Local Delivery Lead - CRO
Description
Job Details
Upsilon Global are partnering with a Global CRO partner to present exciting opportunities across LATAM as they continue to expand worldwide!
Partnering with large Sponsor and Biotech collaborators to present complex studies in Rare Disease, Dermatology and Oncology, our CRO partner are excited to extend their team into new areas of research.
If you are an experienced CSA who is looking to join a familiar, established CRO, and keen to drive their development across LATAM, then please apply!
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.
Assist with document submissions to local authorities Ensure that all study related communication including e-mail is tracked, printed and filed as required 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 Other Ad-Hoc CRA duties
Education and Qualifications
- Lifesciences related degree (BSc / MSc / PhD) Previous experience as a clinical research associate Sound knowledge of ICH / GCP and regulatory requirements Experience using clinical trial management systems
- Other skills and abilities Experience working in Study Start-Up is essential Experience working in Oncology, Dermatology, Rare Disease is beneficial Experience in Regulatory Affairs is beneficial, but not essential Good computer literacy with working knowledge of PCs, Windows and Microsoft Office