GCP Clinical QA Specialist – Lead Audits

2 settimane fa


Viù, Italia Philogen S.P.A. A tempo pieno

A biotechnology company located in Siena, Italy is seeking a Clinical Quality Assurance Specialist to ensure compliance with GCP and clinical protocols. The role includes responsibility for maintaining compliant systems and conducting internal audits. Ideal candidates will have a scientific background, experience in clinical quality oversight, and strong English skills. This is an opportunity to join a dynamic team focused on quality in clinical trials.#J-18808-Ljbffr



  • Viù (TO), Italia Philogen S.P.A. A tempo pieno

    A biotechnology company located in Siena, Italy is seeking a Clinical Quality Assurance Specialist to ensure compliance with GCP and clinical protocols. The role includes responsibility for maintaining compliant systems and conducting internal audits. Ideal candidates will have a scientific background, experience in clinical quality oversight, and strong...


  • Viù, Italia Philogen S.P.A. A tempo pieno

    Philogen is looking for a "Clinical Quality Assurance Specialist (GCP)".The position will be responsible to assess compliance with SOPs, GxP, European regulations, local regulations and guidelines, and clinical study protocols.This position will collaborate with other functions in the Clinical Department.In particular the successful candidate will be...


  • Viù, Italia Philogen S.P.A. A tempo pieno

    Philogen is looking for a “Clinical Quality Assurance Specialist (GCP)”. The position will be responsible to assess compliance with SOPs, GxP, European regulations, local regulations and guidelines, and clinical study protocols. This position will collaborate with other functions in the Clinical Department. Responsibilities Maintain GCP / ICH compliant...


  • Viù (TO), Italia Philogen S.P.A. A tempo pieno

    Philogen is looking for a "Clinical Quality Assurance Specialist (GCP)". The position will be responsible to assess compliance with SOPs, GxP, European regulations, local regulations and guidelines, and clinical study protocols. This position will collaborate with other functions in the Clinical Department. Responsibilities Maintain GCP / ICH compliant...


  • Viù, Italia Altro A tempo pieno

    Philogen is looking for a “Clinical Quality Assurance Specialist (GCP)”. The position will be responsible to assess compliance with SOPs, GxP, European regulations, local regulations and guidelines, and clinical study protocols. This position will collaborate with other functions in the Clinical Department.ResponsibilitiesMaintain GCP / ICH compliant...


  • Viù, Italia Altro A tempo pieno

    Philogen S.p.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti-tumor therapies, is looking for a highly motivated and qualified Process & Computer System Validation Specialist (Gcp)RoleThe resource will join the QA department and will be responsible for the validation and maintenance of the...


  • Viù, Italia Altro A tempo pieno

    Philogen S.p.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti-tumor therapies, is looking for a highly motivated and qualified Process & Computer System Validation Specialist (Gcp)Role The resource will join the QA department and will be responsible for the validation and maintenance of the...


  • Viù, Italia Philogen S.P.A. A tempo pieno

    Philogen S.p.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti-tumor therapies, is looking for a highly motivated and qualified Process & Computer System Validation Specialist (Gcp) Role The resource will join the QA department and will be responsible for the validation and maintenance of the...

  • Toscana

    2 giorni fa


    Viù, Italia Philogen S.P.A. A tempo pieno

    Philogen S.P.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti-tumor therapies, is looking for a highly motivated and qualifiedProcess & Computer System Validation Specialist (Gcp) RoleThe resource will join theQA departmentand will be responsible for the validation and maintenance of the company's...


  • Viù, Italia Altro A tempo pieno

    POSITION SUMMARY The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO 14155, ICH / GCP guidelines, Teleflex procedures and IRB / EC policies and procedures). The Senior CRA conducts monitoring visits as identified by...