【Alexion Japan】Medical Lead, HPP, GMT TA, Medical Affairs

This is what you will do:

HPPMedical Lead, associate director,is responsible to develop a medical plan/strategy, which plays pivotal role in medical activities of Alexion Medical Affairs, and to carry out with MSLs and the other Medical teams (Patient Program, HEOR, Evidence Generation Lead, Digital Lead, Publication Lead, Medical Communication, Medical Operation, Patient Advocacy). Medical strategy/plan must incorporate complex nature of disease and pathophysiology, medical and social system, trends and changes in science and medical practice, deep understanding of patients and patient journey, to elucidate true unmet needs and solutions. Coping with the key opinion leaders and other external stakeholders to execute the medical planinhigh standards effectively and efficientlyis required.

Sophisticated medical plan/strategyenablesachieving the objectivesthrough Scientific Exchange (SE) and medical activities, such as, but not limited to, evidence generation, medical education, publication, presentation at academic congresses, advisory board, and utilizing digital tools.The relationship constructed with medical KOLs and related academic societies are key for successful executionand maximizing the potential of the products for patients.Evidence generation and publication isparticularly important as solid deliverables from medical.

The abilities required to carry out the duties include sophisticated knowledge of medicine and pharmacy, relevant knowledge including medical system, scientific and logical mindset, ability to carry out works in timely manner, communication skills, negotiation skills, and morality.Adherence to AZ Value and Behavior is must for success.

You will be responsible for:

• Development and implementation of medical strategy and tactics in alignment with cross-functional partners and global counterpart

• Responsible in the launch preparation of on-going late stage project in collaboration with global medical affairs. 

• Strong leadership and contribution in the cross-functional launch team in independent manner is strongly expected

• In collaboration with MSL manager, develop and maintainmedical KOL lists and communication plan, which aligned with medical and cross-functional brand plan

• Planning and implementation of MA events such as advisory board, medical educations,i.e.Stand-alone medical symposium, webinars, congress medical events and presentation, videoand other medical activities

• Planning and promotion of Company Sponsored Research (CSR) and Externally Sponsored Research (ESR), particularly Externally Sponsored Collaboration (ESC) to address unmet needs and barrier in standard of care in collaboration with Evidence Generation lead and HEOR. Utilizing PMS and other data source creatively to maximize evidence generation is highly expected.

• In collaboration with Publication lead, drive high quality publications of aforementioned evidence generations, encore presentations, case reports.

• Planning and implementing Patient Support Program (PSP) and Patient Medical Programsin collaboration with Patient Program,Patient Advocay and other functions. Seek future opportunities to develop data from such PSP.

• Working with MSL managers to collect unmet medical needs and potential needs through interviews with health professionals, preparing reportsand sharing them with related departments to further improve medical plan.

• Providing education and lecture slide review with the aim of carrying out appropriate company activities and message

• Develop publication plan in collaboration with Publication lead, Evidence Generation Lead, HEOR, R&D,PMS and drive execution.

• Support Medical Communication (Medical Information) to develop FAQ and answers to unsolicited medical requests

You will need to have:

• As an Associate Director, self-driven and independence to plan and execute medical activities are indispensably required. Leading positive and enthusiastic team culture by demonstratingcollaborative and inclusiveattitudes with perseverance, contributing effective and efficient work process, developing constructive and collaborative relationship with other departments are highly desired. 

• Leadership skills to drive high quality work and motivation within teamisrequired.

• Minimum of 5 years of Medical Affairs in the pharmaceutical or the biotech industry (or experience with biological product).

• Master’s degree, PharmD, Ph.D in sciences, or MDbackground is highly desired.

• Unflagging enthusiasm to improvepatient care and to maximize the appropriate use of the products and sufficient knowledge of medical affairs work to efficiently execute medical activities to improve standard of care.

• Effective communication skills (written, verbal and presentation) both in local language and English sufficient to communicate with global counterparts Analytical skills as applied to medical, scientific and technical information

• Ability to evaluate medical/scientific literature and develop effective medical strategies and communication strategies accurately and effectively

• Travel required up to 20%

• Must be a strong team player, but at the same time, ability to work independently

• Good understanding of industry compliance practice and strong adherence to it

We would prefer for you to have:

• Background/experience with rare diseases, genetic diseases, metabolic diseases

• Preference for MBA, MD or professional certification, etc. definitely plus

• Ability to influence important customers, challenge common perceptions and implement medical affairs tools to improve patient care and outcomes

• Experience of early and late clinical development

• Ability to cope with high pressure and stress

• Adaptability to multicultural environment

• Identify priorities and managing deliverables

• Keeping composure under intense situations

• Flexibility and ability to adapt to changing conditions

• Excellent problem solving, organizational, and negotiating skills