Site Activation Coordinator - Brussels, België - Novasyte

Novasyte

Geverifieerd bedrijf

Brussels, België

3 weken geleden

Geplaatst door:

Sophie Dubois

beBee Recruiter

Beschrijving

Join us in our amazing journey

Fantastic opportunity to embed yourself in our global clinical operations team working as Site Activation Coordinator where you are going to be in charge of manage and lead activities associated with
_Feasibility and/or Site Identification for regional and/or country projects and/or programs._

Your responsibilities might include_
Under general supervision, perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.
Prepare site documents, reviewing for completeness and accuracy. nform team members of completion of regulatory contractual. and other documents for individual sites._
Distribute completed documents to sites and internal project team members._
Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information._
Review, track and follow up the progress, the approval and execution of required documents such as questionaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.

Qualifications and Profile- Bachelor's Degree Life science or related field- With 1-2 years of experience in clinical trials.- Dutch & French and English Proficient level- Effective communication, organizational, and interpersonal skills.- Ability to work independently and to effectively prioritize tasks.- Ability to manage multiple projects. Knowledge of applicable regulatory requirements, including local regulations, SOPs and company's Corporate Standards.- Understanding of regulated clinical trial environment and knowledge of drug development process.- Ability to establish and maintain effective working relationships with coworkers, managers and clients.

IQVIA is an equal opportunity employer. We make employment decisions based on qualifications and merit. We prohibit discrimination based on any unlawful consideration such as age, race, national origin, gender or other "protected status."

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and whatever your career goals, we are here to ensure you get there

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

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