Director, Global Medical Affairs, Lung

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RASaddicted cancers. The companys R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding Revolutionaries in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
Reporting to the Lung Cancer Medical Affairs Strategy Lead, the Director, Global Medical Affairs will be responsible for supporting the development and execution of the Global Medical Affairs (GMA) strategy and tactical plans for Revolution Medicines assets being developed for the treatment of lung cancer. The successful candidate will have a proven track record of developing and driving medical strategy with a focus on effectively communicating key scientific data through publications, medical information, medical communications, congress activities as well as gathering insights through advisory boards and Key Opinion Leader (KOL) engagements.
Develop and execute the GMA strategy and medical objectives including activities related to scientific engagement and communication, evidence generation, internal education, and patient advocacy.
Act as the medical representative on crossfunctional teams.
Serve as a therapeutic area content expert.
Participate in the Global Medical Affairs Team (GMAT) to execute medical strategies, contribute to the operations and oversight of medical activities, and work crossfunctionally to support associated prelaunch activities.
Provide medical leadership in scientific engagement activities with key external stakeholders through organizing and leading advisory boards, studies investigator interactions, congress activities, and peertopeer discussions with the goal of communicating scientific insights to internal teams to drive strategy.
Communicate clinical and scientific data to KOLs and other healthcare professionals through presentations, educational programs, and scientific discussions.
Represent various medical affairs functions in crossfunctional strategy team meetings including clinical and safety subteams, Global Brand Team, Global Product Team, Patient Advocacy, Market Access, and other crossfunctional strategic discussions.
Work closely with the Clinical and MSL teams to provide enrollment, scientific, and engagement support to ensure clinical trials meet study timelines.
Work with the Patient Advocacy and Grants teams to incorporate the patient voice and define external medical education strategies for independent grants, respectively.
Provide medical support for scientific symposia and medical congresses and collaborate across GMA functions to develop, review, and align on key scientific communication points and medical information response documents within legal and compliance guidelines.
Support the review and approval of abstracts, manuscripts, corporate communications, and other data disclosure documents as well as internal stakeholder medical education activities related to the compound data and related competitor data.
Collaborate with stakeholders across the organization, including, but not limited to, Clinical Development and Operations, Commercial Operations, Program Management, Business Development, Regulatory, Safety, and Compliance teams.
Advanced doctorate degree (PharmD, PhD, MD, DO or equivalent) in medical/scientific area is required.
~10+ years of relevant experience in the biotech or pharmaceutical industry focused on Medical Affairs, with global crossfunctional inhouse experience and onfield based teams.
~ Strong scientific background in lung cancer with a good understanding of biomarkerdriven disease and ability to effectively analyze, synthesize, and communicate complex scientific information.
~ Direct, handson experience executing the activities of various functions within medical affairs (training, medical communications, medical information, expanded access programs, evidence generation, publications).
~ Proven track record of clinical trial support including protocol development/review, site selection support, enrollment support, and data analysis.
~ Excellent interpersonal, written, and presentation skills with the ability to effectively communicate complex scientific data with a strong point of view to diverse audiences.
~ Thrives in fastpaced, dynamic environment and ability to multitask independently with limited supervision.
~ Ability to travel to Redwood City headquarters and professional congresses (3040%).
~ Strong networking skills with deep existing relationships with lung cancer healthcare professionals including global top key opinion leaders required.

Experience in global product launches including support of integrated brand plan ideation, regulatory submissions, reimbursement, and label development.
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