Medical Director

• Lead medical strategy and external engagement for the VEXAS disease area
• Serve as the lead medical voice for VEXAS
• Drive the US medical strategy and partner closely with Field Medical to engage and educate healthcare providers (HCPs), medical organizations, payers, and patient advocacy groups
• Lead planning and execution of advisory boards and educational activities
• Generate and share medical insights with internal partners
• Build strong collaborative relationships across Market Access, Medical Information, Clinical Development, Sales, and Marketing
• Contribute to evidence generation projects, real-world evidence studies, and publications supporting the VEXAS disease area
• Support launch readiness through disease education and evidence generation planning

Hematology Medical Director – VEXAS

• Leads the development of the annual medical strategic plan together with Medical Affair leadership team.
• Contributes to the medical evidence generation strategy, including real-world evidence (RWE), investigator-sponsored studies (IIS), and collaborative research efforts.
• Provides medical input into clinical development plans, target product profiles, and lifecycle management strategies across pipeline and marketed products.
• Builds and maintains trusted partnerships with key opinion leaders, academic experts, and healthcare providers.
• Serves as an internal medical advisor and point of contact for key cross-functional teams and committees.
• Contributes to publication strategy development in partnership with cross-functional colleagues.
• Supports pipeline planning and early-phase development efforts, providing medical input.

Medical Director, Infectious Diseases

• Design, execute, and scale clinical development programs for precision oncology diagnostics
• Ensure alignment with real-world clinical decision-making and guideline development
• Define diagnostic-focused study priorities and oversee study execution
• Serve as a subject matter expert and lead working groups for oncology studies
• Establish external partnerships for high-quality study execution
• Lead scientific communication and evidence dissemination
• Support regulatory strategy and compliance

Clinical Program Director – Precision Oncology Diagnostics, MRD Focus

• Guide teams in content development and medical strategy
• Provide strategic input into account planning
• Build and nurture client relationships
• Identify business development opportunities
• Lead strategy execution in collaboration with teams
• Facilitate meetings and workshops

Associate Medical Strategy Director

• Provide expert guidance and oversight for physical health service requests
• Ensure the integrity and quality of utilization management activities
• Participate in internal reviews of inpatient and outpatient clinical case types
• Apply medical necessity criteria utilizing review criteria hierarchy
• Complete expected case volume as expected by the department
• Follow department processes as defined by approved Alliance policies
• Support the Clinical Operations Department through active participation in organizational committees
• Provide clinical guidance and leadership to promote collaboration between medical, behavioral, and care management teams
• Maintain awareness of regulatory requirements, utilization management guidelines, and emerging trends
• Contribute to process improvement initiatives aimed at enhancing clinical quality, efficiency, and member outcomes
• Support cross functional teams with medical expertise
• Train and mentor peers within the Medical Management team

Medical Director – Physical Health

• Provides medical oversight of assigned clinical studies in the duty as a medical monitor
• Provides medical input and oversight in support of the Drug Safety and Pharmacovigilance department
• Develops and delivers project-specific and therapeutic training to project team members and clinical site staff
• Provides medical input into data collection tools, monitoring plans, and review and analysis plans
• Provides oversight to assigned Medical Scientist staff and Medical Director colleagues to review clinical data

Senior Medical Director – Immunology/Rheumatology

• Provides administrative oversight to the medical staff
• Analyzes medical review utilization data
• Researches new medical procedures or technology
• Acts as a resource to providers and internal staff on medical policies
• Writes and revises medical policies
• Supports operations in case review on medical and regulatory matters
• Develops claim adjudication criteria for situations requiring medical judgment
• Educates staff and medical community on medical policy and program administration
• Develops and updates medical policy in consultation with regulatory personnel, medical consultants, and professional societies
• Develops external relationships with the medical community
• Reviews physician and provider practice pattern analysis and statistical data related to medical service utilization
• Conducts research into new or controversial medical procedures and technology

