Beschreibung des Angebots
The goal of this program is to impart information and skills necessary for the variety of management and leadership positions in different clinical research settings such as academia, pharmaceutical, medical device or biotech industry, as well as clinical research organizations and regulatory agencies. The program extensively covers the ethical challenges of performing research involving human participants, it teaches project management skills specifically applied to clinical trial planning and conduct and covers efficiency strategies and the latest technology options. Further topics are regulatory and legal requirements in international research settings and enhanced communication and conflict management skills.
This continuing education program has been designed to meet the needs of experienced clinical research professionals from industry and academia (study/trial coordinators, study /trial managers, study physicians, clinical trial/research associates, clinical monitors, study nurses, etc.), as well as experienced members of ethics committees or regulatory agencies. It provides an opportunity for advancing technical and (inter)personal experience, knowledge and skills as well as for professional networking in the environment of clinical trial practice and management.
Students interested in a higher level of postgraduate education in this field may consider completion of the program Diploma of Advanced Studies DAS in Clinical Trial Practice and Management. The DAS program requires successful completion of the CAS in Clinical Research I or an equivalent training program from other universities, successful completion of the CAS in Clinical Research II, composition of a diploma thesis and passing of an oral final exam.
Aufbau der Ausbildung
This program consists of 5 face-to-face teaching modules (3-days in length except the final module, which is 2-days). Each module comprises lectures, practical exercises, group discussions and self-directed learning. Acquired competencies will be checked by a multiple choice test and completed by homework assignments.
To gain insights into practical aspects of the daily work life in a clinical research profession a one-week internship (work-shadowing) at a host site involved in any field of clinical research has to be completed. This work-shadowing has to be organized individually.
People with experience in clinical research working either in academia or in industry (study nurses, study coordinators, clinical research associates, study physicians, assistant physicians, etc.).
CHF 4'000.- for employees from the University Hospital Basel and the University Basel
CHF 5'000.- for regular participants
Fees include course documentation and provision during coffee/tea breaks
- Certificate of Advanced Studies CAS
Certificate of Advanced Studies in Clinical Research II (Advanced Clinical Trial Management), University of Basel
Ort / Adresse
- Basel (BS)
University Hospital Basel
Modules will take place in 2016. Work-shadowing week can be scheduled individually.
Auskünfte / Kontakt
Marie Mi Bonde Hansen, PhD
University Hospital Basel
Clinical Trial Unit
Training and Education
Tel. +41 61 328 51 47
Der Studiengang ist Teil der Advanced Studies, der berufsbegleitenden Weiterbildung der Universität Basel.