Revolution Medicines

healthcare

Director,MedicalInformation,Japan

Japan Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Director, Medical Information, Japan at Revolution Medicines. Skills: Medical Information, Medical Affairs, scientific content creation, regulatory compliance, vendor management. ensuring the delivery of timely, accurate, and evidence-based responses to healthcare professionals (HCPs), patients, and caregivers. oversee the creation and management of medical information content”

Industry & Context.

healthcare
Problems you'll solve

problem-solving skills; analytical skills with the ability to monitor and analyze data to inform decision-making

Eligibility Requirements

Willingness to travel, approximately 10-20%

What They're Looking For.

Must Have

Minimum of 10 years of experience in Medical Affairs or a related field within the biotech or pharmaceutical industry, Advanced degree in scientific or medical (PharmD, MD, PhD), Proven experience in medical information, preferably within the pharmaceutical or biotechnology industry, Excellent verbal and written communication skills, Experience creating, reviewing and managing scientific content for diverse audiences, organizational, problem-solving and project management skills, analytical skills with the ability to monitor and analyze data to inform decision-making, Knowledge of regulatory guidelines related to medical information and safety reporting, Proficiency in medical information databases, content management systems and other relevant software tools, Experience with Veeva PromoMats, Ability to effectively negotiate and collaborate with internal stakeholders and external partners, Ability to prioritize and manage multiple projects simultaneously in a fast-paced dynamic environment, Self-motivated with ability to make sound decisions and adapt to changing priorities, Experience in managing medical information vendors

Nice to Have

preferably in oncology therapeutic area is strongly preferred

What You'll Do.

ensuring the delivery of timely

and evidence-based responses to healthcare professionals (HCPs)

oversee the creation and management of medical information content

provide scientific and operational oversight of Japan medical information call center team

contribute to medical booth asset creation

contribute to dossier development and review

provide Medical Information support at scientific congresses

collaborate cross-functionally to support both pipeline assets and companion diagnostics

reviews and maintains medical information resources such as standard response letters (SRLs)

custom response letters (CRLs)

FAQs and inquiry response guidance documents

Ensures all medical information content is evidence-based

and aligned with the latest scientific and clinical data

Supports the management of unsolicited inquiries from healthcare professionals

Serves as Medical Reviewer in the Medical

Legal and Regulatory (MLR) process

Leads or contributes to the development

review and maintenance of dossiers

Provides medical information and scientific support related to companion diagnostics

Supports the compendia submission process

Provides Medical Information support for congresses

Leads the development and maintenance of internal SOPs and processes

Train and support Medical Information call center vendor

Prepares and presents regular reports on medical information performance metrics and outcomes

Monitors relevant scientific publications and clinical trial data

How You'll Work.

Team & Collaboration

Collaborates with Clinical Operations, Clinical Development, Biology and other internal stakeholders; Collaborates with cross-functional partners; collaborate cross-functionally to support both pipeline assets and companion diagnostics; Ability to effectively negotiate and collaborate with internal stakeholders and external partners

Communication Scope

Excellent verbal and written communication skills

Process & Methodology

project management skills, Ability to prioritize and manage multiple projects simultaneously

Full Job Description

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: We are seeking a motivated and experienced professional to join our team as a Director of Medical Information supporting Japan. 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, you will oversee the creation and management of medical information content, provide scientific and operational oversight of Japan medical information call center team, contribute to medical booth asset creation, and contribute to dossier development and review. This role will also provide Medical Information support at scientific congresses and collaborate cross-functionally to support both pipeline assets and companion diagonstics. The ideal candidate is a skilled communicator with a strong scientific background and can manage projects in a dynamic environment. This role will report to the Head of Medical Information within the Global Medical Excellence team. Key Responsibilities: Develops, reviews and maintains medical information resources such as standard response letters (SRLs), custom response letters (CRLs), FAQs and inquiry response guidance documents to support accurate and timely responses to customers. Collaborates with Clinical Operations, Clinical Development, Biology and other internal stakeholders to gather insights for medical information content creation. Ensur

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