出海雷达

Vice President, Clinical Development

其他限定地区(需当地身份)
公司Aura BioSearch
薪资未公开
工作地点United States
地域资格限定地区(需当地身份)
时区要求日间重叠约 9 小时,基本正常作息
用工类型Full Time
发布时间今天
数据来源Himalayas
前往 Himalayas 查看并投递 →
注意地域限制:该职位明确限定在 United States 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。
关于本页中文:职位描述由本机离线模型翻译,属机器翻译,供快速判断用;正式沟通与投递请以英文原文为准。官方翻译通道恢复后会自动重译升级。

澳门银河娱乐平台是我们在全球范围内领导的生物制药行业,专注于罕见疾病。我们的客户致力于对生活中影响到罕见病症的人生。他们的成功是由一个激情团队推动的,以满足罕见病患者独特需求,使工作既从事职业和个人来说都很有回报。他们目前正在寻找高技能人士,他们在活跃,快速的环境中繁荣,并与团队合作,进步改变罕见病的治疗方法。理想候选人将分享他们的使命和价值观,这些目标是专注于患者的关注,以及合作,他们追求改善全球患者的生活愿景。职位总结:我们的客户正在寻找临床发展副总统担任 CMO 的主要战略伙伴。这个角色将监督代谢和肿肿瘤学计划的战略规划和执行,同时领导跨功能项目战略团队由临床开发,运营,监管,CMC,医疗事务,商业和项目管理组成。副总理将负责制定和实施客户管道内项目临床开发和商业化全球战略,包括潜在的新计划。理想候选人应带来重要的临床发展专业知识,特别是病和罕见疾病,并拥有经验管理治疗疗法的整个生命周期从 IND 前到商业化,跨多种模式。关键责任:· 在所有方案中提供临床领导和战略方向。·领导对临床发展的全球战略计划进行成功商业化的发展。·提供核心疾病领域的深入知识和对未来发展,出版物和演讲的战略见解。· 提供监督并促进有关开发策略和风险的讨论。· 与董事会进行跨职业沟通,包括关于计划策略,风险和进展的沟通。·领导监管策略和 FDA 参与,包括定期向监管机构提交演示。·管理和指导团队,确保与战略目标和时间表保持一致。·与生物识别,监管,临床运营和医疗事务等关键部门合作;

查看英文原文

Aura Biosearch is conducting an executive search on behalf of our client, a global leader in the biopharmaceutical industry focused on rare diseases.
Our client is committed to making a significant impact on the lives of individuals living with rare conditions. Their success is driven by a passionate team driving for that meets the unique needs of rare disease patients, making the work both professionally and personally rewarding.
They are currently seeking highly skilled individuals who thrive in a dynamic, fast-paced, and collaborative environment to join their team in advancing life-changing therapies for rare diseases. The ideal candidate will share their mission and values, which are centered on patient focus, and collaboration, as they pursue their vision of bettering patients lives worldwide.
Position Summary:
Our client is searching for a Vice President of Clinical Development to serve as a key strategic partner to the CMO. This role will oversee the strategic planning and execution of the metabolic and nephrology programs, while leading cross-functional Project Strategy Teams composed of Clinical Development, Operations, Regulatory, CMC, Medical Affairs, Commercial, and Project Management. The VP will be responsible for developing and implementing the global strategy for clinical development and commercialization of programs in the clients pipeline, including potential new programs. The ideal candidate should bring significant expertise in clinical development, particularly in nephrology and rare diseases, and have experience managing the full lifecycle of therapeutics from pre-IND to commercialization, across multiple modalities.
Key Responsibilities:

  • Provide clinical leadership and strategic direction across all programs.
  • Lead the development of global strategic plans for clinical development towards successful commercialization.
  • Provide deep knowledge in core disease areas and strategic insights into future development, publications, and presentations.
  • Offer oversight and facilitate discussions on development strategies, risks.
  • Cross-functional communication, including with the board regarding program strategies, risks, and progress.
  • Lead regulatory strategy and FDA engagement, including regular presentations to regulatory agencies.
  • Manage and mentor teams, ensuring alignment with strategic goals and timelines.
  • Collaborate with key departments, including biometrics, regulatory, clinical operations, and medical affairs, to ensure cohesive program execution.
  • Develop and manage program budgets, timelines, and deliverables, ensuring strategic alignment and financial oversight.
  • Represent clinical development programs at scientific conferences and in discussions with regulatory agencies and KOLs.

Education/Experience Requirements:

  • MD (nephrologist preferred) with 12+ years of experience in pharmaceutical or biotechnology clinical development, including at least 6 years in a leadership role.
  • Extensive experience in clinical development across all phases, from pre-clinical through commercialization, including successful NDA/BLA submissions.
  • Strong leadership, negotiation, and communication skills with experience engaging various stakeholders.
  • Proven ability to lead cross-functional teams in a global environment, including experience with FDA and international regulatory bodies.
  • Willingness to travel domestically and internationally as necessary.

This is an exceptional opportunity to make a tangible impact in the rare disease space with an innovative and mission-driven biopharmaceutical company. If you possess the qualifications and passion for rare disease therapeutics, Aura Biosearch invites you to apply for this key leadership position on behalf of our client.
Originally posted on Himalayas

本页面信息整理自 Himalayas,版权归原发布方所有。职位可能随时关闭,投递请以原始页面为准。 本站只做信息聚合展示,不参与招聘流程,也不向求职者收取任何费用。

该公司其他在招职位

← 返回全部职位