As a field-based CRA (Clinical Research Associate), you will work within a department (approx 30 staff) that carries out and coordinates clinical trials in Europe. As a CRA, you will ensure the implementation and monitoring according to international (FDA/ICH GCP) guidelines and company SOPs of clinical research & development trials in Europe.
You will perform full CRA duties from trial (pre-) initiation phase, to clinical monitoring activities related to the ongoing of the trial such as visiting the investigational site(s) and meet with investigators and staff involved in a trial; to preparing and performing close-out visit ensuring all files (ISF and TMF) are up to date, all outstanding action items are resolved, all data is clean, all follow-up SAEs information is collected, drug accountability is correct and remaining drug (used/unused) is returned or destroyed.
What is required
- University degree in medicine, science or equivalent,
- Previous UK-based clinical monitoring experience;
- Excellent communication and IT skills;
- Ability to work to tight deadlines within a pressurised environment ;
- Excellent interpersonal skills enabling you to deal with any queries in a timely manner;
- Ability to travel UK-wide (and sometimes in Europe);
- Have full current UK work eligibility;
- Have a clean valid UK driving licence
What is offered:
- Salary ranging from £28,000 to £32,000 per year depending on level of experience.
- Permanent contract with competitive package, seconded to our client on a 12-month renewable contract basis
- Company perks include: car allowance, pension, medical health insurance, etc.
Further details & applications
To find out more about this vacancy, or to apply, please contact
Elisabeth.Knighton@docs-int.com (
01273 735827).
