Clinical Data Management
About the Role
Roles & Responsibilities
• Serve as Data Operations Coordinator (DOC) for a single protocol with fewer than 5 operations staff or manage 15+ easy to moderately complex central laboratory studies under guidance
• Act as a lead for specific CDM tasks such as clinical data coding, database testing, or database design (non-complex programming)
• Serve as back-up to DOC or DTL when required
• Perform data review and identify data discrepancies
• Write, manage, and resolve data clarification forms (DCFs)
• Lead or support database audit activities
• Develop, test, and maintain clinical databases and edit specifications
• Perform testing of data management programming activities
• Conduct clinical data coding activities as assigned
• Ensure compliance with SOPs, work instructions, and CDM standards
• Maintain effective communication and collaboration with CDM team members and stakeholders
Qualification
• Bachelor’s degree in Clinical, Biological, Mathematical Sciences, or related field
• Equivalent combination of education, training, and experience may be considered
Skills
• Exposure to medical terminology
• Strong organizational, communication, and computer skills
• Good leadership and coordination abilities
• High attention to detail with ability to work independently
• Strong problem-solving skills and initiative
• Ability to build and maintain effective working relationships with team members, managers, and clients
About the Organization
IQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights, enabling life sciences and healthcare companies to accelerate the development and commercialization of innovative medical treatments and improve patient outcomes worldwide.
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