区域临床试验经理
Regional Clinical Trial Manager
区域临床试验经理 - 台湾 - 远程办公
ICON 是一家全球医疗智能和临床研究组织，致力于更快地将新药和治疗方法带给患者。
作为一家以价值观为导向的组织，诚信、协作、敏捷和包容是我们工作和与彼此、客户、患者及供应商互动的核心。
在 ICON 担任临床试验经理，您将负责管理临床试验运营活动，支持您的团队和相关方在我们的临床项目中实现高质量成果。
您将负责：
您将管理日常临床试验管理工作，支持团队实现高质量成果。
主要职责包括：
- 计划和管理临床试验的所有方面，确保符合时间表、预算和质量标准。
- 与跨职能团队合作，建立并实施临床试验方案和流程。
- 与试验研究人员和相关方建立并维护良好的关系。
- 确保所有试验符合当地、国家和国际法规及伦理准则。
- 解决问题并就试验设计、供应商选择和风险管理做出关键决策。
您的背景：
您将具备扎实的临床试验管理经验，能够管理优先级冲突并培养团队。
所需资格和经验：
- 医学、科学或同等教育与经验组合的大学学位
- 在研究中展示推动临床交付成果的能力
- 在指定治疗领域具备专业知识
- 有监查经验者优先
- 根据需要愿意出差（约25%）
在 ICON 就职的前提是您必须拥有在该职位所在国家合法工作的权利。
奖励与福利
ICON 提供具有竞争力且全面的总薪酬包，旨在支持您的健康、福祉和职业发展。
福利可能包括：
- 具有竞争力的基本薪资和绩效相关激励
- 健康和福祉计划，包括适用的医疗、牙科和视力保险
- 退休和养老金计划
- 寿命保障和残疾保险
- 员工援助计划和福祉资源
- 通过结构化培训和职业发展路径提供的学习和发展机会
福利可能因地区而异
查看英文原文
Regional Clinical Trial Manager- Taiwan - Remote
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.
What You Will Do:
You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes.
Key responsibilities include:
- Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
- Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
- Build and manage strong relationships with trial investigators and stakeholders.
- Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
- Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.
Your Profile:
You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
- University degree in medicine, science, or equivalent combination of education & experience
- Demonstrated ability to drive the clinical deliverables of a study
- Subject matter expertise in the designated therapeutic area
- Prior monitoring experience is preferred
- Willingness to travel as required (approximately 25%)
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
Originally posted on Himalayas