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- Tasks: Lead global clinical studies, collaborating with teams to ensure successful execution and oversight.
- Company: IQVIA is a top global provider of clinical research services and healthcare intelligence.
- Benefits: Gain experience in a dynamic environment with opportunities for travel and professional growth.
- Why this job: Join a mission-driven team focused on improving patient outcomes through innovative medical treatments.
- Qualifications: 5+ years in clinical research, strong project leadership, and ability to manage complex studies.
- Other info: This role requires flexibility in schedule and international travel; UK visa sponsorship not available.
The predicted salary is between 43200 - 72000 £ per year.
The Global Clinical Lead/Study Lead – Country Operations – (SLCO) serves as the primary contact for the Country Operations Management (COM) team on a global study level, collaborating closely with the Clinical Project Lead (CPL) and other functional stakeholders. This role acts as the global representative for COM, facilitating communication between in-country teams and the global study team.
Key Responsibilities
• Collaborate with global and country teams to define the appropriate country footprint for the study and consolidate information to support internal governance approvals.
• Lead Key External Expert (KEE) outreach activities in partnership with Alexion Global Feasibility & Site Intelligence (GFSI) to evaluate study design suitability and identify opportunities for protocol improvement.
• Coordinate detailed site feasibility assessments with GFSI and work with country teams to finalize the proposed breakdown of countries, sites, and patients for endorsement by the Global Program Team (GPT).
• Oversee site start-up (SSU) activities performed by country teams and/or CRO partners.
• Contribute to the development and execution of patient recruitment, retention, and engagement strategies, including insights from patient activities.
• Maintain oversight of study deliverables and site monitoring throughout the trial lifecycle, ensuring inspection readiness at all times.
• Address risks or issues related to site management and monitoring in collaboration with global and country-level stakeholders.
Qualifications, Expertise and Skillset
• 5+ years of clinical research experience in Biopharma or CRO
• Experience of managing multiple studies including extensive experience in the management and oversight of CROs
• Experience of ultra-rare disease clinical research is beneficial
• Demonstrated project leadership skills
• Extensive clinical trial experience across a range of complex disease areas
• Demonstrated capability of effective monitoring oversight
• Ability to operate effectively in a highly matrixed team environment
• Ability to work autonomously and within a team structure and able to demonstrate initiative
• Solid knowledge of clinical development processes with strong emphasis on monitoring
• Track record of establishing effective relationships with investigator sites
• Ability to lead, troubleshoot and influence for quality and delivery
• A track record of ensuring GCP compliance and successful risk management of complex clinical studies is expected
• Demonstrates flexibility in schedule and ability to travel as required internationally and domestically
This role is not eligible for UK visa sponsorship
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
Global Clinical Lead - Sponsor Dedicated employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Clinical Lead - Sponsor Dedicated
✨Tip Number 1
Make sure to familiarize yourself with the latest trends and developments in clinical research, especially in the biopharma sector. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in a rapidly evolving field.
✨Tip Number 2
Network with professionals who are currently working in similar roles or companies. Attend industry conferences or webinars to connect with potential colleagues and learn more about the specific challenges and opportunities in global clinical operations.
✨Tip Number 3
Prepare to discuss your experience with managing multiple studies and CRO oversight in detail. Be ready to share specific examples of how you've successfully navigated complex clinical trials and maintained GCP compliance.
✨Tip Number 4
Highlight your ability to work autonomously as well as part of a team. Provide examples of how you've demonstrated initiative in previous roles, particularly in challenging situations that required effective problem-solving and leadership.
We think you need these skills to ace Global Clinical Lead - Sponsor Dedicated
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly read the job description for the Global Clinical Lead position. Understand the key responsibilities and qualifications required, and think about how your experience aligns with these.
Tailor Your CV: Customize your CV to highlight relevant clinical research experience, particularly in managing multiple studies and CRO oversight. Emphasize any experience you have with ultra-rare diseases and project leadership.
Craft a Compelling Cover Letter: Write a cover letter that showcases your understanding of the role and your passion for clinical research. Mention specific experiences that demonstrate your ability to lead and manage complex studies effectively.
Highlight Key Skills: In your application, make sure to emphasize your skills in monitoring oversight, relationship building with investigator sites, and your track record in ensuring GCP compliance. These are crucial for the role.
How to prepare for a job interview at IQVIA
✨Understand the Role and Responsibilities
Make sure you have a clear understanding of the Global Clinical Lead position and its key responsibilities. Familiarize yourself with the collaboration between the Country Operations Management team and the Clinical Project Lead, as well as the importance of effective communication across teams.
✨Showcase Your Experience
Prepare to discuss your clinical research experience, especially in managing multiple studies and overseeing CROs. Highlight any specific experiences related to ultra-rare disease clinical research, as this could set you apart from other candidates.
✨Demonstrate Leadership Skills
Be ready to provide examples of how you've demonstrated project leadership in previous roles. Discuss situations where you led teams, influenced outcomes, or managed risks effectively, showcasing your ability to operate in a matrixed environment.
✨Prepare for Behavioral Questions
Expect questions that assess your problem-solving abilities and flexibility. Prepare scenarios where you had to troubleshoot issues or adapt to changing circumstances, particularly in relation to site management and monitoring during clinical trials.
