远程工作雷达

全球临床研究高级总监 - ITP

Sr. Director, Global Clinical Research - ITP

职能支持限定地区(需当地身份)
公司Baxter International Inc.
薪资$224,000 - $308,000/年
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
发布时间昨天
数据来源Himalayas
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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。

这是你的工作产生影响的地方。
在Baxter,我们相信每个人——无论他们是谁或来自哪里——都应有机会过上健康的生活。这是我们1931年创立时的信念,也是我们持续遵循的指导原则。我们正在重新定义医疗交付方式,以在今天、明天以及未来产生更大的影响。
我们的Baxter同事因拯救和延续生命这一使命而团结在一起。我们的社区由勇气、信任和协作的文化驱动。每个人都被赋予了承担责任并产生有意义影响的能力。我们追求高效且有效的运营,并对彼此在实现卓越成果方面保持问责。
在这里,你找到的不仅仅是工作——还有目标和自豪感。
你在Baxter的角色:
高级总监,临床研究 - 输注治疗与技术负责将医学、临床和商业优先事项转化为可执行的证据生成策略,涵盖Baxter的ITP产品组合,包括药品、营养疗法、输注系统、药房技术和药物输送解决方案。
与医学事务部门紧密合作,高级总监将未满足的医学需求和战略证据优先事项转化为科学严谨的研究计划,能够生成具有意义的临床、经济和操作性证据,以支持创新、产品开发、监管提交、上市后证据生成、临床实践采用和基于价值的医疗倡议。该职位在研究方法、证据策略、研究治理、科学解释和跨职能执行方面提供领导力。
高级总监与医学事务和临床运营部门合作,确保研究项目在科学上可靠、在操作上可行、符合监管期望,并能够生成推动患者护理和业务目标的证据。
你将从事的工作:
临床研究策略与证据规划

  • 与医学事务部门合作,将医学证据优先事项转化为综合的临床研究策略。
  • 设计解决未满足的临床、科学、医疗系统和客户需求的证据生成计划。
  • 开发适合用途的研究设计。
  • 制定生成对临床医生、监管机构、支付方、提供者和健康系统相关证据的研究计划。
查看英文原文

This is where your work makes a difference.
At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.
Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.
Here, you will find more than just a job—you will find purpose and pride.
Your Role at Baxter:
The Senior Director, Clinical Research - Infusion Therapies & Technologies serves as the scientific leader responsible for transforming medical, clinical, and business priorities into executable evidence-generation strategies across Baxter's ITP portfolio, including pharmaceuticals, nutrition therapies, infusion systems, pharmacy technologies, and medication delivery solutions.
Working in close partnership with Medical Affairs, the Senior Director translates unmet medical needs and strategic evidence priorities into scientifically rigorous research programs capable of generating meaningful clinical, economic, and operational evidence to support innovation, product development, regulatory submissions, post-market evidence generation, clinical practice adoption, and value-based healthcare initiatives. The role provides leadership in study methodology, evidence strategy, research governance, scientific interpretation, and cross-functional execution.
The Senior Director works with Medical Affairs and Clinical Operations, ensuring that research programs are scientifically sound, operationally feasible, aligned with regulatory expectations, and capable of generating evidence that advances patient care and business objectives.
What you'll be doing:
Clinical Research Strategy & Evidence Planning

  • Partner with Medical Affairs to convert medical evidence priorities into integrated clinical research strategies.
  • Design evidence-generation programs that address unmet clinical, scientific, healthcare system, and customer needs.
  • Develop fit-for-purpose study designs.
  • Establish research plans that generate evidence relevant to clinicians, regulators, payers, providers, and healthcare systems.

Scientific Leadership

  • Serve as the organization's leading expert in clinical research methodology and scientific study design.
  • Ensure appropriate application of epidemiology, biostatistics, implementation science, health-services research, and clinical study methodologies.
  • Provide scientific oversight for protocols, statistical plans, clinical study reports, and evidence interpretation.
  • Ensure scientific rigor across all clinical research activities.

Clinical Operations Leadership

  • Lead the Clinical Operations team and partner with them to optimize feasibility, execution quality, enrollment strategies, and study delivery.
  • Ensure study designs appropriately balance scientific rigor, operational feasibility, project timelines, and resource requirements.
  • Participate in governance and risk mitigation activities for ongoing studies.
  • Support study execution through interpretation of emerging data and resolution of scientific issues.

What You'll Bring:

  • Advanced scientific or clinical degree (MD, PharmD, PhD, DNP, or equivalent).
  • Minimum 10 years of experience in clinical research, clinical development, medical affairs, or evidence generation.
  • Experience leading development and execution of clinical studies and evidence-generation programs.
  • Experience working within regulated healthcare environments.
  • Strong understanding of GCP, global regulatory expectations, and evidence-generation requirements.
  • Experience generating evidence across multiple evidence domains, including clinical outcomes, safety, workflow efficiency, human factors, usability, implementation science, real-world evidence, and health economic outcomes.
  • Builds trusted partnerships across Medical Affairs, Clinical Operations, Regulatory Affairs, R&D, HEOR, Commercial, and Quality.
  • Aligns diverse stakeholders around a common research vision.
  • Applies deep understanding of clinical research methodology to complex scientific and business questions.
  • Designs innovative evidence-generation approaches across pharmaceuticals, devices, and healthcare technologies.
  • Adapts rapidly to evolving portfolio priorities.
  • Effectively operates in ambiguity and changing business environments.
  • Demonstrates an entrepreneurial mindset.
  • Comfortable building new capabilities and processes.
  • Bias toward action and execution.
  • Challenges traditional approaches to accelerate learning and impact.
  • Balances innovation with scientific rigor.
  • Willingness to travel approximately 25% of the time.
  • Strong business acumen and impeccable integrity.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $224,000 - $308,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses, commission, and/or long-term incentive. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.
US Benefits at Baxter (except for Puerto Rico)
This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter
Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
Know Your Rights: Workplace Discrimination is Illegal
Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.
Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.
Originally posted on Himalayas

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