CRA, Field-Based
£28k - £32k
Would you like to join one of the most respected global CROs and develop your clinical career? We are looking for a candidate who will contribute to the team spirit and is ready to take on a new challenge
The Role and your Responsibilities
Working within a highly qualified team you will identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV ensuring that applicable regulations and principles of ICG-GCP are adhered to
What is Required
- With a University degree in medicine, science or equivalent, you will have previous monitoring experience in medium sized studies or international studies to undertake the relevant tasks of this role and knowledge of ICH GCP guidelines (for all roles above entry level)
- Experience in independent monitoring (minimum of 1.5 years), and at least 1 year of experience working within Oncology, Endocrinology or CNS
- Excellent written and verbal communication skills
- Computer literate with Microsoft Office
- Ability to produce accurate work to tight deadlines within a pressurized environment
- Excellent interpersonal skills will be essential to enable you to deal with any queries in a timely manner
Why this Vacancy is right for you
If you like challenges and dynamic quality focused environment, this position is for you. Working on diverse projects and gaining experience across several therapeutic areas will help you to make a step up in your career. Take the pride in joining the team. Package includes: £28-£32k, field based, competitive benefits package.
Further details & applications
To find out more about this vacancy, or to apply, please contact
Elisabeth.Knighton@docs-int.com (
01273 735827).
