Novartis Saudi Arabia | نوفارتس السعودية
Medical Manager
Riyadh, Saudi ArabiaPosted 2 days ago
- Salary
- AED 12k–18k a month· est.
- Job type
- Full time
- Level
- Junior
- Field
- Healthcare & Medical
- Work mode
- On site
About the role
Summary In line with overall product strategy, the Medical Manager is a customer-facing responsible for supporting the design, implementation and execution of Medical Affairs plans for assigned Therapy Area, providing scientific information, helping design & organize clinical studies, building educational dialogue with MEs and regulatory stakeholders. About The Role Key Responsibilities: • Respond to medical enquiries accurately, compliantly, and in a timely manner, including developing standard response documents where needed. • Provide medical and scientific input into clinical trial and research activities, including study initiation and oversight within the therapy area. • Support local evidence-generation activities, including non-interventional studies and investigator-initiated trials. • Build scientific partnerships across the disease journey by engaging medical experts, supporting publications, and contributing to data generation initiatives. • Review and approve medical and promotional materials in line with local and global compliance requirements. • Share actionable medical insights with cross-functional stakeholders including Pharmacovigilance, Regulatory, Market Access, Quality, and Commercial teams. • Role involves 50% external stakeholder engagement and 50% office-based responsibilities. Requirements • Degree in MD, PharmD or PhD • Minimum 2 years’ experience in Medical Affairs in pharmaceutical industry, specific experience in Neuroscience is a plus • Proven ability to build credible relationships with medical experts and key decision-makers. • Strong understanding of clinical research, evidence generation, and the evolving therapeutic landscape. • Experience translating scientific insights into meaningful cross-functional action. • Confidence using digital tools and data to support stakeholder engagement, insight gathering, and decision-making. • Excellent communication, presentation, and collaboration skills in a matrix environment. • Fluency in both Arabic and English languages Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)
Requirements
- Degree in MD, PharmD or PhD
- Minimum 2 years’ experience in Medical Affairs in pharmaceutical industry, specific experience in Neuroscience is a plus
- Proven ability to build credible relationships with medical experts and key decision-makers.
- Strong understanding of clinical research, evidence generation, and the evolving therapeutic landscape.
- Experience translating scientific insights into meaningful cross-functional action.
- Confidence using digital tools and data to support stakeholder engagement, insight gathering, and decision-making.
- Excellent communication, presentation, and collaboration skills in a matrix environment.
- Fluency in both Arabic and English languages
Responsibilities
- Respond to medical enquiries accurately, compliantly, and in a timely manner, including developing standard response documents where needed.
- Provide medical and scientific input into clinical trial and research activities, including study initiation and oversight within the therapy area.
- Support local evidence-generation activities, including non-interventional studies and investigator-initiated trials.
- Build scientific partnerships across the disease journey by engaging medical experts, supporting publications, and contributing to data generation initiatives.
- Review and approve medical and promotional materials in line with local and global compliance requirements.
- Share actionable medical insights with cross-functional stakeholders including Pharmacovigilance, Regulatory, Market Access, Quality, and Commercial teams.
- Role involves 50% external stakeholder engagement and 50% office-based responsibilities.
Skills
- Medical Affairs
- Clinical trial input
- Non-interventional studies
- Investigator-initiated trials
- Scientific communications
- Medical publications
- Regulatory compliance
- Pharmacovigilance collaboration
- Cross-functional collaboration
- Data-driven stakeholder engagement
- Arabic and English bilingual communication
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