eCOA Project Manage- Remote/North America (US, Canada, Mexico) & Argentina
PharmaCRO
Job description
eCOA Project Manage- Remote/North America (US, Canada, Mexico) & Argentina Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. • We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities eCOA Project Manager Remote - North America (United States, Canada, Mexico, Argentina) Are you an experienced project manager with a passion for clinical technology, digital health solutions, and improving the patient experience in clinical research? Do you thrive at the intersection of clinical operations, software implementation, vendor management, and stakeholder collaboration? We are seeking an eCOA Project Manager to join our growing Clinical Surveillance & Training (CST) organization. In this highly visible role, you will lead the end-to-end delivery of electronic Clinical Outcome Assessment (eCOA) solutions across global clinical trials, serving as the primary point of accountability for study-specific eCOA implementation and oversight. This is an exciting opportunity for a project management professional who enjoys driving complex technology-enabled clinical programs, collaborating with global stakeholders, managing multiple vendors, and ensuring high-quality electronic data collection solutions that support study endpoints, patient engagement, and data integrity. You will be joining a highly collaborative and supportive team known for its strong culture, long-tenured leadership, and commitment to helping one another succeed. WHAT YOU WILL DO As an eCOA Project Manager , you will oversee the planning, implementation, delivery, and ongoing management of eCOA solutions throughout the clinical trial lifecycle. You will act as the primary liaison between internal stakeholders, sponsors, and eCOA vendors to ensure systems are configured accurately, tested thoroughly, and delivered on schedule. eCOA Strategy & Study Delivery Lead eCOA activities from study startup through closeout. Manage study-specific eCOA project plans, timelines, milestones, and deliverables. Serve as the primary eCOA subject matter expert for assigned clinical studies. Ensure electronic assessments align with protocol requirements, study objectives, and regulatory expectations. Support global studies involving patient-reported outcomes, clinician-reported outcomes, and other electronic assessments. Drive implementation of lessons learned and continuous improvement best practices across programs. eCOA System Build & Oversight Oversee study-specific eCOA software design, configuration, and deployment. Manage eCOA system builds, including: Questionnaires and instruments Scales and assessments Visit schedules Device configurations Language requirements Study workflows Ensure systems are built, validated, and maintained with a high degree of accuracy. Review and approve vendor deliverables throughout the build lifecycle. Coordinate system updates, enhancements, and ongoing maintenance activities. User Acceptance Testing (UAT) Develop comprehensive User Acceptance Testing (UAT) strategies and test scripts. Lead and execute UAT activities to validate study functionality. Identify, document, and resolve testing issues in collaboration with vendors and stakeholders. Ensure all eCOA solutions meet quality expectations before deployment. Drive inspection-ready documentation and testing records. Vendor & Stakeholder Management Serve as the primary liaison between sponsors, internal teams, and eCOA vendors. Manage vendor timelines, deliverables, risks, and issue resolution. Build strong relationships with sponsors and cross-functional study teams. Provide regular project status updates and communicate key milestones. Participate in governance meetings and sponsor-facing discussions. Escalate risks proactively and drive solutions to keep projects on track. Clinical Operations Collaboration Partner closely with: Clinical Operations Data Management Biostatistics Clinical Science Assessment Science Project Management Technology Vendors Sponsors Ensure alignment across all stakeholders throughout study execution. Contribute to broader project plans to support successful study delivery. Support study teams in understanding eCOA processes, timelines, and best practices. Licensing, Copyrights & Translations Manage assessment licensing and copyright procurement activities. Coordinate with copyright holders and key opinion leaders as required. Oversee scale and instrument translations supporting global clinical trials. Partner with translation vendors to ensure high-quality multilingual implementations. Manage associated timelines, documentation, and vendor deliverables. Risk Management & Quality Oversight Identify project risks and develop mitigation strategies. Monitor study health, timelines, and quality metrics. Ensure compliance with SOPs, work instructions, sponsor requirements, and industry regulations. Maintain ongoing project documentation and contribute to Trial Master File (TMF) readiness. Support internal audits, sponsor audits, inspections, and quality initiatives. Pr
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