IXRS Validation Lead Job in North Carolina (NC), Other Career, Full Time Jobs in Covance, Inc. a division of LabCorp®
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IXRS Validation Lead job in Raleigh-Durham

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Covance, Inc. a division of LabCorp® jobs
North Carolina (NC), Raleigh-Durham
Job Code:  2018-23791
Employer:  Covance, Inc. a division of LabCorp®
Category:  Other
Job Type:  Full Time

Location
Country:  United States
State:  North Carolina (NC)
City:  Raleigh-Durham
Map: 
09/06/2018

Description
Job Overview
IXRS Validation Lead

Permanent, salaried
Remote from anywhere in the U.S. or Canada

Responsibilities
- 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.

Education/Qualification
- Degree in a mathematical, computing, life sciences, or related discipline

Experience
- Minimum 2-4+ years of experience in clinical systems such as CTMS, ePRO, IXRS, EDC or an equivalent combination of education and experience to successfully perform the key responsibilities of the job
- Strong oral and written communication skills. Experienced project leader and presenter.
- Proficiency in converting complex technical and business requirements into clear test plan and test cases.
- Understanding of Drug Development and Clinical Trial Processes
- Understanding of Data Management Processes
- In-depth knowledge of Good Clinical Practices
- Understanding of Clinical Research System Development Lifecycle
- Must have sound problem resolution, judgment and decision-making skills.
- Ability to prioritize tasks effectively and manage multiple projects simultaneously. Education/Qualifications
Education/Qualification
- Degree in a mathematical, computing, life sciences, or related discipline Experience
Experience
- Minimum 2-4+ years of experience in clinical systems such as CTMS, ePRO, IXRS, EDC or an equivalent combination of education and experience to successfully perform the key responsibilities of the job
- Strong oral and written communication skills. Experienced project leader and presenter.
- Proficiency in converting complex technical and business requirements into clear test plan and test cases.
- Understanding of Drug Development and Clinical Trial Processes
- Understanding of Data Management Processes
- In-depth knowledge of Good Clinical Practices
- Understanding of Clinical Research System Development Lifecycle
- Must have sound problem resolution, judgment and decision-making skills.
- Ability to prioritize tasks effectively and manage multiple projects simultaneously.
ref: (2018-23791)
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