Proactively follow-up with customers and third-party vendors to ensure comprehensive understanding of requirements and design in order to provide quality deliverables. Active participation in study team meetings. Review and provide input on requirements and specifications. Create validation documentation – UAT Test Plan, test scripts, and defect tracker. Direct teams during testing execution for initial implementation and updates. Function as point of contact during UAT for team members, triaging and resolving issues as needed. Manage UAT plans and timelines, ensuring that team members adhere to the schedules and timetables for the completion of projects. Advise the team and stakeholders, informing on the processes that will be completed to enable system implementation.
Minimum 2-4+ years of experience in clinical systems
Proficiency in execution of eCOA Test Scripts on Handheld and eDiary devices
Understanding of Drug Development and Clinical Trial Processes
Documentation
Time Management
Analytical skills
Data Management Processes
Clinical Research System Development Lifecycle
Multitasking
Process Improvement
Detail Oriented
Communication Skills
Problem-Solving
According to JobzMall, the average salary range for a eCOA Validation Lead is anywhere from $80,000 to $120,000. This range may vary depending on the company, experience level, and location.
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Covance Inc. is a contract research organization headquartered in Princeton, New Jersey, providing nonclinical, preclinical, clinical and commercialization services to pharmaceutical and biotechnology industries. The company is owned by LabCorp and employs more than 50,000 people in over 60 countries. In 2014, Laboratory Corporation of America- Labcorp, purchased Covance.

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