Remote Clinical Data Associate

Details for the positionare as follows:

• 12-month contract to start.
• 100% remote.

:

• Assess, track and manage end user compliance with operational data governance and system standards.
• Support CMART team in providing status updates on technology implementations to senior leadership.
• Complete data entry into R&D systems.
• Participate in the development of standard operating procedures and/or job aids in support of technology implementations
• Manage resolutions of identified data quality issues for internal systems and vendor data feeds.
• Participate in the development and delivery of end-user training, access and central support model for GCO and GDS managed operational systems and/or inputs into R&D systems (e.g., Veeva Vault Clinical, CTMS, Trial Listings Solution, HCP Engagements etc.)
• In collaboration Clinical Development Services key stakeholders, support data and documentation requests for audits, regulatory inspections and/or other internal purposes.

Required Skills:

• Have experience working with complex databases and ensuring accurate data entry.
• Experience within clinical trial execution and clinical trial lifecycle desired.
• Knowledge of R&D technologies and data sources.
• TMF experience preferred not required.
• Bachelor’s degree with 2 years experience or Associates degree with 4 years’ experience clinical trial data.