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- Tasks: Lead global clinical studies and manage cross-functional teams to ensure successful project delivery.
- Company: Join ICON plc, a top-tier biotechnology company focused on innovative healthcare solutions.
- Benefits: Enjoy remote work flexibility, competitive salary, and comprehensive employee benefits.
- Why this job: Be part of a mission-driven team that impacts lives through cutting-edge clinical research.
- Qualifications: 7 years in life sciences with 4 years in clinical project management required.
- Other info: Inclusive workplace culture committed to professional development and employee wellbeing.
The predicted salary is between 36000 - 60000 £ per year.
We are hiring a Project Manager to start asap and perform global trial management for a large and well-established 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 full service/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 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 review 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
Why Join?
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best-in-class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
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.
Global Trial Manager employer: ICON Strategic Solutions
Contact Detail:
ICON Strategic Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Trial Manager
✨Tip Number 1
Network with professionals in the clinical research field, especially those who have experience in global trial management. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends in clinical studies.
✨Tip Number 2
Familiarise yourself with the specific challenges and regulations of managing international clinical trials. Understanding the nuances of different countries' regulatory environments can set you apart from other candidates.
✨Tip Number 3
Demonstrate your project management skills by discussing relevant experiences where you successfully managed budgets and timelines. Be prepared to share specific examples during interviews that highlight your ability to lead cross-functional teams.
✨Tip Number 4
Stay updated on the latest advancements in biotechnology and clinical research methodologies. Showing your passion for the field and your commitment to continuous learning can make a strong impression on hiring managers.
We think you need these skills to ace Global Trial Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in managing international clinical studies, particularly within a CRO or pharmaceutical setting. Emphasise your project management skills and any specific achievements that align with the job requirements.
Craft a Compelling Cover Letter: Write a cover letter that clearly outlines your motivation for applying to this role. Discuss your experience in clinical trial management and how it relates to the responsibilities mentioned in the job description. Be sure to convey your passion for contributing to innovative biotechnology solutions.
Highlight Relevant Skills: In your application, specifically mention your experience with risk management, budget oversight, and cross-functional team leadership. Use examples from your past roles to demonstrate how you have successfully navigated challenges in clinical study management.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in project management roles.
How to prepare for a job interview at ICON Strategic Solutions
✨Showcase Your Experience
Make sure to highlight your experience in managing international clinical studies. Be prepared to discuss specific projects you've worked on, the challenges you faced, and how you overcame them.
✨Demonstrate Planning Skills
Since the role requires strong planning and management skills, come equipped with examples of how you've successfully managed budgets and timelines in previous roles. Use metrics to quantify your success.
✨Understand Risk Management
Familiarise yourself with project risk management assessment and mitigation approaches. Be ready to discuss how you've identified and resolved issues in past projects, particularly at a global level.
✨Collaborate Effectively
The role involves working with cross-functional teams, so be prepared to talk about your experience in leading and collaborating with diverse teams. Share examples that demonstrate your ability to align team efforts with global delivery plans.