Physical Medicine and Rehabilitation Medical Director

• Ensure individual subject safety and the scientific integrity of studies during the clinical development of United Therapeutics Corporation (UTC) products in accordance with ICH Good Clinical Practice (GCP), applicable regulatory guidelines and company standard operating procedures (SOPs)
• Provide medical expertise, advice, and guidance to members of the clinical development project teams as required and needed
• Provide medical support for routine medical inquiries for internal and external study teams and sites
• Provide on-call medical support for urgent medical inquiries
• Conduct medical monitoring activities for allocated clinical studies; including review and approval of study protocols with particular focus on study design, scheduled assessments, and protection of subject safety
• Review and approve all versions of the patient information leaflet and informed consent form templates
• Participate in the draft, review and ownership of study-specific medical monitoring plans (MMP)
• Review study statistical analysis plans
• Provide appropriate clinical training for internal and external study team members and site personnel as and when required before and during conduct of studies
• Review serious adverse events (SAEs) that occur during studies when they are notified to Global Drug Safety to assist in identifying any emergent safety concerns that may be related to study conduct
• Review safety information, including adverse events and clinical laboratory data during study conduct
• Support the Data Monitoring Committee (DMC)/Data Safety Monitoring Board (DSMB) when such a Committee is constituted for a study
• Review draft data listings, including coded data, provided by Data Management, to ensure medical consistency of the data
• Participate in the review and interpretation of study data
• Document all medical monitoring activities and communications related to allocated studies

Senior Medical Director – Medical Monitoring

• Shape clinical pharmacology strategy across drug development programs
• Apply PK/PD, pharmacometrics, and model-informed drug development approaches
• Collaborate across clinical, regulatory, biostatistics, translational, and CMC teams
• Lead high-impact work and contribute to programs that shape the future of HIV treatment and prevention

Director, Clinical Pharmacology

• Responsible for providing direction, guidance, and support to a team of MSLs in an assigned region
• Responsible for direct territory responsibilities in situations when no MSL coverage available
• Assessment, recognition, and improvement of MSL performance at the individual and group level
• Ensure the successful execution of MSL strategic, operational, and tactical plans
• Keep the executive director of MSLs informed about key information in a timely manner
• Represent Exelixis Medical Affairs as managers in the field
• Represent Medical Affairs management as a cross-functional partner within the company
• Serve as a positive role model and actively support the professional development of reports
• Lead high visibility Medical Affairs projects and be accountable for the outcomes
• Foster teamwork and continuity across the entire MSL organization
• Engage key national and regional thought leaders and healthcare professionals
• Exchange scientific information with external parties
• Report field intelligence to Exelixis including competitive information, perspectives about compounds, and the treatment landscape
• Represent Exelixis management at medical conferences and provide session summaries
• Provide cross-functional support across the company by being a scientific resource

Associate Director, Medical Science Liaison

• Serve as a senior clinical leader and addiction medicine subject matter expert across the organization.
• Partner with Clinical Services leadership to strengthen clinical quality, consistency, and patient safety across Boulder’s care delivery model.
• Lead routine review and refinement of clinical protocols, formulary standards, and evidence-based practice guidelines.
• Support quality assurance activities, chart review processes, and clinical audits to identify opportunities for improvement.
• Provide consultation and guidance on complex clinical cases and emerging clinical issues.
• Ensure Boulder’s clinical standards remain aligned with current evidence, regulatory requirements, and payer expectations.
• Partner with Clinical Services leadership to strengthen clinical leadership capabilities across the organization.
• Provide mentorship, coaching, and support to clinical leaders and clinicians navigating complex clinical and operational challenges.
• Help establish and reinforce standards of clinical excellence, professional growth, and evidence-based practice.
• Contribute physician leadership and oversight to clinician education, onboarding standards, and ongoing clinical development programs.
• Support the development of systems that promote accountability, consistency, and continuous improvement across the clinical organization.
• Translate quality findings, operational priorities, and emerging evidence into scalable clinical workflows and care delivery standards.
• Identify gaps in clinical processes, policies, and infrastructure and partner across teams to implement solutions.
• Support implementation of new clinical initiatives and ensure clinical best practices are operationally viable and consistently applied.
• Drive adoption of new clinical workflows, protocols, and care models across a distributed clinical workforce.
• Partner with Medical Affairs and Clinical Services leadership to evaluate and support expansion into new service lines and care models.
• Assess clinical readiness, staffing considerations, protocol requirements, and quality implications for new programs.
• Ensure new services are designed with appropriate clinical governance, quality standards, and outcome measurement strategies.
• Contribute clinical expertise to Boulder’s long-term vision of comprehensive substance use disorder care.
• Serve as a clinical liaison to Product, Operations, Analytics, and other cross-functional teams.
• Translate clinical priorities into product requirements, workflows, and operational processes.
• Provide clinical input on care delivery technology, clinical decision support tools, AI-enabled workflows, and platform enhancements.
• Ensure operational and product changes are evaluated through the lens of patient safety, clinician experience, clinical effectiveness, and quality.

