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Country Study Operations Manager

Pfizer - Rotterdam
sites. Share and escalate plan deviations to Clinical Project Manager and study team. Help to address Significant Quality Events or other quality issues at patient and/or site level. Lead the data integrity and data quality
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Country Study Operations Manager

Pfizer - Eindhoven
sites. Share and escalate plan deviations to Clinical Project Manager and study team. Help to address Significant Quality Events or other quality issues at patient and/or site level. Lead the data integrity and data quality
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Country Study Operations Manager

Pfizer - Nijmegen
sites. Share and escalate plan deviations to Clinical Project Manager and study team. Help to address Significant Quality Events or other quality issues at patient and/or site level. Lead the data integrity and data quality
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Nine Zadelhoff Novartis past heel goed bij mij

Novartis
Nine van Zadelhoff werkt al 15 jaar bij Novartis, ze heeft het dan ook erg naar haar zin als clinical study manager (CSM). Ze werkt op de afdeling Trial Monitoring Operations (TMO), die toezicht houdt op de studies van
60+ dagen geleden - Preview - Opslaan

In-house CRA

Oxfordcorp
of the Client's clinical studies. Exercises independent judgment in planning, organizing, and performing work; monitors performance and reports status to manager . Ensures compliance to the study protocol, domestic and
60+ dagen geleden - Preview - Opslaan

Ontmoet ons team

Novartis
belang dat we niet alleen naar de vergoeding van één middel kijken, maar het grotere plaatje blijven zien.” Meer weten over wat het werk van Ronald zo waardevol maakt? Nine van Zadelhoff Clinical Study Manager “Ik
60+ dagen geleden - Preview - Opslaan

Junior QA Assistant - Project Management

Oxfordcorp - Leiden
required immunological assays. As a QA assistant you will supports one or more project leads in Clinical Immunology with activities relating to coordination of clinical study sample analysis Responsibilities Preparation
FULL_TIME - Preview - Opslaan

Clinical Affairs Manager

Nvvtg.nl - Utrecht
You will be part of the Clinical Team and report to the Head of Clinical Affairs. Your responsibilities Project management; Clinical study management, including database management, writing and reviewing study
FULL_TIME - Opslaan

Lead CRA , Oxford Global Resources

Oxfordcorp
work on the frontline of communication with project stakeholders, ensuring the successful conduct of clinical trials in a variety of therapeutic indications. You will supervise study start-up and site management activities to
60+ dagen geleden - Preview - Opslaan

Opportunities Schmidt Consultancy

Schmidt Consultancy - Zutphen
Through their platform local study startup time of clinical trials is shortened and more patients can easily be included or referred. To ‘fill’ their platform with interesting trials for patients and oncologists, they are searching
FULL_TIME - Opslaan

Regulatory Affairs Administrator

Oxfordcorp
Do you have an education in health-related or scientific discipline and a previous experience in Regulatory Affairs related to clinical trials environment ? Are you also fluent in English with the willingness to work in
60+ dagen geleden - Preview - Opslaan

Country Start-up Specialist

Oxfordcorp
Ensure clinical trial management systems containing all country and site-specific information are maintained and kept current during start up and study maintenance. Manage translations needed for regulatory activities
60+ dagen geleden - Preview - Opslaan

Administrative Assistant

Oxfordcorp
varied job within the context of clinical trials. Function Description The administrative assistant provides support in a wide range of tasks related to the clinical trials run by our pharma client. Responsibilities
60+ dagen geleden - Preview - Opslaan