Clinical Research Associate (CRA) 45,000 Car Allowance Regional Monitoring A global CRO now has a requirement for a Clinical Research Associate (CRA) to work alongside a team of specialists for a ground-breaking trial.
If you’re considering sending an application, make sure to hit the apply button below after reading through the entire description.
The role will be home based and require travelling to sites regionally.
The successful Clinical Research Associate (CRA) will have experience of working within multiple phases and have experience submitting packages to regulatory authorities and ethical committees.
- Tracking and reporting of essential documents 2 years Independent Monitoring experience Updating clinical trial systems and databases (CTMS) Collating, archiving, and distributing study documents (TMF) Updating study materials (e.g.
Patient diaries, instructions) Organising and supporting meetings, including investigator meetings Life Sciences / Healthcare Degree Strong organisational and communication skills Ability to work in a cross functional team Desired Skills/Experience:
- Updating investigator lists for site evaluation and start up activities Preparing packages for submissions to Regulatory authorities and Ethical committees Working closely with finance teams for tracking and reporting of budget negotiations, contract development and management of investigator and site payments If you feel as though you, or someone you know, would be suitable for the position of a Clinical Research Associate (CRA) feel free to get in touch on 01189 594990.