2 x CRA/SCRA - Spain - Madrid and/or Barcelona area - up to €60,000
- Experience Level
- Experienced (non-manager)
CRA/SCRA – Home-based - Barcelona or Madrid area – Regenerative Medicine, Cell & Gene Therapy, Rare Diseases and Oncology
Upsilon Global are currently searching for CRAs/SCRAs in the Barcelona and or/Madrid area. We are looking for 2-3 CRA/SCRAs with at least 3 years independent monitoring experience, preferably having worked with oncology trials and good knowledge of RECIST criteria, however experience within rare diseases, neurology and immunology is also beneficial.
Spain has been identified as a growth region, and this is a position for CRAs that have exceptional relationship skills with sites/PIs and are motivated to develop and grow. As these positions are homebased/remote working, we also need CRAs to be confident, experienced and self-motivated.
If you’re looking for greater responsibility, the opportunity to take protocol ownership from feasibility and start-up all the way through to close-out, we’d love to hear from you. As it’s a small company, attitude and application is everything. Full and comprehensive training will be provided, so even if you’re not fully competent, we’d still love to hear from you!
Details confidential, information available upon request. This is a relatively newly-formed CRO following a merger in 2019 between a small US and small EU CRO. The company has strong financial backing and are now focused on growing and developing their presence in Europe.
- 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 Spain
- 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 3 years independent monitoring experience
- Oncology experience preferred
- 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 Spanish
- Good computer literacy with working knowledge of PCs, Windows and Microsoft Office
- Full Spanish driving licence
For further information on this opportunity and to learn of similar positions, please contact Upsilon Global on +44. (0). 20. 3. 87. 5. 99. 66. or email ‘applications (at) upsilonglobal . com’
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