我们坚信每个人都值得拥有健康的生活 远离疾病且充满无限可能 我们将看到一个充满治愈力量的世界 如今那些选择有限的人可以体验各种可行的治疗方案 我们设想为医生 药剂师和护士提供新技术 这些技术不仅能够治疗慢性病 而且在预防慢性病方面也卓有成效 我们正在寻找有动力学习 成长和创新的团队成员 同时为全世界数百万人带来意义非凡的改变
The Medical Director will participate in the development of the Global Business strategy to explore-expand new medical use or markets.
This Medical Director will provide Medical perspective and expertise in the therapeutic applications of products and will play a key leadership role in the review and oversight of Investigator Initiated Trials globally.
The Medical Director will also build the scientific support and foundation and KOL network for the launch of products. The Medical Director is accountable and takes ownership of clinical research trial results and critically evaluates Investigator Initiated Studies (IIS) proposals.
This includes responding to adverse effects surfaced by internal or external quality reviews, determining if corrective action is required as well as directing, managing and ensuring corrective actions are applied successfully.
The Medical Director will need experience with clinical trials as well as sound grounding in Biostatistics and Regulatory Affairs to support the Therapeutic Area Leader activities, as needed, in clinical development including label changes, evaluation of product complaints and adverse events in conjunction with these specialty functions.
This Medical Director will need to develop and maintain strong scientific and medical relationships with Key Opinion Leaders (KOL’s).
Works with sales and marketing to identify KOL’s and supervise the educational and informational priorities for the therapeutic area.
Essential Duties and Responsibilities :
Lead the development and implementation of a Medical Affairs clinical and education strategy. Drive the development of rational strategic plans for future clinical studies.
Act as Medical Monitor for clinical research studies. Capable of developing communications plan, including publication plans for therapeutic area.
Continuously develop and maintain "state of the art" level of knowledge as to developments and trends in medical sciences, especially in the designated therapeutic areas.
Provide expertise related to the evaluation and reporting issues and adverse events in conjunction with pharmacovigilance, as directed by the Therapeutic Area Leader.
Including the review of all adverse clinical consequences or complaints that could have led to an adverse clinical consequence and determine if corrective actions are necessary.
Strengthen relationships and develop new relationships with KOL’s in business selected therapies segments.
Continuously develop knowledge of regulatory, pharmacovigilance, and quality assurance requirements in alignment with Baxter Global Business Practice Standards.
Ensure compliance with all Business Policies and Guidelines in accordance with the OIG (for US staff).
Education and / or Experience :
MD degree, preferably with specialty training, (e.g. internal medicine, ideally in combination with an intensivist specialty) or equivalent training or experience.
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