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(Sr) Medical Advisor-Rlt

2+ years
Not Disclosed
10 Dec. 14, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Here’s a refined version of the Medical Advisor role at Novartis:


Position: Medical Advisor

Location: Shanghai, China
Division: International | Innovative Medicines
Company: Novartis Pharma Co., Ltd


About Novartis

Novartis is dedicated to improving the quality of life for patients by driving breakthroughs in science. With a global team of passionate individuals, we combine cutting-edge innovation with a collaborative spirit to tackle the world’s toughest health challenges.


About the Role

The Medical Advisor plays a crucial role in supporting the design, execution, and implementation of Medical Affairs strategies for a designated therapy area. You will provide scientific input, help design clinical studies, and engage with key stakeholders, including KOLs and regulatory bodies, ensuring high-quality medical services that align with both local and global objectives.


Key Responsibilities

  • Medical Affairs Strategy: Support the country medical affairs strategy in alignment with global strategies, local insights, and market conditions.
  • Medical Engagement: Coordinate scientific meetings, congresses, and CME activities to foster scientific exchange and enhance therapy area engagement.
  • Medical Enquiries: Respond promptly and accurately to medical inquiries, ensuring high-quality, compliant answers, and developing standard response documents.
  • Clinical Trials & Research: Contribute to the development and execution of clinical trials and other research activities in the designated therapy area, supporting non-interventional studies and Investigator Initiated Trials.
  • Material Review: Oversee the review and approval of medical and promotional materials, ensuring compliance with local guidelines.
  • Cross-functional Collaboration: Provide medical insights to cross-functional teams such as Pharmacovigilance, Regulatory Affairs, Market Access, and Commercial teams.
  • Risk Management: Identify risks and develop mitigation plans to ensure compliance and quality within the area of responsibility.

What You’ll Bring to the Role

  • Education & Qualifications: Master’s degree or higher in a medical field
  • Languages: Fluent in English and Chinese
  • Experience:
    • Prior experience in medical advisory and new product launches preferred
    • Expertise in project management, operations, and execution within the pharmaceutical industry
  • Skills:
    • Strong collaboration and cross-functional teamwork capabilities
    • Ability to manage multiple priorities and drive successful outcomes
    • Expertise in clinical trial management and medical materials review

Why Novartis?

At Novartis, we work together to help patients and their families with innovative science and compassionate care. Our dynamic culture promotes collaboration, support, and breakthrough thinking to achieve meaningful results.


Benefits and Rewards

Explore the comprehensive benefits that help you thrive both professionally and personally. Visit Novartis Careers to learn more.


Equal Opportunity Employer

Novartis is committed to providing equal opportunities to all candidates, including those with disabilities. We offer reasonable accommodations to assist individuals during the recruitment process and in performing job functions. Please contact diversityandincl.china@novartis.com if you need any assistance.


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Let me know if you would like any additional changes or details!