Bioclever CRO (An Astrum Company)
Mireia Vega Capmany is a seasoned professional in clinical data management, currently serving as Lead Clinical Data Manager at Bioclever CRO since March 2014, where expertise encompasses protocol development, data management documentation, CRF design, and data cleaning activities. Prior to this role, Mireia held positions as Senior Clinical Data Manager and Clinical Data Manager, gaining extensive experience in developing Data Management Plans, validation, data coding, and training services. Additional experience includes managing eCRDs for various clinical phases at onmedic Networks and research roles focused on genomic and nanotechnology applications. Mireia’s educational background includes a degree in Biotechnology from Universidad de Vic and specialized training in clinical trial design from The Johns Hopkins University and CDISC fundamentals.
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Bioclever CRO (An Astrum Company)
Since 2005 offering Clinical Research, Monitoring, Pharmacovigilance, Biometry & Regulatory Solutions to the global life science industry Full Service CRO and solutions. BioClever CRO offers a full range of clinical trial research development in the areas of pharmaceutical and medical device development services Phase I, II, III & IV Excellence in Clinical Trials conduction. We work with the highest quality standards, on time, and respecting the budget ISO: 9001 Certification. We’re fully ISO 9001 certified and focus all those best practices and knowledge, gained through years of successful audit inspections and approvals, on meeting your requirements. People. Success depends on the quality and motivation of our people. Our costumer approach allows us to provide clients with the highest quality services covering all aspects of clinical trial. 100% oriented to the internal and external client, we have a personnel turnover of less than 3% a year. Flexibility. We adapt to the specific needs and priorities of our clients.