Clinical Data Manager II
Job Description:
• The Clinical Data Manager II plays an essential role in the efficient design of project databases, the integration of data from multiple sources, and the reporting and analysis of key study data metrics.
• The incumbent will recommend and drive solutions for database design and data reporting.
• This role is critical for meeting sponsor study data endpoints and requirements.
• Design study CRFs and databases utilizing eCRF library.
• Create study Data Management Plan and deployment roadmap.
• Monitor study timelines and communicate risk.
• Develop database edits, rules, and derivations.
• Prepare tracking reports and metrics.
• Facilitate study team involvement in database development.
• Prepare data extracts and processing for sponsor deliverables.
• Communicate with sponsors regarding study data processes, endpoints, and overall data management process.
• Carryout any other reasonable duties as requested.
Requirements:
• Bachelor’s Degree in Life Science (Biology, Medical Technology, Research Psychology, Math or Health Science or equivalent experience in a related field
• 3-6 years practical work experience in a clinical or technical setting
• Demonstrated experience in team settings to achieve goals
• Demonstrated experience with clinical data management systems
• Experience working with research support or clinical team
• English: Fluent
Benefits:
• Medical, Dental and Vision benefits for you and your family, including Flexible Spending Accounts (FSA) and Health Savings Accounts (HSAs)
• Paid time off policy including holidays and sick time
• Internal growth and development programs & trainings
• 401(k) program, life & accident insurance and disability insurance
Apply Now
Apply Now
• The Clinical Data Manager II plays an essential role in the efficient design of project databases, the integration of data from multiple sources, and the reporting and analysis of key study data metrics.
• The incumbent will recommend and drive solutions for database design and data reporting.
• This role is critical for meeting sponsor study data endpoints and requirements.
• Design study CRFs and databases utilizing eCRF library.
• Create study Data Management Plan and deployment roadmap.
• Monitor study timelines and communicate risk.
• Develop database edits, rules, and derivations.
• Prepare tracking reports and metrics.
• Facilitate study team involvement in database development.
• Prepare data extracts and processing for sponsor deliverables.
• Communicate with sponsors regarding study data processes, endpoints, and overall data management process.
• Carryout any other reasonable duties as requested.
Requirements:
• Bachelor’s Degree in Life Science (Biology, Medical Technology, Research Psychology, Math or Health Science or equivalent experience in a related field
• 3-6 years practical work experience in a clinical or technical setting
• Demonstrated experience in team settings to achieve goals
• Demonstrated experience with clinical data management systems
• Experience working with research support or clinical team
• English: Fluent
Benefits:
• Medical, Dental and Vision benefits for you and your family, including Flexible Spending Accounts (FSA) and Health Savings Accounts (HSAs)
• Paid time off policy including holidays and sick time
• Internal growth and development programs & trainings
• 401(k) program, life & accident insurance and disability insurance
Apply Now
Apply Now