AstraZeneca
AstraZeneca (LSE/STO/Nasdaq: AZN) is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines in Oncology, Rare Diseases and BioPharmaceuticals, including Cardiovascular, Renal & Metabolism, and Respiratory & Immunology. Based in Cambridge, UK, AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. Please visit astrazeneca.com and follow the Company on Twitter @AstraZeneca.
AstraZeneca Vietnam
As a Foreign Invested Enterprise with over 600 members, AstraZeneca is investing into Vietnam 360 million USD from 2020 to 2030 with a focus on reducing the burdens of non-communicable diseases, developing local talent, and uplifting the domestic biopharmaceutical R&D and manufacturing capabilities.
Over the last three decades accompanying Vietnam’s sustainable development, AstraZeneca has run several impactful programmes in collaboration with the Government, Ministry of Health and healthcare partners to promote disease awareness, prevention and early detection. In recent years, AstraZeneca Vietnam has received several certificates of merit from the Prime Minister and Minister of Health, for excellent contributions to Vietnam’s vaccine diplomacy, fight against COVID-19 and advancement of cancer treatment and disease awareness. The company has also been recognized among Vietnam’s Top 100 Best Places to Work (2018 – 2023) with various other industry awards from BritCham, EuroCham, and government agencies.
What You’ll Do
Job Description / Capsule
An internal and externally facing medical role that provides medical and clinical expertise in priority therapeutic/disease areas and builds AZ scientific leadership. Participates and contributes with medical and clinical expertise in design of LCM and Brand Strategy. Takes leadership in implementation of Medical Plan/ activities in alignment with Brand strategy. Ensures that the Medical Activities meet the needs of patients and customers. Engages Opinion Leaders in ESRs, scientific exchange meetings and advisory board meetings. Defines and delivers training on Medical background of the product or various functions in an organization. May take responsibility as Nominated Signatory medical reviewer for activities and promotional materials. May take responsibility for mentorship of MSL/s in the country. May lead Medical Information and Pharmacovigilance within a particular market.
Objectives
Critical actions
Measures (Quantitative – Qualitative – Attitudinal)
To establish AstraZeneca as a scientific leader through proactive, updated and effective Medical input
- Continuously acquire and update necessary scientific knowledge on therapeutic area and relevant compounds.
- Develop and implement the local medical plan to address unmet medical needs in priority disease areas and ensure alignment with the brand plan.
- Collaborate with MSL to seek input from MSL insights for development of local medical plan .
- Develop and implement pre-launch medical plan/activities for new products at least 2 years prior to the planned launch in the country to address key clinical and scientific challenges
- Provide medical leadership on faculty and content development for medical programmes including national congresses, advisory boards, scientific exchange meetings, publications, CMEs to meet identified needs
- To ensure that the Medical Information provided both to external and internal customers is timely, relevant, accurate and scientifically balanced
- Provide local medical expertise to local area/regional brand teams
- Provide medical input to phase 1 to 4 study protocols, study feasibility and support operational delivery
- Provide Medical expertise to support PSP market research, PASS and ESRO.
- Completion of the medical academy
- Number of reactive ESRO discussion
- Delivery of approved prelaunch medical plan in cooperate with local brand strategy
- Implementation of the prelaunch medical plan.
- Proactive update of medical knowledge in the internal meeting
- An approved Medical plan that is fully aligned with the Brand plan.
- Medical information should meet defined markets standards – time, quality in 5 days.
- 40% of time in field is required for engagement with the highest priority HCPs and key external stakeholders engagement
- Share emerging data with HCPs, discussing all aspects of the data in a scientific, objective and balanced way
- Disseminate results of studies completed to medical community by translating their clinical values and incorporating into business strategies
- Attend relevant scientific congresses and HCP meetings to gather new knowledge on AZ compounds, competitor information and therapeutic area
- Conduct professional scientific communication or presentation (become chairperson/presenter when necessary) with key opinion leaders (prominent
- Liaise with local investigators and the External Sponsored Research organization to support research initiatives.
