Associate Director, Global Medical Information
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What you'll do
- Develops, reviews and maintains Medical Information resources, including standard response documents (SRDs), custom response letters (CRLs), FAQs and other approved response materials.
- Ensures all Medical Information content is scientifically accurate, evidence-based, consistent with the latest clinical data, and compliant with applicable regulatory requirements, industry codes and medical information standards.
- Supports the management of unsolicited inquiries from healthcare professionals, patients and caregivers, ensuring responses are accurate, compliant and timely.
- Monitors and analyzes Medical Information inquiry trends and customer insights to identify emerging scientific information needs, inform content development, and recommend operational improvements.
- Provides Medical Information and scientific support related to companion diagnostics associated with therapeutic assets, ensuring aligned communication across relevant stakeholders.
- Supports Medical Information activities at scientific congresses, including preparation of congress-specific Medical Information resources and staffing Medical Information booths.
- Contributes to the development, implementation, and maintenance of Medical Information SOPs, work instructions, and operational processes to support compliance with applicable regulatory requirements, industry standards, and company policies.
- Monitors relevant scientific publications and clinical trial data to inform Medical Information content and strategy.
- Partner cross-functionally with Medical Affairs, Clinical Development, Regulatory, Legal/Compliance, Safety, Commercial, and other stakeholders to support launch readiness and product lifecycle needs.
- Provides Medical Information expertise and support for additional Medical Affairs initiatives and projects as needed.
What they're looking for
- Advanced degree in a scientific or medical discipline; doctoral degree preferred (PharmD, MD, PhD).
- Experience supporting Medical Information activities within the pharmaceutical or biotechnology industry, including familiarity with applicable regulatory and compliance requirements.
- Excellent verbal and written communication skills.
- Experience creating, reviewing and managing scientific content for diverse audience.
- Strong organizational, problem-solving and project management skills.
- Demonstrated ability to collaborate effectively with cross-functional stakeholders and external partners.
- Self-motivated, with the ability to exercise sound judgment, work with appropriate autonomy, and adapt to changing priorities.
- Proficiency in medical information databases, content management systems and other relevant software tools.
- Experience with Veeva PromoMats preferred.
- Willingness to travel, approximately 10-20%.
Nice to have
- Minimum of 8 years of experience in Medical Affairs or a related field within the biotech or pharmaceutical industry.
- Experience in oncology therapeutic area; experience supporting launch readiness preferred.
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.
Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.
The Opportunity:
We are seeking a motivated and experienced professional to join our Global Medical Information team as an Associate Director of Medical Information. This role focuses on ensuring the delivery of timely, accurate, and evidence-based responses to healthcare professionals (HCPs), patients, and caregivers.
As a key member of the Medical Affairs team, this individual will support the development and execution of Medical Information activities across the product lifecycle, including the creation and maintenance of scientific response content, support of Medical Information contact center operations and scientific congresses. The ideal candidate is a skilled communicator with strong scientific background, demonstrated Medical Information expertise, and ability to manage multiple priorities in a dynamic environment.
Key Responsibilities:
-
Develops, reviews and maintains Medical Information resources, including standard response documents (SRDs), custom response letters (CRLs), FAQs and other approved response materials.
-
Ensures all Medical Information content is scientifically accurate, evidence-based, consistent with the latest clinical data, and compliant with applicable regulatory requirements, industry codes and medical information standards.
-
Supports the management of unsolicited inquiries from healthcare professionals, patients and caregivers, ensuring responses are accurate, compliant and timely.
-
Monitors and analyzes Medical Information inquiry trends and customer insights to identify emerging scientific information needs, inform content development, and recommend operational improvements.
-
Provides Medical Information and scientific support related to companion diagnostics associated with therapeutic assets, ensuring aligned communication across relevant stakeholders.
-
Supports Medical Information activities at scientific congresses, including preparation of congress-specific Medical Information resources and staffing Medical Information booths.
-
Contributes to the development, implementation, and maintenance of Medical Information SOPs, work instructions, and operational processes to support compliance with applicable regulatory requirements, industry standards, and company policies.
-
Monitors relevant scientific publications and clinical trial data to inform Medical Information content and strategy.
-
Partner cross-functionally with Medical Affairs, Clinical Development, Regulatory, Legal/Compliance, Safety, Commercial, and other stakeholders to support launch readiness and product lifecycle needs.
-
Provides Medical Information expertise and support for additional Medical Affairs initiatives and projects as needed.
Required Skills, Experience and Education:
-
Advanced degree in a scientific or medical discipline; doctoral degree preferred (PharmD, MD, PhD).
-
Experience supporting Medical Information activities within the pharmaceutical or biotechnology industry, including familiarity with applicable regulatory and compliance requirements.
-
Excellent verbal and written communication skills.
-
Experience creating, reviewing and managing scientific content for diverse audience.
-
Strong organizational, problem-solving and project management skills.
-
Demonstrated ability to collaborate effectively with cross-functional stakeholders and external partners.
-
Self-motivated, with the ability to exercise sound judgment, work with appropriate autonomy, and adapt to changing priorities.
-
Proficiency in medical information databases, content management systems and other relevant software tools.
-
Experience with Veeva PromoMats preferred.
-
Willingness to travel, approximately 10-20%.
Preferred Skills:
-
Minimum of 8 years of experience in Medical Affairs or a related field within the biotech or pharmaceutical industry.
-
Experience in oncology therapeutic area; experience supporting launch readiness preferred.
#LI-VN1 #LI-Remote
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 our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.
We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.
Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.
If you believe you’ve been contacted by someone impersonating a Revolution Medicines recruiter, please report it to careers@revmed.com so we can share these impersonations with our IT team for tracking and awareness.
Company
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