Support the Lead DM as a back-up and/or team member, ensuring continuity, responsiveness, and that
May perform data entry for paper-CRF studies, as needed
May perform quality control of data entry
May provide input into timelines. Ensure that clinical data management deadlines are met with
Assist in developing CRF specifications from the clinical study protocol and coordinate the
May assist in building clinical databases

🎯 Requirements

5+ years' experience
Bachelor's and/or a combination of related 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

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