Ref #: 28910

Employment type: Permanent - Full-Time

Location: England

Posted: 10-May-2021

Description

Our client is looking to recruit motivated and dedicated CRAs at all levels (Clinical Research Associate) in various regions of the UK.


You will be an experienced field based / home based CRA (Clinical Research Associate) with a good track-record in all aspects of CRA work covering site evaluation, site initiation visits, site monitoring and close-out visits across phase II and phase III clinical trials in different medical indications.

CRA responsibilities:
* Facilitate subject enrolment at the site level with focused patient recruitment strategies and action plans;
* Identify site needs and site-related issues, escalate and/or initiate corrective actions when necessary, providing solutions for site staff to facilitate the clinical trial process;
* Respond to site-related queries and escalate site-related issues with operational site management responsibility;
* Perform investigational product accountability and reconciliation, maintain site study supplies, and facilitate the resolution of clinical queries to investigative staff;
* Build and maintain solid and long-term professional relationships with investigators and site staff;
* Ensure clinical study sites are conducting clinical trials in compliance with the respective protocol, our client's SOPs and applicable ICH/GCP guidelines and regulations;
Assist in preparing sites for audits, review audit reports and contribute to resolving findings;


What is Offered
As a field-based/home-based CRA II or Senior CRA, you will have the opportunity to work with a super Biotech on a variety of exciting clinical trials.
* Permanent and full-time contract of employment seconded to our client
* Home-based working
* Salary according to actual level of skills and experience
* Company benefits to include generous annual leave plus bank holidays etc
* Fully structured 4-week training for all new starters

What is Required
* Previous CRA experience of commercial phase II and phase III studies
* Proven external/independent clinical trial monitoring experience gained in the country
* Life science degree (BSc) or RN (registered nursing qualification)
* Able to drive to sites in in the UK 2 times or 3 times per week
* Full UK working eligibility
* Ability to work effectively within fast-paced working environments
•* Full clean driving licence
* Start date asap / immediate preferred (negotiable for the right candidate)

For more detail and to apply, please email me at: Elisabeth.Knighton@DOCSGlobal.com

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