August 8
🏡 Remote – New York
• Responsible and manages all aspects of the clinical trial data management process from study start up to post database lock for assigned projects. • Primary Data Management contact for assigned projects, ensuring task continuity and timely execution. • Oversee project data entry process including development of data entry guidelines and training. • Develop CRF specifications from the clinical study protocol. • Conduct database build UAT and maintain quality controlled documentation. • Review and query clinical trial data according to the Data Management Plan. • Liaises with third-party vendors in project manager capacity.
• Bachelors and/or a combination of related experience • 8+ years’ experience for a Sr. Clinical Data Manager and 10+ years for a Principal Clinical Data Manager • 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 • Experience in utilizing various clinical database management systems • Broad knowledge of drug, device and/or biologic development and effective data management practices • Strong representational skills, ability to communicate effectively orally and in writing • Strong leadership and interpersonal skills • Ability to undertake occasional travel
• Discretionary annual bonus • Health insurance • Retirement savings benefits • Life insurance • Disability benefits • Parental leave • Paid time off for sick leave and vacation
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