
Associate eCOA Manager
Posted 6 days ago

Posted 6 days ago
This is a fully remote position, open to applicants in United Kingdom.
• Provide oversight for project management from maintenance to eCOA decommissioning.
• Ensure deliverables, timelines, and work completion adhere to Worldwide SOP standards.
• Analyze and identify trends within studies.
• Collaborate proactively with eCOA vendors and study teams to meet study-specific needs.
• Relay eCOA project activity updates to internal and sponsor study teams.
• Act as the escalation point for project-related issues pertaining to assigned eCOA studies.
• Coordinate the timely distribution of eCOA project communications, such as status reports, meeting agendas, minutes, and scheduling of project calls.
• Review the overall design of eCOA studies.
• Approve User Requirements Specifications (URS) for any changes in scope following go-live.
• Prepare, assess, and approve site and support materials as well as helpdesk documentation when necessary.
• Conduct financial reviews and manage budgets, including the assessment of change orders.
• Bachelor’s degree in a relevant field or equivalent experience.
• At least 1 year of experience in eCOA and clinical trials.
• Minimum of 1 year of experience in project management.
• Strong client-facing communication skills.
• Proficient in standard office software.
• Self-driven with a positive contribution to team dynamics.
• Exceptional attention to detail.
• Capability to prioritize and manage multiple projects at once.
• Ability to exercise sound independent judgment and take initiative.
• Skilled at making effective decisions in a fast-paced, dynamic environment.
• Adaptable to new technologies, concepts, and processes.
• Highly organized with a focus on detail and service.
• Outstanding project management abilities.
• Ability to lead and comprehend policies, procedures, financial, and leadership principles.
• Proven knowledge of operational aspects of Phase I-IV clinical research trials.
• Understanding of the Software Development Life Cycle (SDLC).
• Familiarity with eCOA topics, including designs and scales.
• Experience in Contract Research Organizations (CRO) or the pharmaceutical industry is required.
• Proficient in English for writing, speaking, and understanding daily business communications.
• Willingness to travel domestically and internationally as required.
• Flexibility to work across different time zones when necessary.
• Supportive and cohesive teams with approachable leadership.
• Opportunities for mentorship and training.
• Potential for internal promotions and career growth.
• Diverse and inclusive workplace culture.
• Flexible remote work options.
• Possibility of domestic and international travel.
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