Home-Based CRA / Senior CRA Netherlands Upsilon Global are working closely with a small to mid-sized Global CRO, who have recently increased their European presence as they are looking to build a clinical study team of CRAs and Senior CRAs in the Netherlands.
They are operational in a wide range of countries across Europe including the UK, Germany, Italy, The Netherlands and Belgium and are looking to cement their clinical operations within The Netherlands.
This expanding CRO conduct studies in a wide range of therapeutic areas including Oncology and Oncology studies and offer you the opportunity to work on the full cycle of a clinical trial from regulatory submissions and site feasibility, through to study close-out and database lock.
This allows each and every CRA to develop their skills much further than a CRA in a larger CRO, setting you up for Project Management in the future! Background Details confidential, information available upon request.
Specialist mid-sized CRO establishing a presence in The Netherlands and seeking people looking to join them on their development journey.
You’ll be a crucial member of this growing department and the progression opportunities and endless. Main responsibilities Perform all types of site visits including, but not limited to, qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and termination visits.
To identify potential sites for a proposed study in conjunction with the Project Team, and conduct feasibility assessment of sites as required Ensure that all study related communication including e-mail is tracked, printed and filed as required The set-up and coordination of Phase I-IV clinical trials across The Netherlands and Belgium To track patient recruitment by contacting investigators as specified for the study, and discuss potential study risks and opportunities with the Project Manager and LCRA To liaise with all other appropriate departments to ensure the smooth running of the study Mentor and train other CRA’s as and when required Perform document submissions to local authorities To assemble files and ensure documents for the trial master file accurately reflect the progress of the study Other Ad-Hoc CRA duties Education and Qualifications A BSc or BA degree in a lifescience related field Minimum of 4-5 years independent monitoring experience Sound knowledge of ICH / GCP and regulatory requirements Experience using clinical trial management systems Other skills and abilities The ability to communicate effectively in English and Dutch Good computer literacy with working knowledge of PCs, Windows and Microsoft Office Full capabilities to drive in The Netherlands Regulatory experience strongly desired Salary and Benefits Competitive salary Home-based role Great opportunities for career progression Fantastic company culture and cross-functioning teams and departments For further information on this opportunity and to learn of similar positions, please contact Upsilon Global on +44.
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