Medical Director – Addiction Medicine, Telehealth

• Oversee the performance and growth of Customer Service, Prescription Processing, Client-specific teams, managing both internal staff and external vendors
• Lead operational excellence across central fill pharmacy networks and courier delivery operations
• Lead your team with Key Performance Indicators (KPIs) to drive business success and increase efficiency while lowering the cost-to-fill on an annual basis
• Manage quality, turnaround time (TAT), and customer satisfaction metrics to ensure FuzeRx remains the preferred infrastructure partner for telehealth and pharma partners
• Establish requirements for capabilities and reporting, collaborating cross-functionally to deliver data-driven insights
• Analyze data to forecast staffing needs based on program performance, optimizing resource allocation across multiple roles
• Lead a large team of managers, supervisors and team members, establishing an environment of positive employee engagement and experience

Director, Rx Clinical Operations

• Serve in a lead banker coverage capacity for major not-for-profit healthcare issuers nationwide
• Coordinate coverage efforts and effectively partner with regionally focused teams within Public Finance and Relationship Managers in Commercial Banking
• Develop new business opportunities, manage client relationships, and create customized solutions for complex situations
• Originate and execute finance transactions as the managing underwriter in the municipal securities sector, which can include derivatives or advisory assignments
• Develop and maintain significant depth and tenure of relationships with not-for-profit healthcare issuers
• Be recognized as an acknowledged expert in their field and be able to build upon a network of influence among municipal market professionals including chief financial officers, bond lawyers, credit providers, financial advisors, rating agencies, and key industry vendors (such as public accounting firms)
• Demonstrate the ability to work effectively with teammates, within the framework of the strategic alliance, to accomplish annual and long-term business objectives
• Represent MPG within the company, and externally in support of specific municipal finance business

Executive Director, Healthcare Public Finance

• Lead the Study Management Team and provide regular updates on trial deliverables.
• Ensure real-time tracking and documentation of trial progress.
• Maintain inspection-readiness throughout the trial lifecycle.
• Act as the primary contact for country and regional staff and internal teams.
• Partner with Global Trial Leads to oversee central trial activities from start-up to close-out.
• Create and maintain trial-specific documents (e.g., Monitoring Guidelines, ICFs, Blinding Plans).
• Establish country budgets and monitor actuals vs. forecast.

Associate Clinical Project Management Director, Cross TA

• Provides medical oversight of assigned clinical studies in the duty as a medical monitor
• Often serves as primary medical contact for customers for assigned clinical studies
• Provides medical input and oversight in support of the Drug Safety and Pharmacovigilance department
• Responsible for protocol design and development, upon request
• Provides input into protocol amendments
• Develops and delivers project-specific and therapeutic training to project team members and clinical site staff; provides training to customer staff as needed
• Provides oversight to assigned Medical Scientist staff and Medical Director colleagues to review clinical data
• Presents identified trends and issues, and mitigation strategies, to customers and project team members to minimize risks to subject safety or integrity of study data
• Represents the Company at scientific and industry meetings
• Mentors staff to ensure an appropriate level of understanding regarding sound treatment and research principles of specific therapeutic area

Senior Director – Medical Monitor, Immunology/Rheumatology

• Define and govern GCM enterprise architecture standards across Commercial & Medical IT, ensuring alignment with enterprise architecture principles, security, compliance, and business strategy.
• Serve as the primary architecture leader for strategic GCM initiatives, shaping early solution designs and guiding key architectural decisions to ensure alignment with the target-state architecture.
• Lead GCM integration and data architecture strategy, defining how systems connect through scalable, secure patterns such as APIs, event-driven architecture, data-sharing models, and enterprise data flows.
• Develop multi-year enterprise architecture and business capability roadmaps that guide the evolution of Commercial & Medical platforms in line with business priorities, value streams, and capability needs.
• Identify opportunities to simplify and rationalize the application portfolio, including reducing overlapping systems, improving integration quality, lowering total cost of ownership, and avoiding unnecessary technology fragmentation.
• Provide thought leadership on emerging technologies, including cloud services, automation, data products, AI/ML, and generative AI, evaluating their fit for GCM business needs and integrating high-value capabilities with the appropriate security and compliance controls.
• Partner with cross-functional IT teams, including enterprise integration, data and analytics, security, infrastructure, delivery, and platform teams, to ensure architecture decisions are practical, scalable, and executable.
• Mentor and guide solution architects, platform architects, technical leads, and delivery teams to drive consistency in solution design and adoption of architecture best practices.
• Represent GCM in enterprise architecture forums, ensuring Commercial & Medical priorities are considered in cross-functional technology decisions.

