Senior Clinical Data Manager

Job Description:Oversee, lead, manage and provide technical expertise within the assigned projects to ensure that they are executed in an efficient, accurate and timely manner to the Sponsor's satisfaction. Provide fully independent and autonomous leadership of data management services (start up, conduct and close out) across multiple complex global projects/programs. Prepare DM trial documentation (DMP, DB Specifications, Edit check specifications, CCGs, DTAs). Ensure effective UAT is performed. Write external vendor reconciliation specifications for programming reconciliation outputs (e.g. Serious Adverse Events, IRT, Central Laboratory). Oversee data cleaning activities. Monitor project scope, budgets and risks and alert DM Management of any concerns. Requirements:Bachelor's degree or higher in biomedical sciences, life sciences, computer science or related discipline — or equivalent relevant experience Min of 5 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries. Strong knowledge of data management best practices & technologies as applied to clinical trials. Strong understanding of clinical trial process and protocols documents (protocols, statistical analysis plans, CRFs, study reports) and processes. Benefits:Competitive salary Flexible working hours Professional development opportunities Wellness programs