Clinical Trial Coordinator - Brussels

Pharmaceutical Product Development (PPD)

BE-Brussels-Brussels BE St Stevens Woluwe


PPD is currently looking for a Clinical Trial Coordinator to join our clinical team here in Brussels. We will offer you a positive and supportive working environment within one of the most engaged teams in the industry. We will provide you with meaningful and challenging work and the opportunity to acquire valuable personal and professional skills, through our best in class training and development.

The basic purpose of the CTC is to provide technical support to the project team. Will coordinate non-clinical responsibilities of project administration as applicable to the client contract under the direction of the assigned Clinical Manager or Sr. Clinical Manager.Responsibilities include, but are not limited to;Reviews regulatory documents for proper contentPerforms PPD investigator file reviews and logging of outstanding issues in project related tracking toolsLiaises with monitor and investigative sites to resolve outstanding regulatory issues identified Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departmentsAssists with the identification of potential investigators and development/distribution of initial protocol packetsCreates meeting agendas and minutesCoordinates team conference calls and distribution of meeting minutes#LI-NL1

PPD is currently looking for a Clinical Trial Coordinator to join our clinical team here in Brussels. We will offer you a positive and supportive working environment within one of the most engaged teams in the industry. We will provide you with meaningful and challenging work and the opportunity to acquire valuable personal and professional skills, through our best in class training and development.

The basic purpose of the CTC is to provide technical support to the project team. Will coordinate non-clinical responsibilities of project administration as applicable to the client contract under the direction of the assigned Clinical Manager or Sr. Clinical Manager.Responsibilities include, but are not limited to;Reviews regulatory documents for proper contentPerforms PPD investigator file reviews and logging of outstanding issues in project related tracking toolsLiaises with monitor and investigative sites to resolve outstanding regulatory issues identified Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departmentsAssists with the identification of potential investigators and development/distribution of initial protocol packetsCreates meeting agendas and minutesCoordinates team conference calls and distribution of meeting minutes#LI-NL1

Excellent English, French and Dutch language skillsWorking skills across all of the Microsoft packagesAbility to effectively analyse project specific data/systems to ensure accuracy and efficiency Strong interpersonal skills and high attention for detail, with proven ability to handle multiple tasks efficiently and effectivelyGood communication skillsAbility to handle multiple tasks effectivelyExcellent organisational skills will be necessary, along with a self-motivated and positive attitudeSome previous administration experience, preferably within clinical research, although this is not essential.Excellent English, French and Dutch language skillsWorking skills across all of the Microsoft packagesAbility to effectively analyse project specific data/systems to ensure accuracy and efficiency Strong interpersonal skills and high attention for detail, with proven ability to handle multiple tasks efficiently and effectivelyGood communication skillsAbility to handle multiple tasks effectivelyExcellent organisational skills will be necessary, along with a self-motivated and positive attitudeSome previous administration experience, preferably within clinical research, although this is not essential.


2020-07-07 00:00:00


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