Contract research institute daacro offers the following position to qualified candidates:
Study Manager (m, f, d)
biologists, physicians, psychologists
Tasks/Emphasis:
- Administrive and operational tasks in planning and conduct of national and international clinical trials
- Close cooperation with the study team for efficient conduct of trials in compliance with internal and regulatory requirements, especially in regard of the organization and preparation of documents (e.g. management and quality control of the documents)
- Preparation of study documents (case report forms, informed consent, manuals for the staff)
- Compilation and collection of documentation for approval of clinical trials by ethics committees and government agencies
- Procurement of documentation and study material
- Assistance in preparation of monitoring visits and review of monitor reports
- Training the study team
- Creation of publications
- Representing the company in national and international conferences
Requirements:
Academic degree, preferably in medicine, psychology or biology. Training and practice in clinical trials is requested (ICH-GCP knowledge). Important are excellent skills in spoken and written English as well as a high accuracy in scientific and methodical working style.
We anticipate your expressive application:
Contract research institute daacro GmbH & Co KG
Dr. Juliane Hellhammer
Science Park Trier, Max-Planck-Str. 22, 54296 Trier
Phone: +49 (0)651 – 9120 494
E-Mail: hellhammer@daacro.de
Contract research institute daacro offers the following position to qualified candidates:
Study Manager (m, f, d)
biologists, physicians, psychologists
Tasks/Emphasis:
- Administrive and operational tasks in planning and conduct of national and international clinical trials
- Close cooperation with the study team for efficient conduct of trials in compliance with internal and regulatory requirements, especially in regard of the organization and preparation of documents (e.g. management and quality control of the documents)
- Preparation of study documents (case report forms, informed consent, manuals for the staff)
- Compilation and collection of documentation for approval of clinical trials by ethics committees and government agencies
- Procurement of documentation and study material
- Assistance in preparation of monitoring visits and review of monitor reports
- Training the study team
- Creation of publications
- Representing the company in national and international conferences
Requirements:
Academic degree, preferably in medicine, psychology or biology. Training and practice in clinical trials is requested (ICH-GCP knowledge). Important are excellent skills in spoken and written English as well as a high accuracy in scientific and methodical working style.
We anticipate your expressive application:
Contract research institute daacro GmbH & Co KG
Dr. Juliane Hellhammer
Science Park Trier, Max-Planck-Str. 22, 54296 Trier
Phone: +49 (0)651 – 9120 494
E-Mail: hellhammer@daacro.de