The Role
Lead and manage all Clinical Data Management deliverables for global trials (Phases I-IIIb). Develop and implement risk-based strategies for data collection, cleaning, and quality assurance. Ensure data accuracy and integrity through comprehensive review and validation. Represent Clinical Data Management on the Core Trial Team and serve as the main contact for data-related tasks. Oversee the quality and submission readiness of clinical databases and data packages (e.g., CDISC).You
Bachelor’s or master’s degree in a scientific or technical field, preferably in life sciences or data management. Strong experience in clinical data management within the pharmaceutical, biotechnology, or healthcare industry. Commitment to continuous learning and bringing fresh insights to drive innovation and process improvement. Proven ability to lead and manage end-to-end data management activities and coordinate global teams in a matrix organization. Strong project management, communication, collaboration, and problem-solving skills.The latest news, articles, and resources, sent to your inbox weekly.
A great opportunity has opened within the Data Monitoring, Management and Innovation department to further strengthen our Clinical Data Management team.As a Senior Clinical Data Manager, you will play a crucial role in managing and overseeing clinical data management activities within the organization. You will be responsible for ensuring the...
Merck KGaA, Darmstadt, Germany Feltham
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting...
MAI Fortrea Development Limited
Position Summary:The Senior Clinical Data Manager/Principal Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up to post database lock for assigned projects. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed....
Precision Medicine Group
Oracle Life Sciences is a leader in cloud technology, pharmaceutical research, and consulting, trusted globally by professionals in both large and emerging companies engaged in clinical research and pharmacovigilance, throughout the therapeutic development lifecycle, including pre- and post-drug launch activities. With more than 20 years’ experience, Oracle Life Sciences is...
Oracle
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting...
MAI Fortrea Development Limited Maidenhead
Requisition Number7581Employment Type:RegularWho we areWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience,...
Worldwide Clinical Trials
