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Sr Clin Data Coordinator
IQVIA
Full time
1+ years
Not Disclosed
Thane, India
Post Date: Feb 19, 2024
End Date: Apr 19, 2024
Expired
1+ years
Not Disclosed
Thane, India
Post Date:Feb 19, 2024
End Date: Apr 19, 2024
Skills:
clinical research
Operations
Clinical Trial
Inspection
Job Description:
Responsibilities
Manage delivery of projects through full data management study life-cycle (with minimal guidance).
With guidance from DTL or Manager, manage project timelines and quality.
Determine resource needs.
Identify out-of-scope work.
Serve as Data Operations Coordinator or Data Team Lead (with guidance).
Perform comprehensive data management tasks including data review, writing and resolving data clarifications.
Perform database designer activities for technologies not requiring extensive programming.
Perform comprehensive quality control procedures.
Independently bring project solutions to the CDM team.
Solve issues through using the global issue escalation/communication plan.
Consult with Standards Group for process issues.
Communicate ideas for process improvement.
Assist in developing and implementing new technology.
Understand and comply with core operating procedures and working instructions.
Meet objectives as assigned.
Develop and maintain good communications and working relationships with CDM team.
Interact with CDM team members to negotiate timelines and responsibilities.
Qualification & Experience
Bachelor's Degree Health, clinical, biological sciences, or related field Req
1 year clinical trials experience in function similar to DM; or equivalent combination of education, training and experience Req
Good understanding of clinical drug development process. Intermediate
Background in medical terminology, Pharmacology, Anatomy, and Physiology. Intermediate
Job Overview
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Salary
Not Disclosed
Role
Executive or Officer
Area of Practice
Clinical Data Management
Experience
1+ years
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