全球研究经理 - 英国（居家办公）- 6 个月合同制 - FSP
Global Study Manager - UK (Home-based) - 6 Month FTC - FSP
当我们的价值观一致时，我们能够实现的没有界限。
在Parexel，我们都有相同的目标——改善全球健康。从临床试验到监管、咨询和市场准入，我们提供的每一个临床开发解决方案都建立在一个特别的基础上——对我们所做事情的深刻信念。
无论我们在Parexel做什么，每个人都在为最终能惠及患者的疗法开发做出贡献。我们认真对待工作，带着同理心去做，并致力于带来改变。
关于Parexel
Parexel是领先的全球临床开发合作伙伴，为生命科学行业提供以洞察为导向的临床和咨询服务。全球拥有22,000多名员工，我们与生物制药公司和研究机构合作，设计并开展以患者为中心的临床试验，扩大参与范围，使研究成为任何地方任何人的治疗选择。
我们专注、敏捷且有共同目标地工作——迅速响应患者需求，加速新疗法的交付。我们鼓励大胆思考，快速适应变化，并持续提高临床研究的速度和质量。我们正在扩大团队，寻找有才华的人士来推动行业领先的创新，With Heart®。
职位介绍
我们正在寻找有经验的全球研究经理（GSM），具有丰富的肿瘤学试验经验，以远程方式在英国工作，合同期为6个月的固定期限合同。作为GSM，您将负责从启动到执行再到研究结束的全球研究活动。
全球研究运营经理负责所分配研究的研究管理方面，包括供应商和预算管理。
您将支持推进新治疗方法的临床研究活动，并与全球跨职能团队合作。
您将加入一个快节奏、注重成长的环境，通过设立、执行和交付所分配的试验来产生有意义的影响，并通过准确的规划和高效执行试验，为赞助商的管线做出贡献，为参与的受试者和研究中心带来速度和价值。
在多元化的团队和持续的学习机会中，全球研究经理可以探索职业发展路径，并拓展临床研究方面的技能。
这些职位将是完全远程在家办公。
主要职责
- 全球研究层面的实施
查看英文原文
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
About Parexel
Parexel is a leading global clinical development partner delivering insights‑driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient‑focused clinical trials that broaden access and make research a care option for anyone, anywhere.
We work with focus, agility, and shared purpose – moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry‑leading innovation, With Heart®.
About the Role
We are seeking experienced Global Study Managers (GSM) with strong oncology trials experience to join our team in a remote capacity in the UK on a 6-month fixed term contract basis. As a GSM you will be responsible for global study activities from start up through conduct and study close.
The Global Study Operations Manager has responsibility for study management aspects of assigned studies, including vendor and budget management.
You will support clinical research activities that advance new treatments for patients and collaborate with global cross‑functional teams.
You’ll join a fast‑paced, growth‑oriented environment focused on making a meaningful impact through the set-up, execution and delivery of assigned trials and contribute to delivery of the sponsors pipeline through accurate planning and efficient execution of trials that bring speed and value to participating subjects and sites.
With diverse teams and continuous learning opportunities, the Global Study Manager can explore career paths and expand skills across clinical research.
These will be fully remote home-based positions.
Key Responsibilities
- Global Study level implementation of Start-up and Site Activation Plans
- Responsible for global/regional study level Recruitment Strategy
- Responsible to support the development of global study level plans
- Communication with both global and local teams, internal stakeholders and CRO partner as applicable and as listed above to ensure efficient and timely study delivery of the agreed plans
- Responsible for study vendor management and oversight including follow up and coordination of vendor deliverables
Candidate Profile
You’ll thrive in this role if you bring:
- Extensive experience in clinical trial project management across international trials
- Global experience working in clinical research, healthcare, or a regulated environment
- The ability to collaborate across teams and communicate clearly
- A patient‑focused mindset and strong attention to detail
- The ability to work independently and exercise your own judgement
Required Qualifications
- M.S/M.A/Ph.D or B.A/B.S/nursing degree is essential. (Master’s is preferred)
- Minimum of 5 years’ relevant experience in clinical trial management
- Excellent leadership, communication, and organizational skills. Able to multi-task under limited direction and on own initiative.
- Strong communication, organization, and problem‑solving skills
- Fluency in English, both written and spoken
- Prior and demonstrable experience working at a senior level within Study start up is preferred.
If this job doesn’t sound like the next step in your career, but perhaps you know of someone who’d be a perfect fit, send them the link to apply!
We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.
Originally posted on Himalayas