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Medical Lead Oncology

2+ years
Not Disclosed
10 Sept. 23, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Summary

In alignment with our overall product strategy, the Medical Advisor plays a crucial role in supporting the design, implementation, and execution of Medical Affairs plans for the assigned therapy area. This position involves providing scientific information, assisting in the design and organization of clinical studies, and fostering educational dialogues with key opinion leaders (KOLs) and regulatory stakeholders.

About the Role

Key Responsibilities:

  • Support the country medical affairs strategy in line with global initiatives, market insights, and local conditions, implementing Medical Affairs activities within designated therapy areas.

  • Coordinate scientific meetings, symposia, congresses, and Continuous Medical Education (CME) events, creating engagement plans for customer-facing activities to ensure timely and compliant execution.

  • Ensure high-quality, timely responses to inquiries in accordance with applicable standards; develop response documents for frequently asked questions.

  • Provide medical and scientific input for clinical trial activities, including the initiation and oversight of studies, and support strategies for Non-Interventional Studies and Investigator Initiated Trials.

  • Manage the review and approval of medical and promotional materials, ensuring they are tailored to local needs and comply with local guidelines.

  • Share medical insights with cross-functional teams, including Pharmacovigilance, Regulatory Affairs, Market Access, Quality Assurance, and Commercial teams.

  • Identify and assess risks within the area of responsibility, developing mitigation plans and monitoring internal controls.

Essential Requirements:

  • Education: MBBS or MD is mandatory, with a minimum of 1+ years of industry experience.

  • Skills:

    • Operations management and project execution.
    • Collaborative skills across boundaries.
    • Knowledge of clinical trial design and medical science.
    • Expertise in medical education and scientific engagement.
    • Familiarity with Non-Interventional Studies (NIS) and epidemiology studies.
    • Understanding of medical governance and safety protocols.

Desirable Requirements:

  • Knowledge in the cardiovascular field is preferred.

Why Novartis?

Our purpose is to reimagine medicine to enhance and extend lives. We aim to be the most valued and trusted medicines company in the world, and our associates are the driving force behind this mission. Join us in our commitment to improving patient lives globally.

Commitment to Diversity and Inclusion

Novartis is dedicated to creating an inclusive work environment that reflects the diversity of the patients and communities we serve.

Accessibility and Accommodation

We are committed to providing reasonable accommodations for individuals with disabilities. If you need assistance during the recruitment process or to perform essential job functions, please contact us at diversityandincl.india@novartis.com, including the job requisition number in your message.

Join Our Novartis Network

If this role doesn’t align with your experience or career goals, but you want to stay informed about future opportunities, join the Novartis Network here.

Benefits and Rewards

To learn more about our comprehensive benefits and rewards, please refer to the Novartis Life Handbook here.


Join us at Novartis, where your expertise can contribute to breakthroughs that change patients’ lives!