Emerald Clinical Trials

Clinical Project Manager (Europe) - Talent Pipeline Opportunity

Emerald Clinical Trials Tirana, Central Albania, Albania

Biotechnology Research · 501-1,000 employees

8 h ago
Remote project-manager Senior (5-10 yrs) Full-time Portugal
Log in to apply, save this posting, or score it against your profile with AI.

About the role

The Clinical Project Manager will provide leadership and oversight for clinical projects from start-up through close-out, acting as the primary point of contact for stakeholders. They are responsible for managing study timelines, budgets, and project plans while ensuring compliance with regulatory requirements and company SOPs.

What they look for

Clinical project management Stakeholder engagement Budget management ICH-GCP compliance Risk mitigation Site activation Clinical trial oversight Vendor management Proposal development Business development Mentoring Regulatory compliance Renal research Oncology Cardiometabolic diseases Autoimmune diseases

Requirements

Candidates must hold a Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or a related discipline. The role requires approximately 7+ years of clinical research experience, including at least 2 years of project management experience within a CRO environment.

Benefits

Competitive compensation Remote working arrangements Career growth opportunities Employee wellbeing programs Recognition programs Team-building events

Full description

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.

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?

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

We understand that great work happens when people feel valued and supported. That’s why we provide:

· 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.

Similar roles