As a CRA Trainee, you will have the chance to start your career within clinical research, while being engaged in the company’s training program. You will gain knowledge and skills to conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements independently.
In our Global Functional Resourcing model (GFR) we work in a close partnership with our key customers in order to deliver a comprehensive clinical trial management. Within this team, you will focus on different projects of one single pharma client in Belgium and gain direct and in-depth experience of working with this sponsor.
Your trainings period and your typical responsibilities might include:
Complete appropriate therapeutic, protocol and clinical research training
Gain experience in study procedures by working with experienced clinical staff
Under close supervision, perform site selection (if applicable), initiation, monitoring and close out visits in accordance with contracted scope of work and good clinical practices
If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas to CRA for improving site recruitment plan and assist in tracking progress
Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues
Under close supervision, 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
You should have:
A Bachelor's or higher level degree, preferred in health care or other scientific discipline; or equivalent combination of education, training and experience
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer
Previous experience in clinical study conduct activities is a pre
Fluent written and verbal communication skills in Dutch and French including good command of English language
Good organizational and problem-solving skills and effective time management skills
If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team.
Connect to great opportunity.
At IQVIA, 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. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.