PSI CRO AG
Healthcare Insurance âą Pharmaceuticals âą Science
PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.
Clinical Trials Data Manager
Job not on LinkedIn
September 18
PSI CRO AG
Healthcare Insurance âą Pharmaceuticals âą Science
PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.
đ Description
âą Track database set-up, testing, maintenance and data entry âą Communicate with clients, project teams and vendors on data management matters âą Review study documents, design and develop project specific guidelines and instructions âą Design eCRF, Data Management and Data Validation Plans and test EDC databases âą Ensure data entry, follow-up and validation, including manual CRF review and SAE reconciliation âą Code medical data âą Track and report metrics leading to database lock âą Coordinate the processing, dispatch and archiving of CRFs/queries âą Maintain Clinical Data Management working files âą Perform database QC checks, prepare and attend audits âą Train site staff and project teams on CRF completion and data management topics
đŻ Requirements
âą College/University degree (Life Science, Pharmacy degree is a plus) âą Based in Brazil âą Demonstrated experience of managing clinical or medical data âą Full working proficiency in English âą Experience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm) âą Proficiency in MS Office applications âą Organisational and time management skills âą Ability to work independently and multi-task âą Please submit your CV in English
đïž Benefits
âą Employees can work remotely
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