远程工作雷达

临床策略负责人

Clinical Strategy Lead

其他限定地区(需当地身份)日间重叠仅 1 小时,需熬夜配合
公司Convatec
薪资未公开
工作地点United Kingdom
地域资格限定地区(需当地身份)
时区要求日间重叠仅 1 小时,需熬夜配合
用工类型Full Time
发布时间2 天前
数据来源Himalayas
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注意地域限制:该职位明确限定在 United Kingdom 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。
作息提示:日间重叠仅 1 小时,需熬夜配合。

引领值得信赖的医疗解决方案,改善我们所触及的生活:Convatec 是一家全球性的医疗产品和技术公司,专注于慢性病管理的解决方案,在先进伤口护理、造口护理、控尿护理和输注护理领域处于领先地位。公司拥有约 10,000 名员工,我们的产品和服务覆盖近 100 个国家,由一份永恒关怀的承诺所凝聚。我们的解决方案提供多种益处,从预防感染和保护高风险皮肤,到改善患者结果和降低护理成本。Convatec 在 2023 年的收入超过 20 亿美元。该公司是富时 100 指数的成分股(伦敦证券交易所:CTEC)。如需了解更多关于 Convatec 的信息,请访问

寻找更好的方式正在改变客户的生活,也在改变我们员工的职业生涯——不断创造新的挑战和机遇。我们是一家永不停歇的公司。加入团队,你也不会停滞。我们成功的临床策略负责人将参与所有与临床和医学事务相关的方面,重点是先进伤口护理医疗器械的证据生成和战略制定。该职位内容多样,涵盖多项活动,例如设计和执行临床研究方案、规划证据生成策略、回顾性分析和市场产品支持、生成出版物,以及识别该领域的未满足需求。您将与临床运营、全球医学教育、关键意见领袖管理、法规、质量、营销与业务发展以及研发同事保持密切联系。您还将与相关产品的关键意见领袖和医疗保健提供者建立关系。

主要职责和任务

  • 作为我们先进伤口护理医学和临床事务团队的临床策略师,特别关注新兴的先进伤口护理技术
  • 在临床研究设计中发挥主导作用,包括监管审批、统计分析计划和预算
  • 与全球医学教育和关键意见领袖管理同事以及业务发展和营销团队密切合作,通过与关键意见领袖、医疗保健提供者和监管机构的互动,分析并识别我们领域中的未满足需求
  • 与临床运营同事紧密合作,将商业战略转化为可操作的临床研究方案和回顾性数据分析计划
  • 分析数据
查看英文原文

Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit

search for better is changing the lives of our customers. It’s changing the careers of our people too – creating new challenges and opportunities all the time. We’re a business that never stands still. Join the team and you won’t either.Our successful Clinical Strategy Lead will be involved in all aspects of Clinical & Medical Affairs that focus on evidence generation and strategy development for Advanced Wound Care medical devices. The role is varied and incorporates multiple activities, such as designing and executing clinical study protocols, planning of evidence generation strategies, retrospective analyses and in-market product support, generation of publications, and identification of unmet needs in the field. You will have close liaison with Clinical Operations, Global Education, Regulatory, Quality, Marketing & Business Development, and R&D colleagues. You will also build relationships with key opinion leaders and healthcare providers relevant to the product.
Key Duties and Responsibilities

  • Act as a clinical strategist for our Advanced Wound Care Medical and Clinical Affairs team, with a special focus on emerging Advanced Wound Care technologies
  • Play a lead role in clinical study design, including regulatory approvals, statistical analysis plan, and budget.
  • Close collaboration with Global Medical Education and Key Opinion Leader Management colleagues and Business Development and Marketing teams through interactions with key opinion leaders, healthcare providers, and regulatory bodies to analyze and identify unmet needs in our field
  • Work closely with the clinical operations colleagues to translate business strategies to actionable clinical study protocols and retrospective data generation plans
  • Analyze data output from clinical studies and other evidence generation activities and distill these into a cohesive “story” to be presented when needed.
  • Play a proactive role in putting together publications and evidence communication in close collaboration with the medical writing team.
  • Act as an educator and role model for colleagues outside of medical affairs.
  • Support all our general medical affairs activities, including, but not limited to new product development, evidence generation and review, risk management, and other activities as needed.
  • Act as a subject matter expert in the product line.

Travel Requirements
Up to 20% overnight travel may be required, some of which will be international.
About You
You will bring a breadth of knowledge and experience in medical and clinical affairs. Must have knowledge in the life sciences, medicine, or nursing. Experience in a medical device, pharmaceutical, or academic setting is a plus.
Besides your professional attributes, you work independently while being a great team player with the ability to pivot as needs arise. You thrive in a fast-paced dynamic environment. You utilize your good communication skills to work in close collaboration with cross-functional teams. You are pragmatic and operate with a sense of urgency to meet your deadlines. You enjoy a busy working day and can progress several tasks in parallel, thriving with evolving changes and various tasks. You have proven analytical and problem-solving skills that will help you develop and maintain competitive and patient-centric clinical projects. You understand the importance of good documentation practices and see the value in creating solid documentation. You have excellent written and verbal communication skills in English.
Qualification & Experience

  • Bachelor’s degree or higher degree in Medicine, Life Sciences, Allied Health, Pharmacy, or Nursing. Advanced degree (MD, PhD MSN, DNP) preferred.
  • Clinical background (MD, RN, DPM, DNP, or similar) required
  • Specialty knowledge in wound care preferred.
  • At least 3 years’ experience in the medical device or pharmaceutical industry in positions of increasing responsibility.
  • Strong understanding of clinical research, including literature reviews, protocol development, general study execution, and statistical analysis.
  • Experience in clinical study design in an industry or academic setting.
  • Understanding of the medical device industry: product development, pre-clinical, clinical, quality, marketing, and regulatory components.
  • Experience with regulatory requirements for clinical studies in the US and EU is highly desirable.
  • A proven ability to deliver results according to timelines in a dynamic environment.
  • Strong computer skills and high level of proficiency of Microsoft Office.
  • Works both as a team member and independently, engages and supports other members of the team and willingly accepts support when required. Is able to make decisions and accept accountability.
  • Willingly embraces change and the need to adapt to new circumstances. Takes an innovative approach while maintaining compliance.
  • Effective use of oral and written communication skills to influence, inform or guide others.
  • Ability to communicate fluently in English.

Final compensation will be determined based on a variety of factors, including (but not limited to) geographic location, experience, knowledge, skills, and abilities. We also offer a comprehensive benefits package, which includes a retirement savings plan with company match, time off to include: paid vacation, holidays, community service days, sick time, paid caregiver/parental leave and medical leave, and health benefits for individuals, families, and domestic partners, including medical, prescription drug, dental, and vision coverage, in accordance with the terms of the applicable plans.
Ready to join us?
At Convatec, we’re pioneering trusted medical solutions to improve the lives we touch. If you’re ready to make a real impact, apply today and help us bring our Forever Caring promise to life.
Beware of scams online or from individuals claiming to represent Convatec
A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.
If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at .
Equal opportunities
Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
Notice to Agency and Search Firm Representatives
Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Already a Convatec employee?
If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!
About Convatec

Pioneering trusted medical solutions to improve the lives we touch:

Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With over 10,000 colleagues, we provide products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention, treatment for hard to heal wounds, at-risk skin and ulcerated tissue to supporting debilitating conditions, improved patient outcomes and reduced care costs. Convatec's revenues in 2025 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit:

Originally posted on Himalayas

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