Emerald Clinical
Clinical Project Manager (Europe) - Talent Pipeline Opportunity
How your CV stacks up
Upload your CV to see how well it fits this job role
?%
Who We Are
Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases, offering Phase I-IV and real-world studies.
With over 25 years of experience and a world-renowned focus in renal research, Emerald Clinical has helped drive medical breakthroughs through deep scientific insight, flawless execution, and an unwavering commitment to quality.
Global Expertise. Local Insight. Real Impact.
Emerald Clinical is where science, speed, and strategy come together to transform healthcare. For over 25 years, we have led the way in clinical research, combining global reach with deep Asia-Pacific expertise and unparalleled local insight to deliver smarter trials and stronger outcomes.
Our 800+ employees that span across Asia-Pacific, Europe, and the Americas are embedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward.
About The Role
As Emerald Clinical Trials continues to expand across Europe, we are building a pipeline of experienced Clinical Project Managers to support future growth and upcoming study awards.
This is a pipelining opportunity. While this position may not represent an immediate opening, we are proactively identifying exceptional talent for anticipated projects. Candidates who apply may experience a delay in hiring updates while studies progress through award and start-up phases.
This is a home-based role within Europe, providing the opportunity to lead global and regional clinical trials across a range of therapeutic areas, with particular interest in candidates who bring experience within renal, oncology, cardiometabolic & autoimmune diseases.
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Your Responsibilities
- Provide leadership and oversight for assigned clinical projects from start-up through close-out.
- Act as the primary point of contact for sponsors, vendors, and internal stakeholders.
- Develop and maintain study timelines, budgets, forecasts, and project plans.
- Lead study teams to ensure delivery against quality, budget, and timeline expectations.
- Identify risks proactively and implement appropriate mitigation strategies.
- Oversee site activation, enrolment performance, monitoring activities, and study execution.
- Ensure compliance with ICH-GCP, applicable regulatory requirements, and company SOPs.
- Manage project finances and vendor performance.
- Support proposal development, business development activities, and bid defense meetings.
- Mentor and support Clinical Trial Managers, CRAs, and other project team members.
About You
- Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or related discipline.
- Approximately 7+ years of clinical research experience.
- Minimum 2 years of Project Management experience within a CRO environment.
- Previous experience managing global or regional studies.
- Strong client management and stakeholder engagement skills.
- Proven experience with project budgets and financial oversight.
- Excellent working knowledge of ICH-GCP and European regulatory requirements.
- Experience in renal/nephrology clinical trials is highly preferred.
- Experience across Phase I-IV clinical trials is advantageous.
Why Join Us?
Get help with your application
Your very own career expert that helps elevate your application to the next level.
At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first - both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide.
Here’s What Makes Us Stand Out
- Purpose-Driven Work: You’ll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.
- Global Reach, Local Expertise: Our teams connect with local communities, building trust and meaningful engagement for every trial.
- Collaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges.
What We Offer
- Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience.
- Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role.
- Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role.
- Employee Wellbeing: Participate in programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events.
- Global Opportunities: Be part of a company with international reach, offering you exposure to diverse projects and clients.
Interested? Apply now and help us achieve our mission to improve the health of millions worldwide.
We are an equal-opportunity employer and encourage applications from all qualified candidates.
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Skills