Global Trial Manager in Reading
Global Trial Manager

Global Trial Manager in Reading

Reading Full-Time 36000 - 60000 £ / year (est.) Home office possible
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At a Glance

  • Tasks: Lead global clinical studies and manage cross-functional teams to ensure successful project delivery.
  • Company: Join ICON plc, a leading healthcare intelligence and clinical research organisation.
  • Benefits: Enjoy competitive salary, health insurance, flexible benefits, and a supportive work-life balance.
  • Why this job: Make a real impact in the biotech field while working from home in the UK.
  • Qualifications: 7 years in life sciences with strong project management experience in clinical trials.
  • Other info: Inclusive culture focused on innovation and career growth opportunities.

The predicted salary is between 36000 - 60000 £ per year.

ICON plc is a world-leading healthcare intelligence and clinical research organization. We are proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are hiring a Project Manager to work on global clinical studies with significant project management experience within clinical global trials management. The role is homebased in the UK.

Do you have experience of managing international commercial clinical studies within a CRO or pharma setting? Can you demonstrate strong project planning and study management skills to meet study deliverables and budget? Do you have solid full service (FSP) study oversight experience?

This is a great opportunity to join our global clinical trial management team. You will be part of an innovative and global Biotechnology company, who pride themselves to be one of the world's leading independent biotechnology companies. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society today.

The role:

  • Planning and management of clinical studies conducted by global development team through the leadership of the cross-functional clinical study team
  • Contributing to study-level risk assessments
  • Leading and continually reviewing risk mitigation activities to ensure study delivery to plan
  • Identifying and resolving issues at a global level
  • Collaborating with Regional Clinical Trial Manager to ensure country level study delivery aligned with global delivery plans
  • Overseeing global insourcing/outsourcing partner deliverables to the required standards
  • Managing study-level budget and timelines
  • Leading global study-level documentation and required tool and systems set-up
  • Leading development and implementation of global Drug Supply Plan

What is required:

  • BA/BS/BSc or RN
  • Ideally 7 years work experience in life sciences or medically related field, including 4 years ideally of bio-pharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
  • Previous clinical study management/clinical project management as a study manager/clinical project manager
  • Experience in overseeing external clinical research vendors (CROs, central labs, imaging vendors, etc.) highly preferred
  • Project management experience including oversight of study deliverables, budgets, and timelines
  • Experience collaborating and leading cross-functional teams (team/matrix environment)
  • Knowledge of project risk management assessment and mitigation approaches

What is offered:

  • Solid structured on-boarding
  • Full-time and permanent contract of employment with us seconded to one single sponsor
  • Homebased in the UK/England
  • Salary according to level of skills and experience

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Global Trial Manager in Reading employer: IRE

ICON plc is an exceptional employer, offering a dynamic and inclusive work environment that prioritises innovation and excellence in the healthcare sector. As a Global Trial Manager, you will benefit from a comprehensive onboarding process, competitive salary, and a range of health and wellness benefits designed to support your work-life balance. With a strong focus on employee growth and development, ICON provides ample opportunities for career advancement within a leading biotechnology company dedicated to addressing unmet medical needs globally.
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Contact Detail:

IRE Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Global Trial Manager in Reading

✨Tip Number 1

Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. You never know who might have the inside scoop on job openings or can refer you directly.

✨Tip Number 2

Prepare for interviews by researching the company and its culture. Understand their mission and values, especially how they align with your own. This will help you tailor your responses and show that you're genuinely interested in being part of their team.

✨Tip Number 3

Practice your pitch! Be ready to explain your experience and how it relates to the role of Global Trial Manager. Highlight your project management skills and any relevant clinical trial experience to make a strong impression.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect with us directly.

We think you need these skills to ace Global Trial Manager in Reading

Project Management
Clinical Trial Management
Study Planning
Budget Management
Risk Assessment
Cross-Functional Team Leadership
Vendor Oversight
Clinical Research Experience
Problem-Solving Skills
Communication Skills
Time Management
Collaboration Skills
Adaptability
Attention to Detail

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Global Trial Manager role. Highlight your project management experience in clinical trials and any relevant skills that match the job description. We want to see how your background aligns with our needs!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your experience makes you a great fit for our team. Keep it engaging and personal – we love to see your personality come through.

Showcase Your Achievements: When detailing your experience, focus on specific achievements rather than just duties. Use metrics where possible to demonstrate your impact in previous roles. We’re keen to see how you’ve contributed to successful study outcomes!

Apply Through Our Website: We encourage you to apply directly through our careers site. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the info you need about the role and our company culture there!

How to prepare for a job interview at IRE

✨Know Your Stuff

Make sure you brush up on your knowledge of global clinical trials and project management. Familiarise yourself with the specific methodologies and regulations that apply to the role, as well as any recent developments in the biotech field. This will help you answer questions confidently and show that you're genuinely interested in the position.

✨Showcase Your Experience

Prepare to discuss your previous experience managing international clinical studies. Be ready to provide specific examples of how you've handled project planning, risk assessments, and budget management. Use the STAR method (Situation, Task, Action, Result) to structure your responses and highlight your achievements.

✨Ask Insightful Questions

Interviews are a two-way street, so come prepared with thoughtful questions about the company's approach to clinical trials and their team dynamics. This not only shows your interest but also helps you gauge if the company culture aligns with your values and work style.

✨Demonstrate Team Leadership Skills

Since the role involves leading cross-functional teams, be prepared to discuss your leadership style and how you motivate and manage diverse groups. Share examples of how you've successfully collaborated with different stakeholders to achieve study deliverables, and emphasise your ability to resolve conflicts and drive results.

Global Trial Manager in Reading
IRE
Location: Reading

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