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- 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 and clinical study oversight experience.
- 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 hiring a Project Manager to work on global clinical studies and perform global trial management for a large global program. 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 planning and 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 as global trial manager. You will be part of an innovative and global Biotechnology company, who 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 onboarding
- 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 designed to be competitive within each country and focused on well-being and work-life balance opportunities for you and your family.
- 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, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized 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: ICON
Contact Detail:
ICON 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, especially those who work at ICON or similar companies. A friendly chat can sometimes lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. Understand their mission and values, and think about how your experience aligns with their goals. This will help you stand out as a candidate who truly gets what they’re about.
✨Tip Number 3
Practice your answers to common interview questions, but keep it natural. Use the STAR method (Situation, Task, Action, Result) to structure your responses, especially when discussing your project management experience.
✨Tip Number 4
Don’t forget to follow up after your interview! A quick thank-you email can leave a lasting impression and shows your enthusiasm for the role. Plus, it’s a great way to reiterate your interest in joining the ICON team.
We think you need these skills to ace Global Trial Manager in Reading
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Global Trial Manager role. Highlight your experience in managing international clinical studies and any relevant project management skills that align with what we’re looking for.
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 background makes you a perfect fit for our team. Don’t forget to mention your experience with risk management and budget oversight!
Showcase Your Teamwork Skills: We love collaboration! In your application, emphasise your experience working in cross-functional teams. Share examples of how you’ve led or contributed to successful projects in a matrix environment.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the details about the role and our company culture there!
How to prepare for a job interview at ICON
✨Know Your Stuff
Make sure you brush up on your knowledge of global clinical studies and the specific requirements of the role. Familiarise yourself with ICON plc's mission and values, as well as their approach to clinical trial management. This will help you demonstrate your genuine interest in the company and the position.
✨Showcase Your Experience
Prepare to discuss your previous experience managing international commercial clinical studies. Be ready to provide specific examples of how you've successfully overseen study deliverables, budgets, and timelines. Highlight any experience you have with external vendors and cross-functional teams, as this is crucial for the role.
✨Risk Management is Key
Since the role involves risk assessments and mitigation activities, be prepared to talk about your approach to project risk management. Share examples of how you've identified and resolved issues in past projects, and how you ensured that studies were delivered on time and within budget.
✨Ask Thoughtful Questions
At the end of the interview, don’t forget to ask insightful questions about the team dynamics, the challenges they face in global trial management, and how success is measured in this role. This shows your enthusiasm and helps you gauge if the company culture aligns with your values.
