At a Glance
- Tasks: Lead complex clinical studies from start to finish, ensuring everything runs smoothly.
- Company: Join a dynamic team in a leading global healthcare company.
- Benefits: Competitive daily rate, remote work flexibility, and valuable industry experience.
- Other info: Temporary role with potential for growth in a fast-paced environment.
- Why this job: Make a real impact in healthcare by driving successful study outcomes.
- Qualifications: Proven experience as a Study Manager and strong leadership skills.
The predicted salary is between 50000 - 61500 € per year.
Type: Temporary
Duration: 7 months approx. (until end of 2026)
Location: Remote (client based in London)
Rate: circa. £500-615 per day (via Umbrella, INSIDE IR35)
We are seeking multiple experienced Study Managers to oversee the delivery of complex studies from initiation through to completion. This is a key role requiring strong leadership, operational oversight, and the ability to drive high-quality study execution in a fast-paced environment. This role is ideal for candidates with solid Study Management experience who can confidently take ownership of study delivery and drive successful outcomes.
Key Responsibilities- Manage end-to-end study delivery, ensuring milestones, timelines, and budgets are met
- Act as the primary point of accountability for study execution and performance
- Coordinate cross-functional teams (clinical, data, regulatory, vendors) to ensure alignment
- Oversee study planning, risk management, and issue resolution
- Ensure compliance with regulatory requirements, SOPs, and quality standards
- Manage vendor relationships and external partners to ensure effective delivery
- Proven experience as a Study Manager (essential)
Global Clinical Study Manager employer: Lorien
As a Global Clinical Study Manager with our client, you will be part of a dynamic and innovative team that values leadership and operational excellence. The remote working arrangement allows for flexibility while collaborating with top-tier professionals in the industry, fostering a culture of growth and continuous improvement. With competitive rates and a focus on high-quality study execution, this role offers a unique opportunity to make a significant impact in the field of clinical research.
StudySmarter Expert Advice🤫
We think this is how you could land Global Clinical Study Manager
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your study management skills. Be ready to discuss specific projects you've managed, how you handled challenges, and your approach to ensuring compliance and quality standards.
✨Tip Number 3
Showcase your leadership abilities! During interviews, highlight instances where you've successfully coordinated cross-functional teams and driven high-quality outcomes. This is key for a Global Clinical Study Manager role.
✨Tip Number 4
Don't forget to apply through our website! We’ve got some fantastic opportunities waiting for you, and applying directly can give you an edge. Plus, it’s super easy to keep track of your applications!
We think you need these skills to ace Global Clinical Study Manager
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Global Clinical Study Manager role. Highlight your relevant experience in study management and any leadership roles you've held. We want to see how you can take ownership of study delivery!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Share specific examples of how you've successfully managed studies in the past, and don’t forget to mention your ability to drive high-quality outcomes.
Showcase Your Teamwork Skills:Since this role involves coordinating cross-functional teams, make sure to highlight your teamwork skills. We love candidates who can effectively collaborate with clinical, data, and regulatory teams to ensure everything runs smoothly.
Apply Through Our Website:We encourage you to apply through our website for a seamless application process. It’s the best way for us to receive your application and get to know you better. Don’t miss out on this opportunity!
How to prepare for a job interview at Lorien
✨Know Your Studies Inside Out
Before the interview, make sure you’re well-versed in the specifics of clinical study management. Brush up on your past experiences and be ready to discuss how you've successfully managed studies from initiation to completion, including any challenges you faced and how you overcame them.
✨Showcase Your Leadership Skills
This role requires strong leadership, so be prepared to share examples of how you've led cross-functional teams in the past. Highlight your ability to coordinate with clinical, data, and regulatory teams, and demonstrate how you’ve driven high-quality outcomes in a fast-paced environment.
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations related to study management. Think about how you would handle risk management, issue resolution, and vendor relationships. Practising these scenarios can help you articulate your thought process clearly during the interview.
✨Understand Regulatory Compliance
Since compliance is crucial in clinical studies, brush up on relevant regulations and quality standards. Be prepared to discuss how you ensure adherence to these requirements in your previous roles, as this will show your potential employer that you take compliance seriously.
