QPS is a GLP/GCP-compliant contract research organization (CRO) supporting discovery, preclinical and clinical drug development. We provide quality services to pharmaceutical and biotechnology clients worldwide. Our linearly integrated core competencies include:- Preclinical and clinical drug metabolism and pharmacokinetics (DMPK)- Bioanalysis- Early clinical research- Translational medicineFounded in 1995, QPS has bioanalysis and preclinical testing facilities at its Newark, Delaware, headquarters and at its Asia facility in Taipei, Taiwan. An early-phase clinical facility is headquartered in Springfield, Missouri, USA, . Regional business development offices are maintained on the East Coast, West Coast, Midwest, Taipei, Taiwan, and Groningen, The Netherlands.Tasks and responsibilities- General management of department of Project Operations- Member of the QPS Netherlands (Clinical Pharmacology Unit) Management Team and within this team involved in development and management of mid-term strategy for the CPU in order to improve or maintain the profitability of the CPU- Responsible for leading and managing the project execution of all research (clinical phase I and IIa) projects within QPS Netherlands CPU- Leading team of Project Managers, Associate Project Managers, Clinical Study Coordinators, Clinical Trial Assistants, Recruitment Managers, Project Managers Patient Recruitment and Clinical Data Assistants (currently: 18 staff; whereof 13 direct reports)- Responsible for the design and assurance of organizational structure and processes (GCP, ICH, GMP, applicable laws)- Responsible for judgment of feasibilities of request of proposals, generation and review of cost calculations, pricing of quotes, and budget control of the research projects- Responsible for budgeting, planning and control of the department budget- Responsible for adequate allocation of resources, such as staffing, equipment and facilities

Tasks and responsibilities- Project planning- General organization of clinical projects- Start up, organize and support of clinical project teams- Support of data management and consultancy projects- Writing of clinical protocols, reports, CRFs, informed consents- Communicate with sponsors and other third parties- Pre and post calculation of projects

Tasks and responsibilities- Project planning- General organization of clinical projects- Start up, organize and support of clinical project teams- Support of data management and consultancy projects- Writing of clinical protocols, reports, CRFs, informed consents- Communicate with sponsors and other third parties- Pre and post calculation of projects

Tasks and responsibilities- Daily management of department of Recruitment and Screening- Budget control

Tasks and responsibilities- Project planning- General organization of clinical projects- Writing of clinical protocols, reports, CRFs, informed consents- Communicate with sponsors and other third parties- Pre and post calculation of projects

Tasks and responsibilities- Project planning- General organization of clinical projects- Writing of clinical protocols, reports, CRFs, informed consents- Communicate with sponsors and other third parties- Pre and post calculation of projects