Job Description Summary
#LI-Hybrid
This role is based in Taipei Taiwan. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
Aligned with the overall product strategy the Medical Advisor plays a pivotal role in shaping and executing Medical Affairs plans for the assigned Therapy Area. This includes driving scientific excellence supporting the design and implementation of clinical studies and fostering meaningful educational dialogue with Key Opinion Leaders (KOLs) and regulatory stakeholders. By delivering trusted scientific information and insights the Medical Advisor helps advance innovative therapies that improve patient outcomes and contribute to Novartis mission of reimagining medicine.
Job Description
Key Responsibilities:
Respond to medical inquiries promptly and accurately ensuring compliance with internal standards and regulatory requirements; develop standard response documents for frequently asked questions.
Provide scientific and medical input into clinical trial and research activities including initiation oversight and execution of studies within the therapeutic area.
Support Non-Interventional Studies (NIS) and Investigator-Initiated Trials (IITs) by guiding strategy feasibility and governance processes.
Review and approve medical and promotional materials ensuring alignment with local regulations P3 guidelines and tailoring global/regional content for local stakeholder engagement.
Deliver actionable medical insights to cross-functional teams (e.g. Pharmacovigilance Regulatory Affairs Market Access QA Commercial Brand) to inform strategy and decision-making.
Ensure compliance and risk management including identification mitigation planning and implementation of internal controls within assigned responsibilities.
Lead scientific engagement initiatives such as educational programs advisory boards and congress activities to strengthen external stakeholder relationships.
Contribute to medical governance and training ensuring adherence to ethical standards and supporting internal teams with scientific expertise.
Essential Requirements:
Proven ability to work closely with Medical Affairs Clinical Market Access Regulatory and Commercial teams to align medical strategies with business objectives.
Strong analytical skills to gather and translate medical insights into actionable strategies. Excellent written and verbal communication skills for engaging internal and external stakeholders.
Familiarity with local and global regulatory requirements medical governance standards and promotional material review processes.
Solid understanding of therapeutic areas clinical trial design and evidence-based medicine. Ability to interpret and communicate complex scientific data effectively.
Advanced degree in life sciences or healthcare; Pharmacy Doctorate or MBBS strongly preferred. Additional qualifications in pharmacology clinical research or related fields are an advantage.
Skills Desired
Building Constructions Clinical Protocols Clinical Research Clinical Trials Drug Development Hazard Identification (HAZID) Health Sciences Immunology Intensive Care UnIT (Icu) Internal Controls Internal Medicine Internet Protocol Suite Job Description Medical Information Organizing Patient Care Stakeholder Engagement Utilization Management (Um)
Required Experience:
Unclear Seniority
Job Description Summary#LI-HybridThis role is based in Taipei Taiwan. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.Aligned with the overall product strategy the Medical Advisor plays a pivotal role in shaping and executing Med...
Job Description Summary
#LI-Hybrid
This role is based in Taipei Taiwan. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
Aligned with the overall product strategy the Medical Advisor plays a pivotal role in shaping and executing Medical Affairs plans for the assigned Therapy Area. This includes driving scientific excellence supporting the design and implementation of clinical studies and fostering meaningful educational dialogue with Key Opinion Leaders (KOLs) and regulatory stakeholders. By delivering trusted scientific information and insights the Medical Advisor helps advance innovative therapies that improve patient outcomes and contribute to Novartis mission of reimagining medicine.
Job Description
Key Responsibilities:
Respond to medical inquiries promptly and accurately ensuring compliance with internal standards and regulatory requirements; develop standard response documents for frequently asked questions.
Provide scientific and medical input into clinical trial and research activities including initiation oversight and execution of studies within the therapeutic area.
Support Non-Interventional Studies (NIS) and Investigator-Initiated Trials (IITs) by guiding strategy feasibility and governance processes.
Review and approve medical and promotional materials ensuring alignment with local regulations P3 guidelines and tailoring global/regional content for local stakeholder engagement.
Deliver actionable medical insights to cross-functional teams (e.g. Pharmacovigilance Regulatory Affairs Market Access QA Commercial Brand) to inform strategy and decision-making.
Ensure compliance and risk management including identification mitigation planning and implementation of internal controls within assigned responsibilities.
Lead scientific engagement initiatives such as educational programs advisory boards and congress activities to strengthen external stakeholder relationships.
Contribute to medical governance and training ensuring adherence to ethical standards and supporting internal teams with scientific expertise.
Essential Requirements:
Proven ability to work closely with Medical Affairs Clinical Market Access Regulatory and Commercial teams to align medical strategies with business objectives.
Strong analytical skills to gather and translate medical insights into actionable strategies. Excellent written and verbal communication skills for engaging internal and external stakeholders.
Familiarity with local and global regulatory requirements medical governance standards and promotional material review processes.
Solid understanding of therapeutic areas clinical trial design and evidence-based medicine. Ability to interpret and communicate complex scientific data effectively.
Advanced degree in life sciences or healthcare; Pharmacy Doctorate or MBBS strongly preferred. Additional qualifications in pharmacology clinical research or related fields are an advantage.
Skills Desired
Building Constructions Clinical Protocols Clinical Research Clinical Trials Drug Development Hazard Identification (HAZID) Health Sciences Immunology Intensive Care UnIT (Icu) Internal Controls Internal Medicine Internet Protocol Suite Job Description Medical Information Organizing Patient Care Stakeholder Engagement Utilization Management (Um)
Required Experience:
Unclear Seniority
View more
View less