Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted 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 Revolutionariesin a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
The Opportunity:
The Senior Director Real-World Data & Analytics will work with the Executive Director Head of Epidemiology and VP of HEOR to establish the RWD&A group at RevMed scaling organizational capabilities and leading the strategy and execution of key RWD&A deliverables for RevMed assets. They will be accountable for working across the clinical development safety medical affairs commercial including analytics and insights and IT matrix developing strategies and leading and/or overseeing execution of key projects. Reporting to the Executive Director Head of Epidemiology & RWD Strategy they will closely align with the other users of RWD at RevMed develop ways of working and communication channels to maximize RevMeds investment in RWD as well as lead the analysis (either directly or leveraging junior team members and vendors) of RWD database and other studies. This is an exceptional opportunity to contribute to the advancement of oncology by leveraging real-world data and analytics that will shape the future of patient care.
Develop and lead RWD and analytics plans to support portfolio Medical Affairs HEOR/RWE and epidemiology goals.
Provide subject matter expertise on RWD data sources their strengths/limitations and the feasibility of answering key scientific questions using available data.
Oversee high-quality RWE study design protocol development statistical analysis planning and final reporting in support of regulatory submissions and product value evidence typical projects include include systematic literature reviews natural history studies clinical trial design and optimization comparative effectiveness and safety and healthcare resource utilization types of studies post-approval safety studies leveraging RWD as well as RWD-related insights such as quick feasibility and information used to inform our fast-moving clinical programs.
Ensure fit-for-purpose methods are used to provide scientific rigor to non-interventional studies so that they adhere to global regulatory guidance frameworks and are acceptable to other key stakeholders.
Provide thought leadership in advanced analytic techniques (e.g. causal inference predictive modeling AI/ML) that reflect current industry practices.
Communicate insights and analysis effectively to senior stakeholders regulatory agencies payers and scientific audiences through written reports and presentations.
Participate in governance feasibility review and multidisciplinary project teams ensuring RWD analytics add meaningful insight at key decision points.
Build mentor and lead a high-performing analytics team with expertise in epidemiology biostatistics data science and RWE methodologies.
Drive adoption of robust analytics standards and tools that enhance consistency and scalability of RWD efforts across projects including partnership with other functions to establish data ingestion pipelines and support the establishment of data lakes.
Required Skills Experience and Education:
PhD / DSc / DrPH in epidemiology or biostatistics or a relevant advanced science degree and at least 12 years of experience with RWD analytics and evidence generation in pharma/biotech.
Demonstrated experience leading complex RWD/RWE projects from concept through delivery including study design analysis and reporting/submission to regulatory agencies.
Strong expertise with RWD sources (claims EHR registries -omics data linked datasets) and analytic tools (R/SAS/Python).
Demonstrated technical knowledge of epidemiologic biostatistical and data science methods.
Knowledgeofdrugandclinical developmentprocessforgenomic/targeted medicines.
Excellentanalyticandproblem-solving skills.
Stronginterpersonal skillsandthe abilitytowork effectivelyinmultidisciplinary teamsincluding abilitytoprovide oversighttovendors.
Preferred Skills:
Experience in oncology RWD&A.
Track record of publications or presentations in RWD&A/epidemiology/data science.
Experience aligning RWE strategy to regulatory and payer evidence planning especially around the planning and execution of post-approval safety studies.
#LI-Remote #LI-VN1
The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role level and location. Individual base pay salary is determined by multiple factors including job-related skills experience market dynamics and relevant education or training.
Please note that base pay salary range is one part of the overall total rewards program at RevMed which includes competitive cash compensation robust equity awards strong benefits and significant learning and development opportunities.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race color religion gender sexual orientation gender identity/expression national origin/ancestry age disability marital status medical condition and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect process and use any personal data that you provide to us in accordance with ourCCPA additional information please contact.
Base Pay Salary Range
$244000$305000 USD
Required Experience:
Exec
Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The companys R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins and RAS Compa...
Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted 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 Revolutionariesin a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
The Opportunity:
The Senior Director Real-World Data & Analytics will work with the Executive Director Head of Epidemiology and VP of HEOR to establish the RWD&A group at RevMed scaling organizational capabilities and leading the strategy and execution of key RWD&A deliverables for RevMed assets. They will be accountable for working across the clinical development safety medical affairs commercial including analytics and insights and IT matrix developing strategies and leading and/or overseeing execution of key projects. Reporting to the Executive Director Head of Epidemiology & RWD Strategy they will closely align with the other users of RWD at RevMed develop ways of working and communication channels to maximize RevMeds investment in RWD as well as lead the analysis (either directly or leveraging junior team members and vendors) of RWD database and other studies. This is an exceptional opportunity to contribute to the advancement of oncology by leveraging real-world data and analytics that will shape the future of patient care.
Develop and lead RWD and analytics plans to support portfolio Medical Affairs HEOR/RWE and epidemiology goals.
Provide subject matter expertise on RWD data sources their strengths/limitations and the feasibility of answering key scientific questions using available data.
Oversee high-quality RWE study design protocol development statistical analysis planning and final reporting in support of regulatory submissions and product value evidence typical projects include include systematic literature reviews natural history studies clinical trial design and optimization comparative effectiveness and safety and healthcare resource utilization types of studies post-approval safety studies leveraging RWD as well as RWD-related insights such as quick feasibility and information used to inform our fast-moving clinical programs.
Ensure fit-for-purpose methods are used to provide scientific rigor to non-interventional studies so that they adhere to global regulatory guidance frameworks and are acceptable to other key stakeholders.
Provide thought leadership in advanced analytic techniques (e.g. causal inference predictive modeling AI/ML) that reflect current industry practices.
Communicate insights and analysis effectively to senior stakeholders regulatory agencies payers and scientific audiences through written reports and presentations.
Participate in governance feasibility review and multidisciplinary project teams ensuring RWD analytics add meaningful insight at key decision points.
Build mentor and lead a high-performing analytics team with expertise in epidemiology biostatistics data science and RWE methodologies.
Drive adoption of robust analytics standards and tools that enhance consistency and scalability of RWD efforts across projects including partnership with other functions to establish data ingestion pipelines and support the establishment of data lakes.
Required Skills Experience and Education:
PhD / DSc / DrPH in epidemiology or biostatistics or a relevant advanced science degree and at least 12 years of experience with RWD analytics and evidence generation in pharma/biotech.
Demonstrated experience leading complex RWD/RWE projects from concept through delivery including study design analysis and reporting/submission to regulatory agencies.
Strong expertise with RWD sources (claims EHR registries -omics data linked datasets) and analytic tools (R/SAS/Python).
Demonstrated technical knowledge of epidemiologic biostatistical and data science methods.
Knowledgeofdrugandclinical developmentprocessforgenomic/targeted medicines.
Excellentanalyticandproblem-solving skills.
Stronginterpersonal skillsandthe abilitytowork effectivelyinmultidisciplinary teamsincluding abilitytoprovide oversighttovendors.
Preferred Skills:
Experience in oncology RWD&A.
Track record of publications or presentations in RWD&A/epidemiology/data science.
Experience aligning RWE strategy to regulatory and payer evidence planning especially around the planning and execution of post-approval safety studies.
#LI-Remote #LI-VN1
The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role level and location. Individual base pay salary is determined by multiple factors including job-related skills experience market dynamics and relevant education or training.
Please note that base pay salary range is one part of the overall total rewards program at RevMed which includes competitive cash compensation robust equity awards strong benefits and significant learning and development opportunities.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race color religion gender sexual orientation gender identity/expression national origin/ancestry age disability marital status medical condition and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect process and use any personal data that you provide to us in accordance with ourCCPA additional information please contact.
Base Pay Salary Range
$244000$305000 USD
Required Experience:
Exec
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