- Internally communicate competitive intelligence
- Time in field versus plan
- Timeliness and actual number of achievements: P2P, 1:1 interaction, advisory board, publication, CME, responses to queries versus plan
- Market preparation of new launch product and/or pipeline among OLs.
- customer feedback post events/symposia
- Idea generation of the company sponsored clinical research
- Oversight and accountability of the operation of the studies
- Initiate research discussions, for example NIS, with customers to develop studies that will fulfil global and local business strategies. (May as part of the review team conduct initial assessment of any ISS proposals)Participate as key member of brand team as strategic partner towards LCM actions including potential business development opportunities
- Develop NIS or registry studies to address unmet medical needs.
- Developing partnership with OLs in order to develop their capabilities of conducting medical studies
- Number of discussion - NIS/IIS Proposals
- Oversight the all accountability of the operation of the studies, i.e. Milestones, quality and capacity of the study
- Timely publications of studies completed
- Initiatives with investigators to develop capabilities in conducting medical studies
- Support to develop drug value pack and communicate it to Key Decision Makers
- Support market access activities that shape market understanding of disease, diagnosis and treatment options
- Proactive crossfuctional collaboration with regulatory and other teams in drug registration in earlier and broader accessibility aligned to the brand strategy
- Number of communications to KDMs versus plan
- Meet the critical project timeline
- Feedback from crossfunctional team
- Provide effective Medical/clinical trainings (basic science and disease knowledge, drug profile, clinical data) to internal colleagues in line with expressed needs of MSL manager and sales managers:
- Ensures own knowledge and knowledge of team members of best practices and new relevant developments is up to date
- Percent completion of trainings conducted versus plan as per the business needs versus plan
- Feedback from participants ; facilitator effectiveness average more than 4 points
- MSL and MR competency in terms of disease knowledge, drug profile and clinical data (through MSL Accreditation)
- Accountable for ensuring Promotional Compliance: Provide medical input to the creation, development and agreement of promotional material and ensure all material is in line with internal SOPs and meets IFPMA code
- If appropriate to market, Ensure that Pharmacovigilance activities meet internal SOP and local regulations
- Ensure clinical studies are carried out in accordance with AZ SOPs and cGCP. Support Clinical team to select appropriate investigators and sites optimising quality, delivery and commercial benefit
- Aligns with the values and vision of AZ
- Actively participate/encourage the development of the AZ culture
- Ensures compliance with AZ code of conduct, Corporate Governance, Audits requirement, guidelines, codes, policies and procedures
- Ensures that company confidentiality is maintained (i.e. intellectual property, product, strategic and salary information)
- Discloses potential breach of codes or conducts
- Display behaviours consistent with the AZ vision and values (those with line report, their team members demonstrates the same)
- Feedback from others; climate survey
- No non-compliance issues raised with local and global policies and procedures
- No valid complaints from competitors against marketing practice
- No breach of confidentiality. All disclosures are investigated and resolved
- No critical finding in relevant internal or regulatory authority audits
- Develop functional capability in the role
- Communicate, develop and role model AZ culture and AZ Values & Behaviours
- Develop individual and team accountability
- Identify areas for self-development and discuss developmental needs with line manager using the 70-20-10 principle (experiential learning, coaching/networking/relationship-based learning and class room training)
- Attend & actively participate in learning programmes, training, projects and meetings (where needed)
- 100% completion of training as required on Medical Academy
- Feedback on congress report/highlights shared with cross- functional team as planned – completed feedback templates
- Having a personal development plan and completes identified development activities as planned Feedback from key stakeholders (optional)
Education, Qualifications, Skills and Experience
- A medical degree with specialization, or appropriate experience, in the required product or disease area
- Medical/Scientific knowledge in the responsible disease area
- Interest in a long-term career in the pharmaceutical industry
- Excellent presentation skills
- An ability to travel
- Fluency in English is required
- Qualified Doctor
- MSc/PhD in a scientific discipline
- Understanding of multiple aspects within Medical Affairs
- Knowledge of the latest technical and regulatory developments (essential for Sr MAM)
- Experience of Medical Affairs function within a pharmaceutical industry (essential for Sr MAM)
- Experience in relationship and stakeholder management
- (essential for senior MA)
- Project management experience
- Team management experience (essential for senior MAM)
Internal (to AZ or team)
- Senior Management within Brand or Disease area
- Medical Affairs Function
- Regulatory affairs
- Market access
- Marketing
- R&D team
- Compliance Team
- Service Providers
- Regulatory bodies
- Payor/reimbursement agency
- Other local and regional stakeholders
- Healthcare professionals
Be bold and make a powerful impact: AstraZeneca is a world-leading business where standards are high and challenges complex, but also a collective where we build, support and motivate each other. This unique combination of strong expectation and empowerment invites you to improve how our markets work and make your individual mark. Here, you can follow your ambitions with full confidence. As part of a responsible, value-led business with a strong sustainability agenda, you can also help impact the future beyond business projects.
