Associate Director, Medical Training, Medical Information

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $186k - $225k / year

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

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Verastem Oncology

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2010

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Verastem Oncology is a clinical-stage biopharmaceutical company focused on developing novel small-molecule therapies that target the RAS/MAPK signaling pathway to treat aggressive and recurrent cancers. The company develops and advances combination therapies, including RAF/MEK clamp and FAK inhibitors (e. g. , avutometinib and defactinib), and has an FDA-approved combination for KRAS-mutant recurrent low-grade serous ovarian cancer. Verastem runs multiple clinical trials, collaborates strategically, and centers its pipeline on inhibiting RAS-driven tumor biology to improve patient outcomes.

📋 Description

• Support the development and implementation of learning and development strategies for Medical Affairs, with a focus on the Field Medical organization • Train Field Medical colleagues on Medical Information processes, disease state and product information, scientific content, and appropriate use of approved medical materials • Develop and deliver onboarding and ongoing training for MSLs and other Medical Affairs colleagues • Identify content and training needs based on scientific data, field insights, medical information inquiries, and changes to product information • Develop and maintain scientifically accurate, balanced, referenced, and compliant Field Medical training materials and core content • Support preparation for product launches, new data readouts, major congresses, publications, and significant scientific milestones • Manage external training vendors, speakers, and subject-matter experts • Own and manage Medical Information operations for marketed products • Respond to unsolicited medical information requests in a timely, accurate, balanced, and scientifically rigorous manner • Translate complex clinical and scientific data into clear, compliant medical information materials • Develop, review, and maintain standardized medical information responses and resources • Establish processes, workflows, systems support, and service standards for medical information inquiries • Manage vendors for Medical Information services, content development, or technology platforms • Monitor inquiry trends and identify emerging questions, knowledge gaps, and resource opportunities • Establish metrics and dashboards and report Medical Information insights and trends to Medical Affairs leadership • Partner with Pharmacovigilance/Safety on adverse event identification, documentation, and escalation • Maintain approved medical information resources and scientific references • Support medical information activities at scientific and medical congresses • Ensure consistent communication of approved medical and scientific information across the organization • Maintain inspection readiness and documentation of Medical Information activities • Participate in cross-functional product and launch-readiness planning as the Medical Information subject matter expert

🎯 Requirements

• Bachelor's degree in a scientific or healthcare-related discipline required • 6–8+ years of relevant experience in Medical Training, Medical Communications, Field Medical, or a related pharmaceutical/biotechnology function • Experience supporting a commercial-stage pharmaceutical or biotechnology product strongly preferred • Experience developing and maintaining medical/scientific content for Field Medical or Medical Affairs teams • Demonstrated experience managing medical information inquiries and developing scientifically rigorous medical information responses • Strong understanding of pharmaceutical product information, approved labeling, and the distinction between promotional and non-promotional medical communications • Experience working cross-functionally with Medical Affairs, Regulatory, Pharmacovigilance, Clinical Development, Commercial, Legal, and Compliance teams • Strong scientific and clinical writing skills with the ability to synthesize complex information into clear, concise, audience-appropriate content • Strong project management and organizational skills, with the ability to manage multiple priorities and deadlines in a fast-paced environment • Excellent attention to detail and commitment to scientific accuracy and compliance • Ability to work independently and effectively in a highly collaborative, cross-functional environment • Advanced scientific, medical, pharmacy, nursing, or related degree preferred • Experience supporting an oncology product or oncology Medical Affairs organization preferred • Experience supporting product launch or pre-launch Medical Affairs activities preferred • Experience developing and delivering Medical Training strategies and working directly with MSL/Field Medical teams preferred • Experience with Medical Information databases, inquiry management platforms, or content management systems preferred • Experience managing external Medical Information vendors or service providers preferred