Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and
.Who we areWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and
What you will doConduct all types of visits site qualifications, initiation, interim monitoring, site management and study close-out visitsReview study subject
Job DescriptionThe job purpose is to develop and apply analytical methods to detect impurities in final products and drug substances while ensuring regulatory
Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and
What you will doConduct all types of visits site qualifications, initiation, interim monitoring, site management and study close-out visitsReview study subject
Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and
When our values align, there's no limit to what we can achieve. We are currently looking for Regulatory Affairs Professionals experienced in Clinical Trail
.Who we areWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and
.**Reference: 23-174_SS_AO****IDIBELL **is looking for a Research Nurse for the USRC****About the research group**The clinical research support unit (Unitat de
Your responsibilities will includen (and not be limited to):- Reviewing and/or approving all documents following analytical method development (analytical
What you will doConduct all types of visits site qualifications, initiation, interim monitoring, site management and study close-out visitsReview study subject
.If you are an experienced **Clinical Trial Manager **who is passionate about oncology research and looking to join a highly skilled and knowledgeable team,
**Onsite** **Clinical Research Assistant / Clinical Trial Assistant - part time contract (12h/week) for 12 weeks with IQVIA. Site is located in
.Why Patients Need YouWe're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local
What you will doConduct all types of visits site qualifications, initiation, interim monitoring, site management and study close-out visitsReview study subject
What you will do Conduct all types of visits site qualifications, initiation, interim monitoring, site management and study close-out visits Review study
What you will doConduct all types of visits site qualifications, initiation, interim monitoring, site management and study close-out visitsReview study subject
Due to ongoing global expansion, Innovaderm is looking to hire a Regulatory Affairs Specialist. In this position, you will be responsible for preparation and
.Due to our continued growth, we are recruiting for trainee Clinical Research Associates to join our team. IQVIA Biotech is unique division specialising in