MSI Pharma is currently hiring a Genomics Initiative Clinical Study Advisor for one of our long-term UK Pharmaceutical clients to support their Centre for Genomics Research (CGR) and to work on a remote basis.
As a Clinical Study Advisor, you would:
- Play an integral part in ensuring that clinical study teams include all documentation required to support the compliant collection of genomic samples and subsequent data generation.
- Work closely with P&O's Genomics Clinical Science Adviser to learn about country and site level requirements that may inhibit collection of this sample.
- Manage a busy query management system, fielding questions direct from study teams and other key stakeholders. - Be responsible for using internal systems to survey which clinical studies are being set up and are eligible to collect the genomic sample.
- Review clinical study supporting ethics and protocol documentation to ensure the genomic sample is consistently and compliantly represented.
If you are interested in applying, please reach out to Yuan Xie via
Looking forward to hearing from you soon!