2+ years experience in monitoring of medical device trials. - Fluent un French and English, Dutch would be a plus - Strong organizational and time-management skills. - Working knowledge of EU Directives / local regulations / device development, and clinical monitoring procedures ...
Clinical Research Data Manager Warszawa NR REF.: 1100386 Currently for our Client, on of the world's most exciting bio-pharmaceutical companies, we are looking for a Clinical Research Data Manager.If you have minimum 1 year ofData Management experience in the Biotech/Pharma/CRO industry ...
education and ensure the end-user awareness. - Coordinate clinical trainings and lectures with speakers, and ensure the presence of the medical technology for all major congresses and symposiums by developing strong relationships with clinical Bodies like Anaesthesia, ICU, Neonatology and ER ...
tracking, and filing of study documents, and management of the Trial Master File within the clinical projects. In addition, administratively support clinical study staff as required. RESPONSIBILITIES - Under general supervision, accountable for the timely tracking of
QPS Netherlands B.V. in Groningen is onderdeel van een internationale organisatie en voert geneesmiddelenonderzoek uit in opdracht van internationale farmaceutische en biotechnologische bedrijven. Binnen onze divisie Clinical Pharmacology in Groningen zijn wij op zoek naar kandidaten voor de
The GSP (Global Study Planners) that we are hiring now, works 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
SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced ...
you will ensure that all clinical data management tasks in your studies will be delivered to time, quality and cost.As a member of the study team(s), you will provide Clinical Research Data Management (DM) leadership and subject matter expertise to the study team(s) and you will be responsible for
on logistic processes for research and expert panel meetings. REQUIREMENTS - Bachelor or Masters degree in pharmaceutical sciences or related area's - 1 year of experience with the Trial master file, and administrative experience. - Experienced in Microsoft Office
years of experience, and a minimum of 1 years as a Clinical study manager - Fluent in English, additional european languages are a plus - Good knowledge and understanding of ICH-GCP / ISO14155 and the applicable Medical Device regulations Are
clinical master file. - Ervaring met Microsoft Office programma's - Oog voor details en organisatie vaardigheden - Vloeiend in de Engelse taal, Nederlands is een pluspunt Are you interested and do want to apply for this role, please fill out
THE COMPANY Our client is a professional Biotechnology and Pharmaceutical organization, based in Oost-Vlaanderen Belgium. They successfully combine medical research with both academic and pharmaceutical knowledge. Their research and diagnostics
provided. They focus on research and service of generic medicine. ROLE DESCRIPTION You will be functioning in the Quality Assurance team with a focus on the services of the company. You will be supervising the execution of the quality policies ...
associate during absence, holidays or peak periods. Competencies: Customer Focus— dedication to the customer and earns their trust and respect Negotiating—can win concessions without jeopardizing relationships Organizational Agility—knows how to go through the proper channels to get things done Peer
THE COMPANY Our client is a professional Pharmaceutical organization, based in Zuid-Holland Netherlands. They are one of the largest global producers of pharmaceutical products. Their Bacterial Vaccine Research department in Leiden focuses on research
THE COMPANY Our client is a professional Biotechnology organization, based in Limburg Netherlands. They are active in the area of clinical trials manufacturing and cell therapy products for the European market. They are a young company with motivated
medical device industry with experience in batch record review and investigations. • Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and/ or Good Clinical Practice (GCP) knowledge with the ability to interpret and apply in mainly routine cases. • Manufacturing and/or Quality
Years of related Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry with experience in batch record review and investigations. - Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and / or Good Clinical Practice (GCP) knowledge with the