years of clinical monitoring experience, preferred in the field of oncology - Able to independently monitor study sites - Fluent in English and Dutch - Understanding of serious adverse event Are you interested and do want to apply for this role, please fill out your application via the
a research associate you process patient samples and are responsible for performing molecular tests. You are also involved in the optimization of research methods. RESPONSIBILITIES You prepare, perform lab tests, assist with lab equipment and analyse the data afterwards. You
PM-team you will be managing 12-15 projects in the clinical stage of the research, on-site. You will report to the Director of clinical research. RESPONSIBILITIES You will be in charge of setting up the projects, keep track of progress, discuss the results in collaboration
complete. Provide internal communications regarding the important clinical data. Provide safety documentation for the groups that support the safety committee. Assist with logistics for meetings with investigators and other experts. You will participate in improving all processes ...
trial experience or a MSc with experience to a lesser extent (2-3 years) - Experience in management of clinical trials - A background in oncology is a plus - Strong knowledge procedures, regulations and methods - Highly organized and able to keep overview - Able to process high volumes of documents
are in charge of setting up and executing international clinical studies. You report to the Project Management Leader and Scientific Director. RESPONSIBILITIES You are the main contact between industry partners, study groups and several vendors. You coordinate trials ...
development partners to ensure that external development teams provide appropriate and reliable data. RESPONSIBILITIES - Ensure that biowaiver, bioequivalence and clinical parts delivered are appropriate - Identification of deficiencies in such dossiers and clinical data ...
supplies (i.e. GxP, ICH guidelines, Clinical Trial Directive) - Fluent in English Preferred Requirements: - Advanced experience in MS Office applications - Experience in using ERP systems, preferably SAP - Project Management certification (PMP, IPMA) Are you interested and do want
reporting data and trial statuses to senior management. REQUIREMENTS - Over 5 years of clinical trial experience in Class III medical devices - Familiar with EU and FDA regulations - Proven experience in first man studies - Experience/capability to join surgeon team
global supplies at study start to support first subject enrolled per country cluster/depot. RESPONSIBILITIES - Create and maintain project plan to ensure timely clinical study start to support first subject enrolled per country cluster/ depot - Create and maintain study
AML Associate Gdynia NR REF.: 1084439 For our Client, an international company, we are currently looking for a candidates with fluent English, who would like to join AML team in Gdynia.Holding the position of AML Associate you will be expected to investigate and research on risky and rare
Data Analyst Associate Gdynia NR REF.: 1085084 For our Client, an international company, we are currently looking for a candidates with fluent English, who would like to join AML team in Gdynia.Holding the position of Data Analyst position you will be expected to investigate and research
COMPANY Our client is a professional Biotechnology organization, based in Brussel Belgium. The client is a biotech company with an innovative immunotherapy program based on mRNA and after a series of investments are developing into the next phase of their research
expected to investigate and research on risky and rare activities in customer orders and accounts. Additionally you will handling with external parties to verify if order is legitimate. Moreover you will be responsible for dealing carefully with confidential data.To be successful in this role you will need
specification file throughout the life cycle of the clinical trial. -Routing other documents through the companies Quality Systems as per the overall project plan REQUIREMENTS -Bachelor degree or equivalent in logistics, business administration or life science. -Typically 2 ...
relevant industry experience - Excellence in the field of RNA and oncology - Fluent in English - Willing to live in the vicinity of the facility - Sound research techniques Are you interested and do want to apply for this role, please fill out your application via the apply button below
goal is to timely, efficient and effective lead the global design and set up of clinical supply chains for the assigned clinical programs/studies. In order to ensure global supplies at the start of study to support first subject enrolled per country cluster/depot they develop and employ project