Intercontinental Medical Director, Oncology

Employer
Amgen
Location
Thousand Oaks, California
Posted
Oct 02, 2018
Ref
R-64013
Discipline
Science/R&D, Oncology
Required Education
Bachelors Degree
Position Type
Full time

We are building upon our solid oncology foundation and long-term commitment to patients by developing a whole new class of novel molecules - and we need top talent to ensure these molecules become medicines and realize their potential for helping patients.

To support our efforts we are hiring a Intercontinental Region Medical Director and TA Head for Oncology/Hematology, Biosimilars. In this role you will drive the development and execution of TA medical strategies to maximize Amgen's value proposition of in-line and pipeline products in alignment with global medical and brand strategies. In this role, the TA Head will partner very closely with the Global Development organization and the commercial and access Oncology Regional Leads to prepare for the launches of new products, both in hematology and solid tumor, as well as establish a close partnership with the affiliate medical leads to ensure proper global to affiliate alignment for the commercial portfolio. The TA Head is a member of the leadership team for the Intercontinental Medical organization.

  • Accountable for the development and execution of regional TA medical strategies including launch support and lifecycle management, in collaboration with Product Team/Portfolio governance and alignment with Global Medical strategy
  • Ensure strategic alignment within regional Medical teams and cross functional stakeholders
  • Accountable for the development of regional evidence generation strategy and study execution across Oncology/Hematology TA
  • Provide Oncology/Hematology and Biosimilars medical expertise on clinical content and scientific messages across publications and materials
  • Partner with Global Regulatory Affairs and Safety (GRAAS) in risk management/minimization activities
  • Collaborate with cross functional leadership in the Brand Planning Process to ensure alignment
  • Provide strategic input into development of advocacy plans and strategies in partnership with internal stakeholders
  • Accountable for budget planning and execution within Oncology/Hematology and Biosimilars TA
  • Accountable for maintaining and initiating Tier 1 expert networks throughout the region with clear deliverables
  • Travel internationally 20-30% of time

Key Activities:

  • Accountable for delivery of regional inputs to Global Medical Strategic Framework(s)
  • Ensure development of stakeholder mapping and Scientific Engagement Plan strategy
  • Regional accountability for clinical trial conduct within Oncology/Hematology TA
  • Provide medical input into Global Development strategies
  • Develop and maintain relationships with external healthcare community, including interactions with opinion leaders, payers and societies for scientific exchange
  • Provide strategic input into regional medical communication and education activities
  • Provide strategic input into data interpretation, analysis and communication
  • Medical input into label and regulatory interactions
  • Recruitment, retention, coaching, mentoring and developing departmental staff
  • Provide Oncology/Hematology and Biosimilar medical training
  • Ensure Oncology/Hematology TA compliance adherence
  • Ensure close collaboration and partnership with Site Management
  • Ensure patient-centered focus across all activities
  • Member of Regional Medical Leadership Team to help drive regional medical vision and strategy
  • Gather and synthesize insights to inform Regional and Global Strategy

Basic Qualifications:

  • MD or PhD with proven track record of leading teams
  • Two (2) or more years of clinical research experience and/or basic science research
  • Two (2) or more years in clinical research/medical affairs experience in biopharmaceutical industry (biotech or pharmaceutical)

Preferred Qualifications:

  • MD plus accredited fellowship in Oncology/Hematology, board certified or board eligible
  • Five (5) or more years of clinical research experience and/or basic science research combined with clinical teaching and patient care activities
  • Five (5) or more years of clinical research/medical affairs experience in the biopharmaceutical industry (biotech or pharmaceutical)

Experience:

  • Experience with clinical study management and conduct
  • Experience with developing and executing Medical Affairs strategies
  • Familiarity with health care compliance considerations
  • Experience with opinion leader interactions
  • Experience with payer and provider organizations
  • Broad and formal leadership experience including staff management