Ref #: 28189

Employment type: Permanent - Full-Time

Location: Belgium

Posted: 26-May-2021


Key Responsibilities:

* Ensure regional/global clinical operations deliverables progress according to agree upon timelines and milestones as leader of the Study Management Team (SMT). This includes country & site feasibility and site selection, trial set-up, study execution and trial closure and vendor set activities as assigned by the GTL
* Support GTL in leading related CRO country & site activities
* Study Management Team Leader
* Site selection, enrolment, monitor study progress
* Financial planning and tracking
* Document development
* Training and Investigator Meeting
* Cross functional Study Management
* Continuous Quality Focus
* Data Cleaning
* Participate in Global Clinical Development Initiatives as assigned.
* Can act as Subject Matter Expert

Required experience and qualifications:

* BS degree or equivalent required, preferably in Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy)
* Minimum of 6 years clinical trial management experience in the pharmaceutical industry or CRO
* Experience with management and supervision of CROs/vendors is preferred.
* Clinical research operational knowledge, strong project planning/management and effective communication skills
* Languages required : Fluent Dutch & English
* Experience and ability in coordinating global or regional teams in a virtual environment. Proven track record in successfully managing various aspects of trials from start-up to database lock.
* Monitoring experience is recommended or other relevant experience should be considered, such as data management or central monitoring.
* Strong knowledge of standard Microsoft applications, willingness to learn new systems
* Experience with planning tools is an asset
* Willing to travel internationally up to 20% of time

Why this role is right for you:

We offer an exciting and challenging work environment for clinical research professionals looking for an opportunity to contribute to the success of a companies dedicated to researching, developing, manufacturing and marketing pharmaceuticals that improve health and quality of life.

Why join the DOCS team at ICON?

Working at ICON is more than a job, it’s a calling for people who care and are passionate about improving patients’ lives. At ICON, we care about our people and your passion, you are key to our success. We aim to provide an open and friendly work environment where we empower our people and provide them with opportunities to develop their long-term career.
It takes courage to move from one job to another, the process involves careful consideration. Reach out having the conversation that would change your life and the lives of our patients. Our team of recruitment experts will provide the information you need in making the right decision.

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