• Tempo indeterminato
  • Lombardia
Dettagli

A leading international pharmaceutical company is looking for a Clinical Data Management Specialist.

Ruolo
  • Implementation and supervision of data management start-up, maintenance and completion activities and relevant documentation (data management plans, data validation plans and other study specific procedures) within assigned clinical trials
  • Provision of adequate sponsor oversight to data management processes performed by CRO’s and/or external data providers (e.g. for ePRO data, laboratory data)
  • Monitoring and supervision of the set-up, validation and maintenance of CDMS systems (eTools like EDC, IRT) including Sponsor testing activities and archiving of relevant trial documentation
  • Develop and maintain Clinical Database Build specifications (CDISC based)
  • Ensure adherence to GCP, regulatory guidelines, standard processes and SOPs
  • Attending internal/CRO meetings as required, interacting and collaborating directly with the assigned project manager and other specialty team members (clinical, programming, statistics, drug safety, drug supply etc.) to provide data management support to ensure consistent data handling and quality
Profilo
  • Master’s Degree in Scientific Subjects, Mathematics, Statistics; Fluency both in oral and written English;
  • OFFICE SAS (Opt); CDISC;
  • Previous Experience of at least 3-5 years in a similar role.
Offerta

Full Time, Tempo Indeterminato

Per candidarti invia i tuoi dati a selezione@arethusa.it