Consultant (Program / Client Partnership Manager) Parexel

Manager/Sr. Manager, Regulatory Affairs (Labeling) Grifols SA

Regulatory Affairs and Licensing Leader GE Vernova Inc

Manager, Government Affairs North Carolina's Electric Cooperatives

Strategy Lead, CMC Mature, Regulatory Affairs GSK plc

Research Scientist - Epidemiology and Scientific Affairs Thermo Fisher Scientific Inc

Director of Admissions Brody School of Medicine East Carolina University

Director of Academic Advising, Duke University School of Law Duke University

Director of Business Development, Life Sciences (HEOR) Staffing MeeDerby

Associate Director of Housing Operations & Facilities Davidson College

Director of Legal - N-A M&A Circle K Stores Inc

Deputy Director of Finance (Signing Bonus Eligible Position) City Of Greensboro

Deputy Director of Finance (Financial and Administrative Services) City Of Greensboro

Director of Government Relations Progress Residential

ViiV Healthcare (GSK) Medical Director, ViiV R&D Physician Center of Excellence GSK plc

Director of Public Safety Guilford College

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