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Derks & Derks B. V. - Utrecht
Offer working at a quality-oriented biopharmaceutical company a challenging job with a lot of responsibilities Position As a Clinical Study Lead you- Volledige vacature bekijken
Yacht - Eindhoven
Functieomschrijving QMS Manager Start Date:ASAP Duration of the Assignment: 1 year Location: HTC Functieomschrijving QMS Manager Start Date:ASAP Duration of the Assignment: 1 year Location: HTC The QMS Manager is crucial for- Volledige vacature bekijken
Freelance Medical Writer Life Sciences)
Yacht
the Medical Writer may include, but are not limited to, the following: Works independently to write and edit clinical study reports, Investigator’s Brochures, Clinical Trial Results postings, annual reports, and other clinical 8 uur geleden - Volledige vacature bekijken
Qserve Group via Talent - Arnhem
biomedical engineering or similar);3 – 5 years experience as Clinical Project Manager (CPM);Significant experience with study start-up, ethics committee (EC) and competent authority (CA) submission, site- Opslaan
Brand Marketing Intern, Social Media & Content
Catawiki via Talent - Amsterdam
key channelsOwning the social media calendar, scheduling and postingSupporting our Social Media Manager with community management and moderationSupporting our Social Media Manager on paid advertisingIdeating and assisting with- Opslaan
Clinical Trial Manager - - Infectious Disease
Pharmiweb via Talent - The Hague
or life science-related field preferred; Experience in Phases 1-4; Phases 2-3 preferred; Minimum of 2 years of Clinical Trial Management experience, CRO experience preferred; 5+ years of Project Manager / Clinical Trial Manager - Opslaan
Danone Nederland via Talent - Utrecht
RWD): Analyze high-dimensional health datasets collected from digital health tools via real-world/ pragmatic or clinical study settings.Join us in shaping the future of nutritional products through data-driven insights.Main- Opslaan
Sr. Clinical Research Associate
Allucent via Talent - Amsterdam
clinical study sites to assure adherence to protocol, Monitoring Plan, ICH, GCP, SOPs, and applicable regulations and guidelines: Performs efficient site management in line with study budget. Prepares and submits quality Site- Opslaan
Sr. Clinical Research Associate
Allucent via Talent - Amsterdam
activities at clinical study sites to assure adherence to protocol, Monitoring Plan, ICH, GCP, SOPs, and applicable regulations and guidelines: Performs efficient site management in line with study budget. Prepares and submits- Opslaan
Doctoral (PhD) student in Epigenetics of inflammator...
Do we via Academic Positions
researchers and following an individual study plan. For a doctoral degree, the equivalent of four years of full-time doctoral education is required. The research group The Treuter group has a keen interest and a strong29 dagen geleden - Preview - Opslaan
Clinical Research Associate II
Allucent via Talent - Amsterdam
clinical study sites to assure adherence to protocol, Monitoring Plan, ICH, GCP, SOPs, and applicable regulations and guidelines: Performs efficient site management in line with study budget. Prepares and submits quality Site- Opslaan
Regulatory and Start Up Manager (COM)
Iqvia via Talent - Amsterdam
analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required.Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and- Opslaan
Danone Nederland via Talent - Utrecht
size calculations, randomization procedures, and statistical methods for efficacy and safety analyses.Conduct statistical analyses of clinical trial data using proper software packages such as SAS and R.Collaborate with study - Opslaan