Associate Director, Enterprise Architecture, Global Commercial & Medical IT

• Provides administrative oversight to the medical staff
• Analyzes medical review utilization data
• Researches new medical procedures or technology
• Acts as a resource to providers and internal staff on issues concerning medical policies
• Supports operations in the form of case review on both medical and regulatory matters
• Develops claim adjudication criteria for situations requiring medical judgment
• Provides input on issues and operational policies, processes, and procedures
• Educates staff and medical community on various aspects of medical policy and program administration
• Develops and updates medical policy in consultation with regulatory personnel, medical consultants, and professional societies
• Develops external relationships with the medical community and serves as liaison between these entities and the contractors
• Reviews physician and provider practice pattern analysis and other statistical data related to unusual medical service utilization
• Conducts research into new or controversial medical procedures and technology

• Prepare clinical development plans according to the nature of the clinical project and its objectives
• Oversee protocol development from concept to final protocol
• Serve as sponsor contact for key study sites on protocol related topics
• Write, edit, and review medical and scientific elements of both internal and external facing documents inclusive of clinical research
• Manage Key Opinion Leader and Medical Advisory Board interactions
• Assist Clinical Operations with supervision of activities of contract research organizations by reviewing key study plans and performance/quality

Senior Director, Clinical Development

• Manages a project as Project Manager overseeing interdisciplinary clinical research programs ensuring compliance with Good Clinical Practices (GCPs), relevant Standard Operating Procedures (SOPs) and regulatory requirements.
• Acts as primary liaison between the Company and the Customer to ensure project launch, conduct, and closeout according to the Customer’s and the Company's contractual agreement.
• Leads clinical team to ensure quality, timelines and budget management.
• Accountable for the financial performance of assigned projects.
• Accountable for all project deliverables for assigned projects and/or project regions.
• Coordinates activities and deliverables of all project conduct partners and proactively identifies and manages issues.
• Maintains and evaluates project progress by maintaining timelines and other tracking/analysis tools.
• Responsible for project management components of inspection readiness for all aspects of the project conduct, including Trial Master Files.
• Provides oversight for development and implementation of project plans in accordance with Controlled Documents.
• Independently prepares, coordinates, and presents project material at internal and external meetings.
• Directs the activities of assigned Project Support staff; line manages and mentors other project management team members and clinical staff; facilitates team building and communication.
• Prepares project management reports for clients and management.

Clinical Senior Project Manager, Associate Director – Global role, Multisponsor

• Provides administrative oversight to medical staff
• Analyzes medical review utilization data
• Researches new medical procedures or technology
• Acts as a resource to providers and internal staff on medical policy issues
• Writes and revises medical policies
• Supports operations in case review on medical and regulatory matters
• Develops claim adjudication criteria for situations requiring medical judgment
• Provides input on issues and operational policies, processes, and procedures
• Educates staff and medical community on medical policy and program administration
• Develops and updates medical policies in consultation with regulatory personnel and consultants
• Develops external relationships with the medical community
• Reviews physician and provider practice pattern analysis and other statistical data
• Conducts research into new or controversial medical procedures and technology

Medical Director jobs in North Carolina

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Hematology Medical Director – VEXAS

Medical Director, Infectious Diseases

Clinical Program Director – Precision Oncology Diagnostics, MRD Focus

Associate Medical Strategy Director

Medical Director – Physical Health

Senior Medical Director – Immunology/Rheumatology

Physical Medicine and Rehabilitation Medical Director

Senior Medical Director – Medical Monitoring

Director, Clinical Pharmacology

Associate Director, Medical Science Liaison

Medical Director – Addiction Medicine, Telehealth

Director, Rx Clinical Operations

Executive Director, Healthcare Public Finance

Associate Clinical Project Management Director, Cross TA

Senior Director – Medical Monitor, Immunology/Rheumatology

Associate Director, Enterprise Architecture, Global Commercial & Medical IT

Physical Medicine and Rehabilitation Medical Director

Senior Director, Clinical Development

Clinical Senior Project Manager, Associate Director – Global role, Multisponsor

Physical Medicine and Rehabilitation Medical Director