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Clinical Research I (Clinical Trial Planning and Conduct)

CAS

Universität Basel UNIBAS

Catégories
Lieu de formation

Bâle (BS)

Langue d'enseignement

anglais

Type de formation

Hautes écoles universitaires HEU - Formation continue: formations longues

Modalités temporelles

À temps partiel

Thèmes de formation

Santé, soins, médecine

Filières d'études

Médecine humaine

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7.724.4.0

Mise à jour 19.06.2024

Description

Description de la formation

The goal of this program is to impart information and skills necessary to successfully start or enhance a new career as a clinical research professional. The program provides a profound background on the development of new therapies with a focus on drug development, covers key ethical aspects of conducting research involving human participants, teaches the regulatory and legal requirements of performing clinical studies and finally thoroughly explains the planning and performance competences of conducting clinical trials.

This continuing education program has been designed to meet the needs of young clinical research professionals from industry and academia (study nurses, study coordinators, study physicians, clinical trial/research associates, clinical monitors), as well as for new members of ethics committees. Furthermore, it provides an opportunity for graduates from life sciences and medical schools to gain a comprehensive understanding of the phases of clinical research and the practical aspects of clinical trial planning and conduct.

Students who are interested in a broader training on operational aspects of clinical trials including management and leadership skills may be interested in complementing their knowledge through an additional CAS Clinical Research II (Advanced Clinical Trial Management). After successful completion of both the CAS Clinical Research I and the CAS Clinical Research II, it is possible to receive the Diploma of Advanced Studies (DAS) Clinical Trial Practice and Management by composition of a diploma thesis and passing a final oral examination.

Plan de la formation

This program consists of 3 modules. Each module comprises an online training for self-study and individual completion and a classroom training (2-3 days with practical exercises and group discussions).

Acquired competencies will be checked by multiple-choice tests and homework assignments. To gain insights into the daily work life in a clinical research profession, a one-week internship (work-shadowing) at a host site within the field of clinical research has 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.

Admission

Conditions d’admission

People working in any area of clinical research either in academia or in industry (study nurses, study coordinators, clinical research associates, study physicians, assistant physicians, etc.)

This program has been specifically developed for

  • Candidates with a science or medical degree (minimum Bachelor's degree)
  • Candidates without a university degree but with a professional qualification ("abgeschlossene Berufsausbildung" or similar) and at least two years of practical work experience in clinical research (based on "sur-dossier" decisions)

Very good command of oral and written English is a pre-requisite for admission to the program.

Coûts

CHF 6'600.-

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 of CHF 1’000 for members of the DKF clinical research groups. A list of DKF clinical research groups can be found here. Applications for training grants can be submitted when registering for the program. Please note, that training grants can only be offered to DKF clinical research group members, who are working at the group leaders’ local study center.

Diplôme

  • Certificate of Advanced Studies CAS

Certificate of Advanced Studies (CAS) Clinical Research I (Clinical Trial Planning and Conduct), University of Basel

Infos pratiques

Lieu / adresse

  • Bâle (BS)

Universitätsspital Basel
Hebelstrasse 10
4031 Basel

Hörsaal 6 (ZG), Markgräflerhof (beim Blutspendezentrum)

Déroulement temporel

Durée de la formation

approx. 8 months

Modalités temporelles

  • À temps partiel

Langue d’enseignement

  • anglais

Course materials, language of instruction and module tests are in English. Homework and reports may be submitted in English or German.

Liens

Renseignements / contact

Mareike Gräter
Training and Education
Department of Clinical Research
University of Basel
c/o University Hospital Basel
Spitalstrasse 8/12
CH-4031 Basel l

Phone +41 61 556 59 76
www.dkf.unibas.ch

Der Studiengang ist Teil der berufsbegleitenden Weiterbildung der Universität Basel.

orientation.ch