Bekijk wie IQVIA heeft aangenomen voor deze functie
Beveiligingsverificatie
Vacature opslaan
Welkom terug
Meld u aan om Senior Clinical Research Associate bij IQVIA op te slaan.
Deze vacature melden
IQVIA is a leading global provider of contract research services, advanced analytics and technology solutions to the life sciences industry formed through the merger of IMS Health and Quintiles.
Take your therapeutic expertise to the next level and help drive the evolution of clinical development for a variety of sponsors.
As a Clinical Research Associate within our full-service model, you’ll have the opportunity to embrace your passion for a specific therapeutic area and work with cutting-edge technology developed specifically for CRAs by CRAs.
With access to world-class training and professional development, we’ll give you the tools you need to create the career you want.
Do you want to know more about IQVIA? then see what Forbes said about us!
Essential Functions Of a Clinical Research Associate (CRA)
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Qualifications
Bachelor's Degree or Master's Degree, ideally in scientific discipline or healthcare
Knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines)
Minimum of 12 months of independent monitoring experience
Written and verbal communication skills including excellent command of English and Dutch language
IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential.#CRAFSAJDIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com
Senioriteitsniveau
Niet van toepassing
Soort baan
Fulltime
Functie
Onderzoek, Analist en Informatietechniek
Bedrijfstakken
Geneesmiddelenproductie
Voordrachten verhogen uw kansen op een sollicitatiegesprek met IQVIA 2x
Bekijken wie u kent
Ontvang meldingen over nieuwe vacatures voor Senior partner klinisch onderzoek in Amsterdam.
Meld u aan om vacaturemelding te maken
Vergelijkbare vacatures
Psychodiagnostisch medewerker
Psychodiagnostisch medewerker
Karakter kinder- en jeugdpsychiatrie
Arnhem-Nijmegen Region
(Praktijk)onderzoeksstage E-MST-ID – Den Bosch
(Praktijk)onderzoeksstage E-MST-ID – Den Bosch
de Viersprong, specialist in persoonlijkheid, gedrag en gezin
Den Bosch
Klinisch Psycholoog/Psychotherapeut – Rotterdam
Klinisch Psycholoog/Psychotherapeut – Rotterdam
de Viersprong, specialist in persoonlijkheid, gedrag en gezin
Rotterdam
Onderzoeksmedewerker Alzheimer Centrum Limburg
Onderzoeksmedewerker Alzheimer Centrum Limburg
Universiteit Maastricht
Maastricht
Klinisch Patholoog (0,8 - 1,0 fte)
Klinisch Patholoog (0,8 - 1,0 fte)
Martini Ziekenhuis
Groningen
GZ psycholoog – Goes
GZ psycholoog – Goes
de Viersprong, specialist in persoonlijkheid, gedrag en gezin
Goes
Klinisch psycholoog – Goes
Klinisch psycholoog – Goes
de Viersprong, specialist in persoonlijkheid, gedrag en gezin
Goes
Psychodiagnostisch Medewerker
Psychodiagnostisch Medewerker
GGZ Friesland
Leeuwarden
Systeemtherapeut (i.o.) – Amsterdam
Systeemtherapeut (i.o.) – Amsterdam
de Viersprong, specialist in persoonlijkheid, gedrag en gezin
Amsterdam
Psycholoog in opleiding tot gz-psycholoog (PIOG)
Psycholoog in opleiding tot gz-psycholoog (PIOG)
GGZ Drenthe
Assen
Psychodiagnostisch Werker
Psychodiagnostisch Werker
Treant
Hoogeveen
Klinisch Psycholoog/Psychotherapeut
Klinisch Psycholoog/Psychotherapeut
de Viersprong, specialist in persoonlijkheid, gedrag en gezin
South Holland, Netherlands
Systeemtherapeut (i.o.)
Systeemtherapeut (i.o.)
de Viersprong, specialist in persoonlijkheid, gedrag en gezin
Introduction: My name is Arline Emard IV, I am a cheerful, gorgeous, colorful, joyous, excited, super, inquisitive person who loves writing and wants to share my knowledge and understanding with you.
We notice you're using an ad blocker
Without advertising income, we can't keep making this site awesome for you.
