Job description
Responsibilities: * Responsible for ensuring the completeness, quality, and integrity of the Clinical Trial data. * Ensure data quality and consistency according to applicable regulatory requirements, standard operating procedures (SOPs), processes and data standards. * Ensure all data management activities to be compliance with GCP, relevant regulatory requirements and SOP/WI (work instructions) of company and/or Sponsor. * Ensure acknowledge, follow and to be consistent with company policies and procedures. * Act as Lead Data Manager for multiple ongoing clinical studies. * Ability to train junior Clinical Data Managers and assign tasks as required. * Ability to create and maintain DM Timelines. * Responsible for leading team activities with the sponsor, creating and maintaining the Global Library and maintaining eTMF and TMF (where applicable). Requirements: * Bachelor’s Degree or higher in a life science or related field * Minimum of 7 years of data management experience in a pharmaceutical or clinical research setting
Job Types: Full-time, Contract
Schedule:
- 8 hour shift
- Day shift
Work Location: Remote
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