Job Description

We are working with this expanding CRO (Contract Research Organisation) to source a Project Co-ordinator/CTA (Clinical Trials Administrator) to join their team.

The job holder will be responsible for providing support to project management. These tasks include setting up and maintaining working project files, project forms and project specific logs. Each project has many specific forms that track items including:

Regulatory documents
INDs
Protocol waivers
SAEs
Enrolment
Data queries
Monitoring visit schedules

Key duties of the role include:

Assembling the Site Study Files and arranging for delivery to the various sites
Tracking supplies at the sites and sending additional supplies
Requesting supplies from various vendors and sending to sites
Ensuring CRAs have adequate supplies and resources
Arranging for documents to be translated
Participating in project team meetings
Assembling and distributing newsletters
Archiving of documents post-study

Qualifications/Skills Required

Candidates should be degree level educated and able to demonstrate proven administration skills.
Candidates should also be based within commuting distance of their offices in Edinburgh, Scotland.