£20k - £24k
Our large pharmaceutical client is looking for an experienced CTA to join their team and provide vital support to their team.
The Role and your Responsibilities
You will provide initial support to the Local Trial Manager by distributing and tracking investigator feasibility questionnaires. Upon selection of investigator sites, you will be responsible for the collection and review of regulatory documents for accuracy and completeness at study start up as well as throughout the study
What is Required
- Distributes feasibility questionnaires to investigators being considered for study participation, tracks and summarizes results
- Distributes final documents (investigator list, IB, protocol, ICF template, FDF) to sites
- Initiates and tracks confidentiality agreements with sites
- Initiates and maintains investigator and site contact information
- Reviews documents received from sites for accuracy and completeness, ensures that they comply with SOP's and regulations
- Bachelor's degree or equivalent
- 1-2 years of pharmaceutical industry experience as a CTA
- Understanding of Good Clinical Practices and knowledge of regulatory requirements preferred
- Good interpersonal skills and teamwork
- Ability to prioritise and manage multiple tasks
What is Offered
Salary ranging from £20,000 to £24,000 per annum depending on level of experience
Permanent contract with competitive package & great benefits, seconded to our client on a 12-month renewable contract basis
Company perks include: competitive basic annual salary, pension, medical health insurance
Further details & applications
To find out more about this vacancy, or to apply, please contact
Elisabeth.Knighton@docs-int.com (
01273 735827).
