Support development and execution of patient-focused medical strategies that maximize the value proposition of Amgen's therapies including annual strategic planning and goal setting, launch support and lifecycle management, in collaboration with Medical Head, appropriate cross-functional teams and governance
Contribute to cross functional stakeholder teams in shaping the healthcare ecosystem by enabling access to medicines through evidence generation, communication and education of medical and economic value
Synthesize and integrate insights to deliver medical inputs into relevant cross-regional/functional strategies, including relevant brand strategy
Foster and enhance collaboration and coordination across Medical
Contribute to strategy development for scientific engagement across a broad range of stakeholders to strengthen external understanding of the unmet need and value of the product
Lead/support relationships with external healthcare community, including interactions with opinion leaders, payers and societies for scientific exchange, where appropriate
Develop/support and lead/support execution of the strategy for medical evidence generation that shapes our products and informs the practice of medicine ensuring key needs are met in alignment with global product medical and relevant brand strategy
Foster Amgen‘s reputation as a science-based, innovative and patient-focused reliable partner
Develop and/or contribute to execution of advocacy plans and strategies in partnership with internal stakeholders and lead relationships as appropriate
May develop and manage medical product budget
Ensure conduct of medical activities in full compliance of all laws, regulations and SOPs
Ensure product/disease state/pipeline specific medical training where appropriate, may deliver training to others
Ensure appropriate clinical trial conduct as a key medical interface in close partnership with Global Development Operations (eg Site Management)
Provide strategic input into labels/regulatory/reimbursement/policy/promotional used to support internal/external interactions
Determine scientific/medical subject matter appropriateness of labels/regulatory/reimbursement/policy/promotional and medical deliverables (eg, slide decks, publications, educational activities) used to support internal/external interactions via appropriate review process
Contribute to strategy development for, review, approve and ensure dissemination of, medical communications and related activities (eg, product narrative, scientific platform, core content, publications including FPR/FLR, medical education and congresses)
Provide support and leadership of advisory boards and other relevant meetings (eg, investigator meetings, and/or expert panels)
Understand the expectations of key external stakeholders to support appropriate access to Amgen therapies.
In partnership with cross-functional team, ensure informed budget/resource trade-offs, as appropriate
Facilitates Investigator Sponsored Studies through Amgen governance and manage study lifecycle (including communicating with investigators, as appropriate and ensuring accurate reporting of key milestone data)
Contribute to lifecycle management plan
Minimum Requirements
Medical Degree or equivalent
Min of 2 years of medical affairs experience in pharmaceutical or biotechnology company in Saudi Arabia
Preferred Requirements
Demonstrated ability as a medical expert in a complex matrix environment
Pharmaceutical product development, product lifecycle and commercialization process knowledge with understanding of other functions; including, but not limited to, Clinical Operations, Commercial, Safety, Regulatory, Value & Access, and Medical Affairs
Experience in local medical practice and healthcare ecosystems
Skilled at engagement, scientific exchange with external medical community
Clinical research experience
In-depth understanding of the scientific method and clinical applications based on medical, scientific and practical rationale
Knowledge of Good Clinical Practices (GCP), SFDA regulations and guidelines, and applicable international regulatory requirements
Familiarity of local pharmaceutical industry and legal/health system environment
Skilled at effectively presenting ideas and documenting complex medical/clinical concepts in both written and oral communication
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