Revolution Medicines

Associate Director, Global Medical Information

Revolution Medicines$177K — $221K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • 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.
  • Excellent verbal and written communication skills.
  • Experience creating and managing scientific content for diverse audiences.
  • Strong organizational and project management skills.
  • Demonstrated ability to collaborate effectively with cross-functional stakeholders.
  • Proficiency in medical information databases, content management systems, and other relevant software tools.

Responsibilities

  • Develop and maintain Medical Information resources, including standard and custom response documents.
  • Ensure content is scientifically accurate, compliant, and based on the latest clinical data.
  • Manage unsolicited inquiries from healthcare professionals, patients, and caregivers, ensuring timely and accurate responses.
  • Monitor inquiry trends and customer insights to enhance content development.
  • Provide support related to companion diagnostics associated with therapeutic assets.
  • Prepare Medical Information resources for scientific congresses and staff booths as required.
  • Collaborate cross-functionally to support launch readiness and product lifecycle needs.

Benefits

  • Competitive cash compensation and robust equity awards.
  • Strong benefits package and significant learning and development opportunities.
  • Flexibility for remote work in a supportive team environment.
Full Job Description
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.

Base Pay Salary Range

$177,000-$221,000 USD

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 [email protected] so we can share these impersonations with our IT team for tracking and awareness.

About Revolution Medicines

Revolution Medicines is a clinical-stage precision oncology company focused on developing targeted therapies to inhibit elusive frontier targets within notorious growth and survival pathways, with particular emphasis on RAS and mTOR signaling pathways. The company's proprietary platform enables the discovery and development of small molecules that bind covalently to proteins. Revolution Medicines was founded in 2014 and is headquartered in South San Francisco, California.
Learn more about Revolution Medicines
Size
201 employees
Market Cap
$2.1 billion
Industry
Net Income
-$108.1 million
Revenue
$42.9 million
NASDAQ

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