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Sr Director, Medical Affairs
Sr Director, Medical AffairsGilead Sciences, Inc. • Foster City, CA, United States
Sr Director, Medical Affairs

Sr Director, Medical Affairs

Gilead Sciences, Inc. • Foster City, CA, United States
30+ days ago
Job type
  • Full-time
  • Part-time
Job description

Sr Director, Medical Affairs

United States - California - Foster City Medical Affairs Regular

Job Description

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Job Description

This position is a member of the Medical Affairs Research (MAR) Leadership Team and will report to the VP, Head of MAR.

Key Responsibilities :

  • Ensures operational oversight of Investigator Sponsored Research (ISR) and Collaborative studies including but not limited to Fair Market Value and feasibility assessment, contract negotiation support, tracking and publication follow-up
  • Ensures operational oversight of Managed Access Programs (MAP), including but not limited to Compassionate Use Program (CUP) and Expanded Access Program (EAP)
  • Develops and implements a strategic plan to drive continuous improvements in the operational aspects of the studies under the purview of the team, including interactions with CROs
  • Primary liaison to the Development Clinical Operations group to make sure processes, policies and talent management approaches are optimally aligned
  • Leads and manages a team of direct reports and may manage other people leaders. Hires, develops and retains diverse top talent in the team. Sets goals for the team and individual direct reports. Coaches direct reports on their performance, development and career interests
  • Collaboration with colleagues in Clinical Operations, Medical Affairs, Real World Evidence, Health Economics and Outcomes Research, Project Management, Regulatory, Biometrics, Clinical Research and Affiliates globally ensuring delivery of assigned studies
  • Leads development of all resource plans for all assigned programs across multiple therapy areas to ensure optimal deployment and allocation of internal and external resources (ARO / CRO / FSP)
  • Makes significant contributions to our abilities to hire, develop and retain diverse talent with impact in and outside own team
  • Ability to initiate and lead departmental or interdepartmental strategic initiatives
  • Proven ability to effectively communicate scientific, medical, and organizational concepts to internal and external customers
  • Contributes leadership input into all study-related documentation, including study protocols
  • May lead development of standard operating procedures (SOPs) and other procedures or documentation within Medical Affairs and / or cross-functionally
  • Initiates continuous efforts in reviewing and identifying best practices among study teams and enforcing standardization among teams
  • Plays a lead role in representing Medical Affairs Clinical Operations within cross-functional organizational initiatives to drive ongoing efficiencies and operational excellence

Basic Qualifications :

  • 14+ Years with BS / BA
  • OR

  • 12+ Years with MS / MA or MBA
  • Preferred Qualifications :

  • Expert knowledge of the biopharma industry, including in-depth understanding of other business functions, as evidenced by proven track record of leading organizations and teams to achieve short- and long-range strategies, plans and objectives
  • Thorough knowledge of Food & Drug Administration (FDA) and European Medicines Agency (EMA), and other applicable national regulations, International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines, Good Clinical Practice (GCP) and key Clinical Operations principles, concepts, practices, standards, processes and tools
  • Thorough understanding of global pharmaceutical regulatory requirements and impact on development and execution of clinical trials
  • Strong financial acumen necessary for the management of clinical trial budgets
  • Exceptional interpersonal skills and understanding of team dynamics
  • Strong communication and organizational skills. Demonstrable abilities to effectively communicate project direction and status to varying organizational levels, including leadership teams and executives. Able to distill complex matters into a clear business case and roadmap for execution
  • Strong negotiation and conflict resolution skills
  • Strong coaching capabilities to mentor / develop staff
  • Demonstrated effectiveness in proactively managing change
  • When needed, ability to travel
  • Core Values : Embody Gilead’s core values—integrity, inclusion, teamwork, excellence and accountability
  • Professional degree, preferably in the health sciences (BS, MS, PharmD, MD) with 10 or more years’ relevant clinical or related experience in life sciences.
  • Multiple years’ experience leading high-complexity cross-functional initiatives in life sciences, including short- and long-range strategic planning, governance, team management and oversight
  • Experience in selection and management of CROs or other vendors
  • Typically has extensive line management experience, which may include managing other people leaders, and a strong track record over successive years in hiring, managing and developing diverse top talent
  • People leader accountabilities

  • Create inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.
  • Develop talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose.
  • Empower teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.
  • The salary range for this position is : $281,010.00 - $363,660.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans

    Job Description

    At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

    Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.

    We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

    Job Description

    This position is a member of the Medical Affairs Research (MAR) Leadership Team and will report to the VP, Head of MAR.

