TRABAJO CLINICAL SITE TRIALS CONTRACT MADRID, MADRID

Knowledge of clinical trials - knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i...

We offer:·      full-time, permanent contract... understanding of good clinical practice (gcp) standards... life sciences, clinical research, or a related discipline)...

Good understanding of clinical trial contract management...   qualifications bachelor's degree related field req 5-year relevant sponsor or clinical research...

Your responsibilities will include: performing site selection, initiation, monitoring and close-out visits supporting the development of a subject recruitment plan...

• prepares and/or supports contract preparation at a site level (with the exception of countries where there is a specific role dedicated to preparing site contracts)...

’ this role is working in our core clinical site management function... join us in our exciting journey!! we currently require a motivated, creative and enthusiastic...

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our...

• support feasibility, site identification and site documents customization (i... previous experience in clinical trial regulatory submissions...

The project manager is responsible for maintaining the proper project documentation and ensuring compliance with sops and regulatory requirements for clinical...

Milestone one partners with research sites to navigate the complexities of clinical trials seamlessly... our mission is to bring clinical trials to much wider populations...

We offer:full-time, permanent contract... join us in building a diverse and talented team!company description: oxon is a full-service cro providing global scientific...

Visit our careers site to read more about the benefits icon offers... we are currently seeking a senior clinical research associate to join our diverse and dynamic...

Visit our careers site to read more about the benefits icon offers...   our study start up associates are integral in ensuring that physicians at research sites...

Visit our careers site to read more about the benefits icon offers... thorough knowledge of ich gcp and relevant regulations for the conduct of clinical trials benefits...

Achieve and maintain working knowledge of clinical product operation...   location:  on site working schedule (5 days in the office), in our hub in madrid, spain...

“ iqvia is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry...