Manage end-to-end delivery of electronic Clinical Outcome Assessment studies for clinical trials. Responsibilities include planning, setup, execution, monitoring, closeout, client communication, requirements gathering, documentation, budget and timeline tracking, risk mitigation, cross-functional coordination, and quality compliance. The role also supports client presentations, team onboarding, training, and knowledge sharing while ensuring accurate delivery of digital patient data collection solutions.
Join Clario, part of Thermo Fisher Scientific, as a Project Manager eCOA in the United Kingdom and play a key role in delivering electronic Clinical Outcome Assessment (eCOA) solutions that support clinical trials worldwide. In this role, you will coordinate the successful delivery of digital patient data collection solutions, ensuring projects are completed on time, within budget, and to the highest quality standards. Your work will help sponsors collect accurate, real-time patient data, improve compliance, and accelerate the development of life-changing therapies.
What we offer
- Competitive compensation
- Attractive benefits focused on security, flexibility, support, and well-being
- Engaging employee programs and development opportunities
- Remote working and home office allowance
What you'll be doing
- Manage all phases of study delivery, including planning, setup, execution, monitoring, and closeout
- Act as the primary point of contact for assigned studies, ensuring clear communication with clients and internal teams
- Gather and document customer requirements and translate them into actionable project deliverables
- Develop and maintain study documentation, monitor project milestones, and oversee study-related activities
- Track project timelines, budgets, forecasts, invoicing, and scope changes to ensure successful delivery
- Identify potential risks and issues, implement mitigation strategies, and escalate concerns when appropriate
- Coordinate cross-functional teams to ensure collaboration and alignment throughout the project lifecycle
- Present study services and project updates during client meetings and internal discussions
- Support onboarding, knowledge sharing, and training of new team members
- Maintain compliance with applicable processes, training requirements, quality standards, and documentation procedures
What we look for
- Bachelor’s degree or equivalent combination of education and relevant experience
- 1–4 years of project management experience, preferably within pharmaceuticals, biotechnology, contract research, clinical research, or healthcare environments
- Understanding of the drug development process and clinical trial lifecycle
- Strong organizational, communication, stakeholder management, and problem-solving skills
- Ability to manage multiple priorities while maintaining a high level of accuracy and attention to detail
- Customer-focused mindset with the ability to build effective working relationships
- Proficiency with Microsoft Office applications
- Project Management certification or willingness to pursue professional development in project management
- Valid passport and willingness to travel up to 20% as business needs require
At Clario, part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.
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