    Key Responsibilities :

  • Ensures operational oversight of Investigator Sponsored Research (ISR) and Collaborative studies including but not limited to Fair Market Value and feasibility assessment, contract negotiation support, tracking and publication follow-up
  • Ensures operational oversight of Managed Access Programs (MAP), including but not limited to Compassionate Use Program (CUP) and Expanded Access Program (EAP)
  • Develops and implements a strategic plan to drive continuous improvements in the operational aspects of the studies under the purview of the team, including interactions with CROs
  • Primary liaison to the Development Clinical Operations group to make sure processes, policies and talent management approaches are optimally aligned
  • Leads and manages a team of direct reports and may manage other people leaders. Hires, develops and retains diverse top talent in the team. Sets goals for the team and individual direct reports. Coaches direct reports on their performance, development and career interests
  • Collaboration with colleagues in Clinical Operations, Medical Affairs, Real World Evidence, Health Economics and Outcomes Research, Project Management, Regulatory, Biometrics, Clinical Research and Affiliates globally ensuring delivery of assigned studies
  • Leads development of all resource plans for all assigned programs across multiple therapy areas to ensure optimal deployment and allocation of internal and external resources (ARO / CRO / FSP)
  • Makes significant contributions to our abilities to hire, develop and retain diverse talent with impact in and outside own team
  • Ability to initiate and lead departmental or interdepartmental strategic initiatives
  • Proven ability to effectively communicate scientific, medical, and organizational concepts to internal and external customers
  • Contributes leadership input into all study-related documentation, including study protocols
  • May lead development of standard operating procedures (SOPs) and other procedures or documentation within Medical Affairs and / or cross-functionally
  • Initiates continuous efforts in reviewing and identifying best practices among study teams and enforcing standardization among teams
  • Plays a lead role in representing Medical Affairs Clinical Operations within cross-functional organizational initiatives to drive ongoing efficiencies and operational excellence
  • Basic Qualifications :

  • 14+ Years with BS / BA
  • OR

  • 12+ Years with MS / MA or MBA
  • Preferred Qualifications :

  • Expert knowledge of the biopharma industry, including in-depth understanding of other business functions, as evidenced by proven track record of leading organizations and teams to achieve short- and long-range strategies, plans and objectives
  • Thorough knowledge of Food & Drug Administration (FDA) and European Medicines Agency (EMA), and other applicable national regulations, International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines, Good Clinical Practice (GCP) and key Clinical Operations principles, concepts, practices, standards, processes and tools
  • Thorough understanding of global pharmaceutical regulatory requirements and impact on development and execution of clinical trials
  • Strong financial acumen necessary for the management of clinical trial budgets
  • Exceptional interpersonal skills and understanding of team dynamics
  • Strong communication and organizational skills. Demonstrable abilities to effectively communicate project direction and status to varying organizational levels, including leadership teams and executives. Able to distill complex matters into a clear business case and roadmap for execution
  • Strong negotiation and conflict resolution skills
  • Strong coaching capabilities to mentor / develop staff
  • Demonstrated effectiveness in proactively managing change
  • When needed, ability to travel
  • Core Values : Embody Gilead’s core values—integrity, inclusion, teamwork, excellence and accountability
  • Professional degree, preferably in the health sciences (BS, MS, PharmD, MD) with 10 or more years’ relevant clinical or related experience in life sciences.
  • Multiple years’ experience leading high-complexity cross-functional initiatives in life sciences, including short- and long-range strategic planning, governance, team management and oversight
  • Experience in selection and management of CROs or other vendors
  • Typically has extensive line management experience, which may include managing other people leaders, and a strong track record over successive years in hiring, managing and developing diverse top talent
  • People leader accountabilities

  • Create inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.
  • Develop talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose.
  • Empower teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.
  • The salary range for this position is : $281,010.00 - $363,660.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans

    For additional benefits information, visit :

    https : / / www.gilead.com / careers / compensation-benefits-and-wellbeing

  • Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
  • For jobs in the United States :

    Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex , age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance.

    For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.

    NOTICE : EMPLOYEE POLYGRAPH PROTECTION ACT

    YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

    PAY TRANSPARENCY NONDISCRIMINATION PROVISION

    Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

    Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.

    For Current Gilead Employees and Contractors :

    Please apply via the Internal Career Opportunities portal in Workday.

    Share :

    Job Requisition ID R0046073

    Full Time / Part Time Full-Time

    Job Level Director

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    Medical Director • Foster City, CA, United States

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