Gilead Sciences, Inc.
Director, Clinical Development Inflammation (MD)
Gilead Sciences, Inc., Foster City, California, United States, 94420
Director, Clinical Development Inflammation (MD)
POSITION OVERVIEW:You will typically lead multiple components of clinical trial programs in IBD/inflammation clinical development. You may also act as the Physician Responsible on certain projects. For the assigned projects, you are accountable for various aspects of ongoing clinical trial program-related activities. These activities include, but are not limited to, study protocol preparation, additional study or investigator documentation, contributions to data analysis plans, study reporting, and clinical development inputs into regulatory documentation, publications, and scientific presentations.EXAMPLE RESPONSIBILITIES:Provides input into or leads the development of the Target Product Profile and Clinical Development Plan for assigned molecules/products.Provides scientific and clinical guidance to cross-functional teams and colleagues to meet clinical development project deliverables and timelines.Provides input into, or otherwise leads, clinical trial protocol design, clinical study reports, and health authority inquiries.Provides ongoing medical monitoring for clinical trials, including but not limited to assessment of eligibility criteria, toxicity management, and drug safety surveillance.Manages the clinical development component(s) in the preparation/review of regulatory documents, investigator brochures, and development plans.Coordinates the collection and assimilation of ongoing data for internal analysis and review.Coordinates and manages the preparation and/or review of data listings, summary tables, study results, and scientific presentations.Presents scientific information at scientific conferences as well as clinical study investigator meetings.Adheres to regulatory requirements of study conduct and industry standards of Good Clinical Practice as well as Gilead SOPs.REQUIREMENTS:We are all different, yet we all use our unique contributions to serve patients. Please see the following for the qualifications and skills we seek for this role.Minimum Education & ExperienceMD or equivalent with 4+ years’ clinical, scientific and/or drug development experience in the biopharma industry, healthcare, consulting, academia or a related environment.Board certification in Gastroenterology is preferred, including familiarity with IBD management or inflammatory disease management.Experience in the biopharma industry is preferred.Significant experience working on, with and leading cross-functional project/program teams in life sciences, healthcare, consulting or academia.Experience taking the lead on study concept and protocol design, regulatory filings, clinical publications, and presentations.Demonstrated excellence in complex project management and effectively managing multiple clinical project deliverables and priorities through matrix management and leadership.Knowledge & Other RequirementsProven analytical abilities as demonstrated through past experience and/or academic research.Has core expertise in the assigned or related disease area, as evidenced by the ability to independently lead clinical development for deliverables for one or more projects.Has a thorough understanding of pharmaceutical regulatory requirements and impact on development and execution of clinical trials.Has advanced knowledge of R&D and major disease areas, as evidenced by effectiveness supporting clinical projects.Strong communication and organizational skills. Demonstrable abilities to effectively communicate project direction and status to varying organizational levels, including leadership teams, executives, and steering committees.When needed, ability to travel.Open to only WEST COAST candidates or candidates who are open to relocation.The salary range for this position is: $248,115.00 - $321,090.00. 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:
Gilead BenefitsAs an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, 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.
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POSITION OVERVIEW:You will typically lead multiple components of clinical trial programs in IBD/inflammation clinical development. You may also act as the Physician Responsible on certain projects. For the assigned projects, you are accountable for various aspects of ongoing clinical trial program-related activities. These activities include, but are not limited to, study protocol preparation, additional study or investigator documentation, contributions to data analysis plans, study reporting, and clinical development inputs into regulatory documentation, publications, and scientific presentations.EXAMPLE RESPONSIBILITIES:Provides input into or leads the development of the Target Product Profile and Clinical Development Plan for assigned molecules/products.Provides scientific and clinical guidance to cross-functional teams and colleagues to meet clinical development project deliverables and timelines.Provides input into, or otherwise leads, clinical trial protocol design, clinical study reports, and health authority inquiries.Provides ongoing medical monitoring for clinical trials, including but not limited to assessment of eligibility criteria, toxicity management, and drug safety surveillance.Manages the clinical development component(s) in the preparation/review of regulatory documents, investigator brochures, and development plans.Coordinates the collection and assimilation of ongoing data for internal analysis and review.Coordinates and manages the preparation and/or review of data listings, summary tables, study results, and scientific presentations.Presents scientific information at scientific conferences as well as clinical study investigator meetings.Adheres to regulatory requirements of study conduct and industry standards of Good Clinical Practice as well as Gilead SOPs.REQUIREMENTS:We are all different, yet we all use our unique contributions to serve patients. Please see the following for the qualifications and skills we seek for this role.Minimum Education & ExperienceMD or equivalent with 4+ years’ clinical, scientific and/or drug development experience in the biopharma industry, healthcare, consulting, academia or a related environment.Board certification in Gastroenterology is preferred, including familiarity with IBD management or inflammatory disease management.Experience in the biopharma industry is preferred.Significant experience working on, with and leading cross-functional project/program teams in life sciences, healthcare, consulting or academia.Experience taking the lead on study concept and protocol design, regulatory filings, clinical publications, and presentations.Demonstrated excellence in complex project management and effectively managing multiple clinical project deliverables and priorities through matrix management and leadership.Knowledge & Other RequirementsProven analytical abilities as demonstrated through past experience and/or academic research.Has core expertise in the assigned or related disease area, as evidenced by the ability to independently lead clinical development for deliverables for one or more projects.Has a thorough understanding of pharmaceutical regulatory requirements and impact on development and execution of clinical trials.Has advanced knowledge of R&D and major disease areas, as evidenced by effectiveness supporting clinical projects.Strong communication and organizational skills. Demonstrable abilities to effectively communicate project direction and status to varying organizational levels, including leadership teams, executives, and steering committees.When needed, ability to travel.Open to only WEST COAST candidates or candidates who are open to relocation.The salary range for this position is: $248,115.00 - $321,090.00. 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:
Gilead BenefitsAs an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, 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.
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