Be part of our growth journey and success story: Join the fastest growing pharmaceutical company in our markets, set up to fuel further growth. Make the most of our assets: our strong heritage, our early investment and commitment in emerging markets, and how we embrace digital and data to transform the patient journey. Go beyond your limits. Welcome failure as a chance to learn. There’s no better place to feel inspired, energised and try new things.
Learn and grow by embracing diverse opportunities: Experience an organisation where professional development is prized and nurtured. Access the tools and support you need to continuously learn. Then it’s up to each of us to step up, speak up and show what we can do. Take advantage of working in a global business with opportunities to move beyond your role and open international doors. At AstraZeneca, your future is in your own hands.
Urgently bring our leading pipeline to millions of patients in need: Seize the opportunity to help improve the lives of millions of patients, including in areas where patient needs are often unmet. Work with our transformative pipeline to help bring a variety of high-quality medicines to market – and ensure they are made easily accessible to as many patients as possible.
Be heard in a culture of local empowerment: AstraZeneca is set up for creativity. We encourage unity and ownership at a local level, with collaboration across the global organisation. We tailor how we work, adapting to our markets and healthcare systems. In our diverse community, every voice is important. Share your ideas and opinions openly. In our speak-up culture, the way we communicate with each other leads to more powerful innovation.
So, what’s next?
If you are already inspiring yourself to join our dream team, we can’t wait to hear from you.
If you are ready to bring new insights and fresh thinking to the table, Brilliant! We have one seat available, and we hope it’s yours.
If you’re curious to know more then please take initiative to [email protected]. We encourage your application.
Where can I find out more?
Visit our website www.astrazeneca.vn
Follow us on LinkedIn www.linkedin.com/company/astrazeneca/ and Facebook https://www.facebook.com/AstraZenecaVN
Contact us via [email protected]
Nha khoa Tâm Đức Smile được thành lập từ tháng 4 năm 2008. Sau hơn 11 năm hoạt động, trung tâm đã tạo dựng được uy tín và sự tin cậy từ phía khách hàng, dần khẳng định được vị thế của mình trong những trung tâm chăm sóc răng miệng hàng đầu Việt Nam, chuyên về cấy ghép Implant và răng sứ thẩm mỹ.
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Với đầy đủ giấy tờ pháp lý, bằng cấp và bề dày kinh nghiệm của đội ngũ bác sĩ, hệ thống trang thiết bị tiên tiến và sử dụng công nghệ hiện đại chuẩn quốc tế như: Máy X Quang Conebeam CT 3D, máy Panorex – Cephalometric, công nghệ thiết kế răng sứ CAD/CAM 3D, máy in mẫu răng hàm mặt 3D, phần mềm phân tích Implant 3D, công nghệ VCeph 3D, máy tẩy trắng răng Laser thế hệ mới…
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