Ref #: 28015

Employment type: Permanent - Full-Time

Location: Belgium

Posted: 16-Mar-2021

Description

Key responsibilities:

* Participates in site feasibility and/or pre-trial site assessment visits, providing recommendation from local area about site/investigator selection in collaboration with the trial team
* Acts as primary local company contact for assigned sites for specific trials
* Attends/participates in investigator meetings as needed
* Responsible for executing activities within site initiation and start-up, site monitoring, site management and site/study close-out according to internal SOPs/WIs/IFUs and policies
* Ensures site staff is trained and the corresponding training records are complete and accurate at any time point during all trial phases
* Contributes to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target
* Ensures site study supplies (such as Non-IP, lab kits, etc.) are adequate for trial conduct
* Ensures that all AEs/SAEs/PQCs are reported within the required reporting timelines and documented as appropriate. For AEs/SAEs, ensures that they are consistent with all data collected and with the information in the source documents
* Maintains complete, accurate and timely data and essential documents in systems utilized for trial management (e.g. CTMS, eTMF/IF, Trial Master Source and SharePoint)
* May be assigned as a coach and mentor to a less experienced site manager
* May contribute to process improvement and training
* Leads and/or participates in special initiatives as assigned
* May assume additional responsibilities or special initiatives such as "Champion" or "Therapeutic Area Expert"


Required experience and qualifications:

* A minimum of a BA/BS degree is required. A degree in a health or science related field is preferred
* A minimum of 2 years of clinical trial monitoring experience is preferred
* Must have experience in Clinical Research or equivalent qualification
* Specific therapeutic area experience may be required depending on the position
* Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines
* Strong IT skills in appropriate software and company systems
* Willingness to travel with occasional overnight stay away from home
* Proficient in speaking and writing in Dutch and English (French a strong plus)
* Good written and oral communication skills


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.
At ICON you will have the opportunity to work with one of the global top 20 pharmaceutical companies, working on novel therapies that deliver real impact. If you want a career with a difference, ICON is the place for you.


#CRAjob