Associate Medical Director - Oncology (West Coast)
Associate Medical Director - Oncology (West Coast)
Posted yesterday
SENIORITY
Lead
About the role
- Execute 8–12 MD-level engagements per quarter within defined geography, with at least 50% in pre-identified top strategic community accounts.
- Maintain at least 3 field ride days per month alongside MSL counterparts, targeting accounts designated by area leadership.
- Establish contact with medical leads in assigned top accounts; engage 100% of flagged accounts within 10 business days of assignment. Share responsibility for implementation and execution of “platinum-glove” provider engagement activities with area AMD lead. Scientific Communication and Education
- Attend, support, or present at regional educational programs as directed; develop toward independent program leadership over time.
- Complete annual recurrent speaker training; maintain working proficiency across assigned tumor histologies and the MRD diagnostic landscape.
- Document scientific exchange summaries and objection-handling themes in Salesforce following each engagement. Cross-Functional Collaboration
- Participate in bi-weekly 1:1s with MSL manager and attend monthly MSL team meetings; support area planning sessions as directed.
- Respond to escalated area medical inquiries within 48 hours with 100% closed-loop documentation; triage complex inquiries to the AMD or histology-specific Medical Directors.
- Generate at least 2 actionable regional insights per quarter; contribute to quarterly written insight report submitted to AMD or manager. Identify, triage and resolve operational issues coming from area accounts through cross-functional coordination and ownership. Clinical Development Support
- Identify and document field-driven evidence generation opportunities; escalate to AMD for evaluation and submission to histology lifecycle teams.
- Support AMD-led clinical trial concept development; participate in one histology-specific program identification per year. Performs other duties as assigned.
- M.D. or D.O. with board certification or active board eligibility in medical oncology, medical oncology/hematology, radiation oncology, surgical oncology or a directly related clinical specialty.
- Minimum 2–5 years of clinical practice or medical affairs experience following training (HM4 level; equivalent field experience accepted).
- Clinical knowledge across at least one or more tumor histologies and foundational understanding of molecular diagnostic testing in oncology.
- Demonstrated ability to communicate clinical data and engage physician audiences in a professional setting.
- Prior medical affairs, MSL, or field-based clinical role in oncology diagnostics, pharma, or biotech.
- Familiarity with cfDNA-based testing, MRD assays, or molecular residual disease concepts.
- Experience presenting at scientific or clinical educational forums. KNOWLEDGE, SKILLS, AND ABILITIESTechnical:
- Clinical knowledge across oncology histologies relevant to the assigned geography; capacity to develop proficiency in Natera's full product portfolio.
- Working proficiency in Salesforce or equivalent CRM for documentation and compliance adherence.
- Ability to interpret and communicate clinical data and study results to physician audiences. Behavioral:
- Developing autonomy. Executes within defined parameters; proactively seeks guidance when needed and builds toward independent problem-solving.
- Bias for action. Does not wait to be directed on routine field activities; moves on assigned priorities without prompting.
- Scientific curiosity. Asks questions, reads the data, and actively builds proficiency across the MRD landscape and Natera product evidence.
- Cross-functional awareness. Understands how medical affairs, MSL, commercial, and marketing functions interrelate and engages accordingly.
- Clear communicator. Can simplify complex clinical concepts for diverse physician audiences and internal stakeholders.
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