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.