Field Medical Director (MSL) - WEST
| Company/Institution: |
Syndax Pharmaceuticals |
| Location: |
Waltham, MA, US, MA, USA |
| Degree Requirements: |
MD, PhD, PhD and/or MD |
Salary: |
Not available |
| Job Type: |
Other |
Posted: |
November 14, 2024 |
| Job Setting: |
Corporate (Biotech or Pharmaceutical) |
Application Period: |
November 14-December 14, 2024 |
The Role:
Syndax is searching for a Medical Science Liaison (MSL) - WEST responsible for identifying, developing, and managing relationships with current and future hematology/oncology Key Opinion Leaders (KOLs) and other health care providers in academic and community practices. The MSL will be a key member of the Field Medical Affairs team at Syndax. This position will be the primary communicator of Syndax science and will be responsible for executing the national medical affairs plan within a specified territory.
Key Responsibilities:
KOL & Relationship Building
- Develop and foster strong scientific relationships with Key Opinion Leaders (KOLs), disease experts, and other health care providers (HCPs)
- Engage in peer-to-peer scientific exchange of complex clinical and scientific data and information
- Act as a primary point of contact to address scientific inquiries and deliver presentations on disease state, mechanisms of action, and clinical data, and serve as the scientific expert in support of Syndax therapeutic areas of interest
- Identify and evaluate Key Opinion Leaders (KOLs) and profile key institutions aligned with the medical strategy
- Create and maintain a strategic territory plan in developing and maintaining KOL relationships for Syndax.
Insight Generation and Dissemination
- Gather, analyze, and communicate actionable insights from the field to inform company strategy, including competitive intelligence, clinical challenges, and patient management trends.
- Participate in and contribute to cross-functional insight forums, ensuring insights from the field are shared and discussed with Medical Affairs, R&D, and other key internal stakeholders.
Support for Clinical Research and Evidence Generation
- Support evidence generation activities to identify and address data gaps within the medical strategy.
- Engage and collaborate with clinical development on clinical trial site identification and support for future and ongoing clinical trials.
- Support company-sponsored clinical trials and investigator-sponsored trials (IST) by identifying trial sites, providing scientific input, and facilitating partnerships with investigators.
- Serve as a subject matter expert to support clinical trial education and enrollment initiatives.
Congress and Advisory Board Engagement
- Represent the company at key medical congresses and scientific meetings, engaging in scientific exchange, gathering insights, and supporting congress activities.
- Partner with Medical Affairs to plan and execute advisory boards and other scientific activities, contributing to agenda setting, scientific content development, and post-meeting follow-up.
Field Excellence and Compliance
- Document all field activities in Veeva CRM in accordance with company policies and regulatory requirements, ensuring compliance with industry standards.
- Act as a mentor to junior MSLs and provide training on best practices in scientific exchange, insight generation, and territory planning.
- Contribute to territory planning, establishing objectives that support broader organizational goals and metrics for field excellence.
Desired Experience/Education and Personal Attributes:
- Advanced Degree such as MD, PhD, PharmD, NP/PA - required
- 5+ years of MSL, Medical Affairs, or Clinical Development experience within Oncology - required *strong preference to medical affairs experience in Oncology
- Existing relationships with institutions, practices, and/or hospitals in territory -required
- Strong broad-based scientific and pharmaceutical knowledge
- Proven experience as a Principal / Lead Oncology MSL, leading large-scale projects with significant impact on company objectives, demonstrating successful execution of strategic initiatives in HCP engagement, clinical research, and field excellence.
- Skilled in driving cross-functional collaboration, delivering high-quality scientific insights, and consistently achieving measurable outcomes aligned with corporate goals.
- Exceptional organizational and time management skills
- Strong interpersonal skills including excellent collaboration, verbal and written communication
- Computer proficiency in Excel, Word, PowerPoint, and Adobe®
- Ability to travel frequently (50-70%), including overnight travel
Regular travel will be required for this role.
About the Employer
About Syndax:
Syndax Pharmaceuticals is a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies. Highlights of the Company's pipeline include revumenib a highly selective menin inhibitor, and Niktimvo™ (axatilimab-csfr), a monoclonal antibody that blocks the colony stimulating factor 1 (CSF-1) receptor. Syndax is working to unlock the full potential of its pipeline and is conducting several clinical trials across the continuum of treatment for both revumenib and Niktimvo. For more information, please visit www.syndax.com/ or follow the Company on X (formerly Twitter) and LinkedIn.
Syndax Pharmaceuticals is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.
How to Apply
Please email your resume to Isabella Clemens iclemens@syndax.com or apply online
Contact Information
Isabella Clemens
35 Gatehouse Drive
ste D-3
Waltham, MA 02451 USA
https://syndax.com/
iclemens@syndax.com
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