Clinical Data Associate II

The role

The Clinical Data Associate II provides data management support throughout the clinical trial data management process. This role involves database development, testing, and various data management activities under direct supervision.

What you will do

• Support the Lead DM as a back-up and/or team member
• Perform data entry for paper-CRF studies
• Perform quality control of data entry
• Develop CRF specifications from the clinical study protocol
• Assist in building clinical databases
• Conduct database build UAT and maintain documentation
• Specify requirements for all edit check types
• Create, revise, version, and maintain data management documentation
• Train clinical research personnel on study specific CRF, EDC, and project items
• Review and query clinical trial data according to the Data Management Plan

Required qualifications

• Bachelors and/or a combination of related experience
• 2 to 4 years experience
• Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
• Able to handle a variety of clinical research tasks
• Excellent organizational and communication skills
• Professional use of the English language; both written and oral

Nice to have

• Experience in a clinical, scientific or healthcare discipline

Before you apply

• Candidates must be legally authorized to work in the country of employment without employer sponsorship

About the company

Precision Medicine Group is an Equal Opportunity Employer.