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Project Manager, eCOA

Role overview

Qualifications

  • Bachelor’s degree or equivalent combination of education and relevant experience
  • 1–4 years of project management experience, preferably within pharmaceuticals or healthcare environments
  • Understanding of the drug development process and clinical trial lifecycle
  • Project Management certification or willingness to pursue professional development in project management

Responsibilities

  • 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
  • Identify potential risks and issues, implement mitigation strategies, and escalate concerns when appropriate

Key facts

Hard skills

Other skills

  • Organizational Skills
  • Communication
  • Problem Solving
  • Microsoft Office
  • Detail Oriented
  • Time Management

About the company

Clario logo

Clario

Contract Research Organizations (CRO)

Clario is a leading healthcare research and technology company that generates high quality clinical evidence for our pharmaceutical, biotech, and medical device partners. We offer comprehensive evidence generation solutions that combine eCOA, cardiac safety, medical imaging, precision motion, and respiratory endpoints. Since our founding more than 50 years ago, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported clinical trials over 26,000 times in more than 100 countries. Our global team of science, technology, and operational experts have supported over 60% of all FDA drug approvals since 2019. For more information, visit Clario.com

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size1001 - 5000

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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 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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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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