you’ll be involved in: - Assisting the project manager or clinical team manager on assigned projects - Support line manager - Travel 60-80% on average REQUIREMENTS - BSc/MSc in a science related field - +- 5 years experience in Clinical research with a high level
As a CRA you will visit and monitor clinical study sites where you will be in touch with patients, nurses and doctors. You will be part of international clinical studies. This position is on permanent basis. RESPONSIBILITIES You gather all research data
time, permanent position that can be worked homebased. RESPONSIBILITIES - monitor Clinical study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines - All aspects of site management as prescribed in the project plans ...
site monitoring according to SOPs, GCP, and ICH guidelines, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files RESPONSIBILITIES - monitor Clinical study sites independently
THE COMPANY Our client is a professional Biotechnology and Pharmaceutical organization, based in Netherlands. They are a Research Organisation with influence in over 50 countries worldwide. They are active in the medical devices industry, biotechnology
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
patient sample receipt - biobanking of immune cells derived from clinical patient material - participate in the maintenance of equipment and lab areas REQUIREMENTS - Bachelor in Laboratory Techniques/Master in Biomedical Sciences or a related field - at least two
policy, SOPs and regulatory requirements. May include international and overnight travelling RESPONSIBILITIES - Monitor on-site and remotely clinical trials. - Review and support site staff to maintain Site Master File(SMF). - Update Clinical Trial Management
team analysis. The position is needed for 6 months at 32 hours per week (0,8 FTE). RESPONSIBILITIES You assist the Clinical Program Manager where you provide critical path analysis, cross functional project plans and provide strategies and schedules to keep all
on a subset of GSP responsibilities and together with the study GSP ensure supplies for our worldwide patients that participating in a clinical trial. This role has narrow scope in a complex logistical environment that is ideal for people without any or extensive working experience. The supportive Global
participating in a clinical trial. This role has narrow scope in a complex logistical environment that is ideal for people without any or extensive working experience. The supportive Global Study is point of contact for dedicated processes and works with global peers, customers and supplies to improve the
product that is needed for the company's clinical trials. ROLE DESCRIPTION We have a team of Global Study Planners in two locations; one in the US and one Breda, in the Netherlands. The Global Study Planners (GSP) handle medium-high complex
planning and Logistics Service Providers teams Sales Order management: - Create and Process Clinical Drug Shipments - Create or coordinate obtaining of necessary shipping documentation Stock Transfer Order Management (STOs): - Schedule and Process STOs - Create or coordinate obtaining of necessary
THE COMPANY Our client is a professional Pharmaceutical organization, based in Noord-Brabant Netherlands. I am looking for an associate for the global clinical supply chain department. In this position you will have a supportive role to the Global Supply
recruitment purposes and implementation of recruitment campaigns as well as assisting in the increase of the unit awareness - Recruiting, orienting, scheduling and may ensure compensation for all volunteers and subjects participating in clinical research studies; - Assisting in different secretarial ...
Background as Nurse is much appreciated - People management experience is much appreciated; - Clinical research/Clinical study experience (not mandatory) - IT skills : Must have excellent working knowledge of computers, and familiar with Microsoft Office Applications; - Good knowledge of all applications