At Gilead were creating a healthier world for all people. For more than 35 years weve 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 worlds biggest health challenges and our mission requires collaboration determination and a relentless drive to make a difference.
Every member of Gileads 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 were 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
Provides local medical and scientific expertise to support global product development launch and lifecycle activities ensuring countryspecific considerations are incorporated into medical plans.
Represents the company in scientific exchange with healthcare professionals professional societies cooperative groups and other external stakeholders at national and international scientific meetings.
Leads execution of countrylevel medical plans with cooperative groups to identify evidence gaps and local medical needs; supports development of solutions aligned with medical strategy.
Supports the generation of local clinical evidence through participation in clinical trials investigatorinitiated studies and observational or realworld evidence activities.
Contributes to the planning and execution of local Health Economics and Outcomes Research (HEOR) activities in collaboration with crossfunctional partners.
Provides medical input to local market access strategies by delivering scientific and clinical components of access and value plans in coordination with Market Access Regulatory and Commercial teams.
Supports coordination of the local Medical Affairs function by managing assigned projects priorities timelines and interfaces with internal and external stakeholders.
Develops and executes prelaunch and postlaunch Medical Affairs plans for assigned products and indications ensuring delivery of defined medical deliverables.
Manages assigned medical budget components and monitors expenditures versus plan within agreed parameters ensuring appropriate governance and documentation.
Provides medical input into crossfunctional discussions to support alignment and execution of agreed strategic priorities.
Contributes to International Region Medical Affairs initiatives by sharing local insights and executing assigned regional projects or deliverables.
Leads or supports data generation initiatives within assigned scope coordinating activities and ensuring timely completion of objectives.
Maintains regular interaction with the external medical community to remain current on scientific developments and evolving standards of care.
Engages in peertopeer scientific exchange of complex clinical and scientific information using approved data and materials.
Develops and maintains strong scientific relationships with thought leaders disease experts and other healthcare professionals within the assigned scope.
Delivers clinical and scientific presentations to internal and external audiences in accordance with medical strategy and compliance standards.
Collects and communicates compliant insights from healthcare professional interactions to internal stakeholders to inform medical planning and execution.
Supports clinical trial site engagement activities including initiatives aimed at supporting enrollment and study conduct.
Provides Medical Affairs support at professional meetings and congresses including scientific session coverage and facilitation of interactions with healthcare professionals.
Ensures compliance with corporate policies healthcare regulations and ethical standards across all Medical Affairs activities.
Maintains uptodate clinical scientific and technical knowledge in hematology/oncology and relevant therapeutic areas.
Establishes and maintains ongoing collaborative relationships with healthcare professionals within the assigned territory or centers.
Responds to and documents unsolicited requests for medical or scientific information in accordance with internal procedures.
Provides medical input and training to internal teams as requested to support appropriate and compliant use of scientific information.
Supports planning and delivery of Advisory Boards and other scientific forums including content review and insight capture.
Collaborates with fieldbased and headquarters colleagues to support timely response to site and stakeholder questions.
Attends major scientific congresses and supports coordination of Medical Affairs activities; may present to external audiences as appropriate.
Develops and executes medical projects within assigned scope to address emerging scientific clinical or data needs.
Performs medical review activities within Promotional Review Committees in line with governance and regulatory requirements.
Manages projects to completion by coordinating stakeholders monitoring progress and addressing issues in a collaborative manner.
Advanced degree in a healthcare or lifescience discipline (e.g. MD PharmD PhD MSc) with solid clinical and/or scientific experience in oncohematology.
Demonstrated experience in Medical Affairs within the pharmaceutical or biotech industry with handson involvement in oncohematology product support and lifecycle activities.
Prior experience in a Medical Manager Senior Medical Manager or equivalent role or demonstrated accountability for medical strategy execution at country or diseasearea level.
Experience leading coordinating or linemanaging Medical Science Liaisons (MSLs) including setting priorities providing scientific guidance and supporting performance and development is strongly preferred.
Prior participation in at least one product launch or major indication expansion within oncohematology is strongly preferred.
Experience with advanced or innovative therapies (e.g. CART cell therapy cellular therapies immunooncology bispecific antibodies) is a strong advantage.
Proven ability to manage multiple medical projects simultaneously prioritize activities and deliver against timelines with a high level of autonomy.
Strong written and verbal communication skills with the ability to clearly and credibly communicate complex scientific and clinical information to internal and external stakeholders.
Demonstrated capability to engage effectively in peertopeer scientific exchange with hematologists and oncologists across academic and community settings.
Strong presentation skills including experience delivering scientific and clinical content in advisory boards medical education programs and congress settings.
Demonstrated informal or formal leadership experience including crossfunctional project leadership mentoring of junior colleagues or coordination of field medical activities.
Sound scientific judgment high integrity and the ability to operate effectively in a highly regulated compliancedriven Medical Affairs environment.
Willingness and ability to travel domestically and internationally including occasional weekend travel to support congresses advisory boards and Medical Affairs activities.
Fluent Portuguese and English required for effective local and international collaboration.
Please apply via the Internal Career Opportunities portal in Workday.
Required Experience:
Manager
Gilead Sciences is continuing to hire for all open roles. Our interview process may be conducted virtually and some roles will be asked to temporarily work from home. Over the coming weeks and months, we will be implementing a phased approach to bringing employees back to site to ensu ... View more