Project Manager, eCOA at Clario

Shanghai, Shanghai, China -

Full Time

Start Date

Immediate

Expiry Date

30 Sep, 26

Salary

0.0

Posted On

02 Jul, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Management, eCOA, Clinical Research, Budget Management, Risk Mitigation, Stakeholder Coordination, Regulatory Compliance, Microsoft Office, Customer Service, Problem Solving, Timeline Management, Drug Development Lifecycle

Industry

Biotechnology Research

Description

At Clario, a part of Thermo Fisher Scientific, we are dedicated to transforming lives by unlocking better evidence in clinical research. As a Project Manager, eCOA, you will play a critical role in delivering high-quality, compliant, and client-focused study solutions. You will manage end-to-end project execution, ensuring timelines, budgets, and customer expectations are met while fostering strong collaboration across global teams and clients. What We Offer Competitive compensation Flexible working arrangements supporting work-life balance Opportunities for professional development and career growth Collaborative, global team environment What You’ll Be Doing Lead the planning, setup, monitoring, and closeout phases of eCOA study management across multiple client projects Gather and translate customer requirements into actionable deliverables for internal teams Develop and maintain study documentation, reports, and data archives in compliance with regulatory standards Manage study timelines, budgets, forecasting, scope changes, and invoice reconciliation to ensure financial accuracy Identify and mitigate study risks, proactively escalating issues and driving resolution Coordinate internal and external stakeholders, fostering effective communication and collaboration to meet contractual obligations Oversee equipment distribution and tracking to ensure timely study execution Apply structured problem-solving approaches to resolve client issues and maintain issue tracking documentation Present study services at investigator meetings and support client discussions alongside Business Development and Operations teams Support onboarding and training of new Project Management team members as needed What We Look For Bachelor’s degree or equivalent practical experience in project management or a related field 1–4 years of project management experience within the pharmaceutical or related industry Understanding of the drug development lifecycle and clinical research processes Proven ability to manage multiple priorities, timelines, and stakeholders effectively Strong organizational, interpersonal, and time management skills Excellent verbal and written communication skills in English Proficiency with Microsoft Office tools (e.g., Excel, PowerPoint, Word) Detail-oriented with a strong focus on responsiveness and customer service Ability to identify risks and drive proactive problem resolution Valid passport and willingness to travel up to 20% as required At Clario, a part of Thermo Fisher Scientific, a 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.

Responsibilities

Lead the end-to-end execution of eCOA study management, including planning, monitoring, and closeout phases. Manage project timelines, budgets, and stakeholder communications to ensure high-quality, compliant clinical research solutions.