CAS Clinical Research II (Advanced Clinical Trial Management)
|Basel, North West Switzerland, Switzerland
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 organisations and regulatory agencies. The program extensively covers the ethical challenges of performing research involving human participants, it teaches project management skills and covers efficiency strategies and the latest technology options, all specifically applied to clinical trial planning and conduct. 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 experience, knowledge and skills and 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 Clinical Trial Practice and Management . The DAS program requires successful completion of the CAS Clinical Research I or an equivalent training program from other universities, successful completion of the CAS Clinical Research II, composition of a diploma thesis and passing of an oral final exam.
This program consists of 4 teaching modules. Teaching modules comprise online courses for self-study and individual completion and classroom training sessions (2-3 days with practical exercises and group discussions). Acquired competencies will be checked by a multiple choice test and completed by homework assignments.
To gain insights into the daily work life in a clinical research profession, a one-week internships (work-shadowings) at a host site within the field of clinical research have to be completed. The host’s main field of activity should be different from the student’s main expertise. It is the responsibility of the student to find a suitable host for the internship.
Completion of the CAS Clinical Research I, CAS Study Nurse/Coordinator or equivalent qualification.
People with minimum 5 years of experience in clinical research working either in academia or in industry (study nurses, study coordinators, clinical research associates, study physicians, assistant physicians, etc.) may apply to be directly admitted to the CAS Clinical Research II program. A certificate in CAS Clinical Research I , CAS Study Nurse/Coordinator or equivalent qualification/experience is recommended.
Continuing in the DAS Clinical Trial Practice and Management program requires documented completion of training equivalent to the CAS Clinical Research I and CAS Clinical Research II programs.
Very good command of oral and written English is a pre-requisite for admission to the program.
This program is conducted in partnership with the European Center of Pharmaceutical Medicine (ECPM). The multidisciplinary teaching faculty consists of national and international experts in clinical research ethics, regulatory sciences and the different fields of operational clinical research.
Mareike Gräter Training and Education Departement of Clinical Research (DKF), University of Basel c/o University Hospital Basel Spitalstrasse 8/12 CH-4031 Basel
email@example.com Tel. 0041 (0)61 556 59 76
Available Mon-Thu 08.30h - 13.30h
Fees include course materials, provisions during coffee/tea breaks and overhead fees. The course fee will be collected in two equal tranches approximately 6 months apart.
The Department of Clinical Research (DKF) offers training grants for members of DKF clinical research groups . Applications for training grants can be submitted when registering for the program.
Cancellation and withdrawal
Online training material will be available approximately one month prior the respective classroom training.
The course provider will comply with any safety measurements required by Swiss authorities, the University of Basel, and the University Hospital Basel. If necessary, classroom training will be adapted to online/virtual sessions.
The next course cycle will be starting in autumn 2024
Course certificates will be issued after successful completion of the module tests, submission of all homework assignments and submission of the work-shadowing report.
The next course cycle will start in autumn 2024. Please click here if you would like to be informed about details on the next course.
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