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Provide timely and professional ongoing management of clinical trial data with respect to cost, quality and timelines for assigned trials managed within Clinical Data Management. Ensure consistently high quality data available for analysis and reporting.
As CDM provide data management input on Clinical Trial Teams. May have the role of TDM on small, low complexity trials
Reviews and contributes to preparation of protocols, specifically related to the Visit Evaluation Schedule (VES), Study Design and Data Management section
Gives input to DHP and DRP for assigned trials. Responsible for the development of these documents if assigned the role of TDM
Participates in the preparation of training materials for investigator meetings
Disseminates study-level information either to the TDM (if assigned to a trial as a Data Manager) or to the Clinical Trial Team (CTT) & Program Clinical Data Manager (PCDM) if assigned the role of TDM
Timely and high quality completion of Data Management deliverables according to established objectives, including: DHP/DRP, CRF Design, CCGs, UAT of eCRF, Snapshots and Database Locks (interim or final)
University or college degree in life science, computer science, pharmacy, nursing or equivalent relevant degree.
Ideally 3 years experience in Drug Development with at least 2 years in Clinical Data Management
Market-leading salary will be offered depending on actual level of experience and skills
Permanent contract of employment with full DOCS benefits
Full comprehensive training program