Job Summary The Vice President (VP) of Research and Innovation is a senior leader responsible for driving Novant Health’s strategic research initiatives, overseeing clinical trials, and ensuring compliance across hospitals, clinics, and partnerships. This role provides strategic and operational leadership for all aspects of clinical research, including budgeting, performance management, and regulatory oversight, while fostering partnerships with pharmaceutical companies, academic institutions, and research consortia. The VP will collaborate with executives and interdisciplinary teams—including medical, pharmacy, IT, legal, and compliance—to enhance research engagement, advance key priorities such as mergers and acquisitions, and position Novant Health as a thought leader in the industry. With a strong focus on ethics, safety, and quality, the VP will establish governance structures, implement process improvements, and ensure adherence to federal research regulations, including IRB and human subjects’ protections. The role requires expertise in clinical trial management systems, financial analysis, and strategic planning to expand research opportunities, optimize operations, and drive innovation. Additionally, the VP will serve as a key liaison for corporate compliance, philanthropy, and external boards, strengthening Novant Health’s research reputation while ensuring fiscal and operational efficiency. Come join a remarkable team where quality care meets quality service, in every dimension, every time. #JoinTeamAubergine #NovantHealth. Let Novant Health be the destination for your professional growth. At Novant Health, one of our core values is diversity and inclusion. By engaging the strengths and talents of each team member, we ensure a strong organization capable of providing remarkable healthcare to our patients, families and communities. Therefore, we invite applicants from all group dynamics to apply to our exciting career opportunities. Responsibilities It is the responsibility of every Novant Health team member to deliver the most remarkable patient experience in every dimension, every time. + Our team members are part of an environment that fosters team work, team member engagement and community involvement. + The successful team member has a commitment to leveraging diversity and inclusion in support of quality care. + All Novant Health team members are responsible for fostering a safe patient environment driven by the principles of "First Do No Harm". Qualifications + Education: 4 Year / Bachelors Degree, required. In a relevant scientific, clinical, or business-related field. Medical Doctor, preferred. Equivalent combination of education and experience in science, clinical practice, or business may be considered, preferred. + Experience: + 10+ years leadership experience in healthcare and clinical research (pharmaceutical/med device company), including multi-stie trial management and partnerships with pharmaceutical and device research sponsors, required. + 10+ years proven track record in leadership role, preferably in pharmaceutical, biotechnology, or clinical research organization, strategy development, program implementation within large health systems, academic medical centers, or multi-site research enterprises, required. + Licensure/Certification: Research Certification, ACRP, SOCRA, RAPS or similar, required. Current CITI HSP (Human Subjects Protections) and CITI GCP (Good Clinical Practice), required. + Additional Skills (required): + Advanced degree (MD/DO, Ph.D., MBA, JD, MPH, etc.) with 15+ years of progressive leadership experience in clinical research operations, finance, or human subject research (equivalent combination of education and experience in science, clinical practice, or business may be considered). + Expertise in clinical trial management, regulatory compliance, and driving innovation in research methodologies. + Strong leadership, strategic thinking, and problem-solving skills with a proven ability to engage senior leaders and stakeholders. + High proficiency in clinical research technologies, data analysis, budget management, and resource allocation in dynamic environments. + Expertise in regulatory compliance (ICH/FDA/OHRP), clinical trial budgeting/contracting, IRB/IBC relations, and data privacy/security (HIPAA). + Strong proficiency in MS Excel, PowerPoint, Word, CTMS, and e-IRB, with experience across diverse therapeutic areas, including oncology, neurology, cardiology, and infectious disease. Job Opening ID 108651