Belgium Job Openings
IQVIA
Senior Clinical Research Associate - Belgium (home-based)
FULL TIME
August 15, 2024
Join us in our exciting journey!!
We currently looking for experienced Clinical Research Associates to join our rapidly growing Site Management division team in Belgium.
As an experienced Clinical Research Associate, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a future beyond monitoring with our development opportunities. At IQVIA, you’ll have training and development to plan and progress your career in the direction you choose; we do not believe in a ‘career ceiling.’
This role is working in our core Clinical Site Management function. The team works with multiple sponsors across a multitude of therapy areas and phases, giving you the opportunity to improve and develop your experience. With strategic site relationship managers supporting you throughout your role, this is a fantastic opportunity for you to embed yourself in the wider clinical operations team and work on ground-breaking new medicine development. Our clients are pharmaceutical companies who are dedicated and passionate about improving the lives of patients across several therapeutic areas.
Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
- 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. Escalate quality issues as appropriate.
- 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) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP 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.
- Collaborate and liaise with study team members for project execution support as appropriate.
- Master's Degree in scientific or healthcare discipline.
- Requires at least 2 year of on-site monitoring experience.
- Good knowledge and skilled in the implementation of applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
- Computer skills including proficiency in use of Microsoft Word, Excel and Power Point and use of a laptop computer and i Phone and i Pad (where applicable).
- Written and verbal communication skills including good command of English, Dutch and French languages.
#LI-ANAHDEZ #LI-remote
IQVIA 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
New Job Alerts
Liebherr-Belgium BV
Assistant Finance Manager
Antwerp
PART TIME
November 19, 2024
View Job Description
Beaulieu International Group
Regional Sales Manager BENELUX
Wielsbeke
November 19, 2024
View Job Description
Signify
Sales Support Officer - Export markets (Modular Lighting Instruments)
Roeselare
November 19, 2024
View Job Description
bpost
Senior Leadership Development Expert - Brussels
Brussels
November 19, 2024
View Job Description
FST
Scrum Master ,Customer Servicing and Efficiency: Brussels, Belgium
Brussels
FULL TIME & CONTRACT
November 19, 2024
View Job DescriptionLooking for similar job?
KBR
LCV APS-2 Belgium: Logistics Warehouseman Senior - Contingency
Zutendaal
FULL TIME
August 7, 2024
View Job Description
Deloitte
NSE Employee Relations Leader (Senior Manager), Enabling Functions, UK/Belgium/Netherlands
Zaventem
PART TIME
August 22, 2024
View Job Description
Trusted Advisors
Belgium: Radio Frequency Engineer Roll-Out - Senior -...
Brussels
August 22, 2024
View Job Description
See What’s New: IQVIA Job Opportunities
IQVIA
Business Intelligence Consultant – All rounder
Zaventem
FULL TIME
October 17, 2024
View Job Description
IQVIA
Consultant Analytics Solutions & Strategy
Herent
FULL TIME
October 12, 2024
View Job Description
IQVIA
Pharmaceutical Sales Representative micronutrition in Brussels
FULL TIME
September 13, 2024
View Job Description
New Job Alerts
Liebherr-Belgium BV
Assistant Finance Manager
Antwerp
PART TIME
November 19, 2024
View Job Description
Beaulieu International Group
Regional Sales Manager BENELUX
Wielsbeke
November 19, 2024
View Job Description
Signify
Sales Support Officer - Export markets (Modular Lighting Instruments)
Roeselare
November 19, 2024
View Job Description
bpost
Senior Leadership Development Expert - Brussels
Brussels
November 19, 2024
View Job Description
FST
Scrum Master ,Customer Servicing and Efficiency: Brussels, Belgium
Brussels
FULL TIME & CONTRACT
November 19, 2024
View Job Description