the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and Standard Operating Procedures. RESPONSIBILITIES Your responsibility is to perform and coordinate all aspects of the clinical
Project or Planisware knowledge - Clinical trial knowledge/experience - Strong communicator Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Naut van Osnabrugge ...
design, execute and coordinate clinical trials. You will be supervised by a project manager. RESPONSIBILITIES - Monitor on-site and remotely clinical trials - Make sure the clinical trials are compliant with ICH-GCP - Execute clinical trials according to SOPs
and regulatory requirements and study completion on time and within budget. Also you wil monitor sites en keep de ICH-GCP in mind. RESPONSIBILITIES - Monitoring of clinical trials in accordance with ICH-GCP standards - Site management - Developing and
following GCP guidelines. You analyse and report these results to project management. REQUIREMENTS - BSc in a relevant field - 2 years minimum of clinical research experience - Fluent in English and German is required - Detail oriented, precise personality
ROLE DESCRIPTION As Head Clinical Research Neurology you will focus on defining the strategy for clinical research in the Neurology area. The successive applicant will focus mainly on the Early Development stages. He/she has a strong background in Neurology related clinical
or degree as research nurse - SOPs, ICH Guidelines and GCP - 2 years of experience in clinical research - Dutch and English Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Neal Hagen ...
clinical R&D studies by setting up, working out and filing all clinical study documents. This position is on a freelance basis for one year for full time on site. RESPONSIBILITIES You are responsible for all clinical study documents, to make sure that they are
the job; when interested you may design and deliver training to the staff. Other responsibilities and activities you will be working on include: - Preparing for and attending investigator meetings, coordinate those meetings - Ensure integrity of clinical data by maintaining site track records - Drug
- Academic degree in a medical discipline - 2-5 years of experience in management of clinical trials, oncology or tumour research preferred - Strong knowledge procedures, regulations and methods - Highly organized and able to keep a helicopter view - Able to process high volumes of documents and
operations is responsible for recruitment, growth and development of Clinical operations employees. RESPONSIBILITIES -Develops plans to support growth and career development of assigned Clinical Operations employees as well as manage the delivery of quality
current managers have their hands full. This position is a full time position but homebased working is possible for two days per week. RESPONSIBILITIES You will take care of all clinical trials from start until the end. You will set up timelines, take care of
managers have their hands full. This position is a full time position but homebased working is possible for two days per week. RESPONSIBILITIES You will take care of all clinical trials from start until the end. You will set up timelines, take care of budgets and set
work in the Biotechnology, Medical Devices, Government organisations and the Pharmaceutical industry. They have offices in 49 countries and they have more than 21000 employees! They work on Early Development and Clinical Development. ROLE DESCRIPTION
experience - Industry certifications such as CCRA or RAC are preferred - Fluent in English - Clinical / medical devices background is a plus Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Naut van Osnabrugge ...
primary contact person for the local teams within the Clinical Organisation · Create appropriate trial-specific training materials and requirements · Set-up and coordination of Investigator Meetings REQUIREMENTS - Minimum of Bachelor in Life Sciences related field ...