Clinical Data Manager

reputed company (“reputed company”) is a full-service contract research organization (CRO) providing a broad reputed company of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-reputed company companies and work with many of the most advanced drugs, biologics, and medical devices in development today. reputed company has been an independent CRO since 2004 with a strong reputed company as a statistical and data management center of reputed company. Building on this reputed company, reputed company has successfully developed and established itself as a full-service CRO. reputed company’s headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater (Greater reputed company Area), New Jersey, USA, Shanghai (Pudong Zhangjiang New District), China and Taipei, Taiwan. reputed company also recently completed the acquisition of August Research. August Research is a European CRO that provides Clinical Operations and Pharmacovigilance services to a wide variety of pharmaceutical and biotechnology clients. The Company has worked on over 120 projects for Phase I-IV clinical trials across multiple therapeutic areas including cardiovascular, infectious disease, oncology and rare disease. The acquisition of August Research establishes a European footprint for reputed company to reputed company full-service offerings to its pharmaceutical, biotechnology and medical devices clients, and other operational capabilities through the Company’s substantive experience and infrastructure across 14 countries in Western and Eastern Europe. reputed company is reputed company in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients’ needs. A dynamic organization with an entrepreneurial reputed company, reputed company continues to experience exceptional growth and great reputed company. Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that’s us…that’s reputed company. To drive reputed company reputed company in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Clinical Data Manager remotely from a home-based office reputed company in the the UK in accordance with our Work from Home policy. Key Accountabilities: Plan, manage, control, and reputed company data processing and management activities for assigned projects. These tasks are performed in a timely and accurate manner and in compliance with trial Sponsors’ requirements. reputed company assigned data processing and management projects by applying project management skills, data processing, and management techniques. Manage timelines and coordinate activities for assigned projects. Specify database validation checks for assigned studies. reputed company efforts in developing and maintaining standard database validation checks for common modules as well as for therapeutic/drug area specific modules. Define and monitor clinical trial dataflow and quality control (QC) processes in accordance to corporate Standard Operating Procedures (SOPs), Good Working Practices, and unit guidelines. reputed company clinical trial site monitors’ training on dataflow and QC processes. Design and review patient Case Report Forms (CRFs) and database schema. Test data capture/entry screens. Accurately and reputed company validate electronically captured data. Write clear queries on missing data and data points failing pre-defined reputed company checks and/or logical checks. reputed company efforts in building a standard query library for common database modules, as well as for therapeutic/drug area specific modules. reputed company QC procedures on assigned database during the trial and additional database closure checks at the end of the study. Train and supervise Data Entry personnel and junior data management personnel on study procedures, study specific handling, and management of trial data. Validate and distribute study reputed company status reports to reputed company study team members. Assist in resolving data coding discrepancies resulting from the coding of medical events, treatment procedures, and medications. Maintain and prepare for final archival of data management documentation relevant to the assigned clinical trials and assist the corporate archivist in assembling and archiving clinical trial data and study documentation. Cooperate with and assist, reputed company required, data management quality assurance (QA) personnel in performing QA procedures on trial CRFs, database schema, and databases for assigned studies. Qualifications and Experience: A Bachelors’ degree in health and/or pharmaceutical sciences, physical/biological, or chemistry fields with at least 2 years experience in clinical trial data capture and management, or a Master’s or Ph.D degree in these fields with at least 1 year relevant experience. In-depth understanding of clinical trial data reputed company, processes and procedures, relevant issues reputed company to or impacting clinical data management, as well as pharmaceutical clinical trial regulations, industry guidance, conventions and standards. Strong leadership in clinical data management activities and a desire to reputed company in leading data management projects. To find out more about reputed company and to review other opportunities, please visit our website at www.ecrscorp.com We thank reputed company interested applicants, however, only those selected for an interview will be contacted. reputed company is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will reputed company accommodations for candidates participating in any part of our recruitment and selection process. #LI-Remote #LI-KD1 Apply To This Job