Project Manager, eCOA

Clario; United Kingdom; Remote; GBP 42,000 - 64,000; Full time

Benefits offered by this job

Competitive compensation

Flexible benefits and well-being focus

Employee development programs

Remote work and home office allowance

Job summary

Clario, part of Thermo Fisher Scientific, is hiring a Project Manager eCOA in the United Kingdom to drive electronic Clinical Outcome Assessment solutions for global trials. You will coordinate digital patient data collection, ensuring on-time, on-budget delivery with high quality to support sponsors and accelerate therapies.

You will lead end-to-end study delivery, liaise with clients and internal teams, document requirements, manage budgets and timelines, and ensure compliance with quality

Qualifications

• Bachelor’s degree or equivalent combination of education and experience.
• 1–4 years of project management experience in pharma/biotech/clinical research or healthcare.
• Understanding of drug development and clinical trial lifecycle.
• Strong organizational, communication, stakeholder management, and problem-solving skills.
• Ability to manage multiple priorities with high accuracy.
• Customer-focused mindset and relationship-building ability.
• Proficiency with Microsoft Office applications.
• PM certification or willingness to pursue development.
• Valid passport and willingness to travel up to 20%.

Responsibilities

• Manage all phases of study delivery: planning, setup, execution, monitoring, closeout.
• Act as primary contact for assigned studies with clients and internal teams.
• Gather and document customer requirements and translate into deliverables.
• Develop and maintain study documentation, monitor milestones and activities.
• Track timelines, budgets, forecasts, invoicing, and scope changes.
• Identify risks, implement mitigations, and escalate when needed.
• Coordinate cross-functional teams for alignment throughout the lifecycle.
• Present study services and updates during client meetings and internal discussions.
• Support onboarding, knowledge sharing and training of new team members.
• Maintain compliance with processes, training, quality standards, and documentation.

Skills

Organizational skills

Communication skills

Stakeholder management

Problem-solving

Education

Bachelor’s degree

Tools

Microsoft Office

Job description

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 elevate 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. Clario Privacy Policy Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.