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Medical Affairs Professional - Oncology (Medical Advisor)

2-3 years
Not Disclosed
10 Dec. 24, 2024
Job Description
Job Type: Full Time Education: MBBS/MD/PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Join Our Team at Lilly

At Lilly, we combine compassion with innovation to improve lives across the globe. Headquartered in Indianapolis, Indiana, we are a global healthcare leader dedicated to discovering and delivering life-changing medicines. Our team of passionate employees works to enhance disease management, promote better understanding of health challenges, and give back to communities through volunteerism and philanthropy. Guided by a commitment to putting people first, we are searching for individuals who are determined to make a difference in the world.


Job Summary

The Medical Affairs Professional (MAP) serves as a therapeutically aligned Clinical Scientist within our Medical Affairs organization. This pivotal role involves leveraging deep knowledge of disease areas, available treatments, and investigational compounds to provide strategic and tactical leadership in lifecycle planning.

As a key partner to the Brand team, the MAP ensures alignment with external customer needs and internal business objectives. They also uphold compliance with global regulations, Good Clinical Practices, and Lilly's policies while supporting the affiliate’s medical and functional vision.


Key Responsibilities

Scientific Expertise and Medical Affairs Execution

  • Develop and contribute to therapeutic area medical plans in collaboration with the Clinical Research Physician (CRP).
  • Lead or support the development of scientific materials such as abstracts, posters, and manuscripts.
  • Collaborate with other Medical Affairs roles (e.g., CRP, CRS, MSL) to deliver outstanding customer experiences through educational initiatives, utilizing omnichannel tools where possible.
  • Gather insights on patient journeys, unmet needs, and treatment patterns in partnership with field medical teams.
  • Assist CRP in preparing and executing data generation plans that align with business needs.
  • Create and review medical information letters in collaboration with the Medical Information team.
  • Support scientific data disclosure (SDD) plans and serve as a scientific leader on research and regulatory deliverables.
  • Stay current on relevant medical literature, therapeutic developments, and emerging trends in clinical practice and access.

Cross-functional Collaboration

  • Serve as the primary medical contact for cross-functional teams, contributing clinical and scientific insights to strategic discussions.
  • Act as a key resource for medical support during product launches.
  • Oversee the medical components of local Patient Support Programs and internal training for business partners, such as Sales and Marketing teams.
  • Plan and implement symposia, advisory boards, and educational events for healthcare professionals.
  • Provide strategic recommendations for identifying consultants and external experts.
  • Collaborate effectively with alliance partners and internal stakeholders.

Customer Engagement and Experience

  • Respond to external inquiries and escalations in line with company policies.
  • Build and maintain relationships with Thought Leaders and professional societies.
  • Deliver scientific presentations and lead educational meetings, both virtually and in person.
  • Drive customer engagement improvements through digital innovations and take a leadership role in creating positive customer experiences.

Regulatory Collaboration

  • Contribute to the development and review of labeling and modifications alongside CRPs and regulatory teams.
  • Provide medical expertise for regulatory reports, agency meetings, and local registration efforts.
  • Participate in health authority meetings and risk management planning.

Professional Development

  • Stay informed through ongoing professional development and training.
  • Complete performance objectives (myPM) according to company guidelines.
  • Adhere to and ensure compliance with all company policies and procedures.

Qualifications and Skills

Education

  • Required: MBBS or PhD in a medically related field.
  • Preferred: MD in clinical or non-clinical specialties.

Experience

  • Required:
    • At least 2 years in a medical or scientific role within the pharmaceutical industry.
    • Proven ability to engage with customers and work across functions, including Marketing and Regulatory teams.
  • Preferred:
    • 2–3 years of relevant clinical practice experience.

Core Skills

  • Strong leadership and relationship-building abilities.
  • Capable of managing complex deliverables with effective prioritization.
  • Proficiency in interpreting scientific data for actionable communication.
  • Excellent interpersonal and communication skills.
  • High learning agility and business acumen.

Additional Requirements

  • Willingness to travel domestically and internationally as needed.
  • Availability for occasional evening or weekend work.

Why Join Lilly?

At Lilly, we celebrate diversity, foster inclusion, and ensure that every employee feels valued. We provide equal opportunities and are committed to creating an accessible and supportive environment for individuals with disabilities.

If you need assistance with the application process, please complete the Workplace Accommodation Form.

Join us in improving lives and making a lasting impact. Together, we can make life better for people around the world.

#WeAreLilly