Join a dynamic environment where your expertise as a Clinical Study Administrator will directly contribute to impactful clinical research projects. This role offers a unique opportunity to support clinical study staff and foster valuable collaborations within the Clinical R&D organization.
As an ideal candidate, you are an adept Clinical Study Administrator who thrives on attention to detail and possesses strong organizational capabilities. You are looking to leverage your clinical administration skills in a role that emphasizes both independence and teamwork.
You manage the timely tracking and filing of essential study documents, ensuring the completeness of the Trial Master File.
You assist study staff and investigators in resolving issues related to study files efficiently.
You support project managers in administrative tasks related to assigned clinical studies.
You maintain and track relevant activities within the clinical trial management system.
You provide logistical support for Investigator meetings and assist in the distribution of safety documentation.
You participate in process improvement activities for CTMS/vTMF within the department.
You may assist with additional administrative support as assigned by supervisors or study leaders.
What are we looking for?
You hold a Bachelor's degree.
You have at least 1 year of administrative support experience, preferably in a clinical context.
You possess proficiency in Microsoft Office, including Excel and PowerPoint.
You exhibit strong attention to detail and organizational skills.
You have excellent written and verbal communication abilities.
You are based in Belgium.
You are fluent in English (spoken and written); proficiency in any other European language is an advantage.
Show more Show less