- Experience Level
- Experienced (non-manager)
A global pharmaceutical organisation now has a requirement for a Senior Clinical Research Associate (SCRA) to work alongside a team of specialists for a groundbreaking trial. The role will be based in their offices and offer 2 days remote working as well.
As a global market leader my client is looking for a Senior Clinical Research Associate (SCRA) with experience of working within multiple phases of Oncology clinical trials and has been actively involved in submitting packages to regulatory authorities and ethical committees.
Essential Skills/Experience: -
Tracking and reporting of essential documents
Vendor Management 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
Degree level education, ideally within Life Sciences / Healthcare
Fluency in English
Strong organisational and communication skills
Ability to work with a wide range of people
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 the Senior Clinical Research Associate (SCRA) feel free to get in touch on 01189 594990. Alternatively, you can email me directly at email@example.com.