Clinical Research Associate / Homebased / England

Clinical Research Associate / CRAs – all levels - h ome-based Do you have clinical trial monitoring of UK-based based clinical studies gained within a CRO or pharmaceutical company? Are you willing to drive to sites 2 to 3 times per week UK-wide or regionally? Have you performed all aspects of CRA duties? We are looking for motivated, reliable and dedicated CRAs who can demonstrate at least 12/18 month independent external site monitoring of commercial studies (or a mix of commercial clinical studies). Oncology and other complex therapeutic areas are also of interest, especially if gained on phase III commercial trials. What is Offered As a field-based/home-based CRA / Clinical Research Associate, you will have the opportunity to work with a sought-after client’s clinical trials in phase I-IV across different therapeutic areas. Our client is looking to recruit motivated and dedicated CRAs at all levels (Clinical Research Associate) in various UK regions (South West, West Midlands, South M4 corridor, Midlands, and/or Greater London areat). 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 23 days annual leave plus UK bank holidays, car allowance, pension, medical health insurance, etc. Regionalized monitoring Fully structured 4-week training for all new starters The Role and your Responsibilities The experienced field based / home based CRA (Clinical Research Associate) will perform 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; • Implement new technologies and systems at clinical sites, e.g. EDC systems; • Ensure appropriate safety reporting as well as tracking and reporting of adverse events (AEs and SAEs) and to verify case reports and source documentation; • Input and maintain electronic site management systems, provide input into clinical monitoring plans, input into case report forms and study-related documents as requested. What is Required Degree (BA/BS/BSc) in life sciences or qualified nurse Previous CRA experience with external/independent clinical trial monitoring experience gained in the UK within the clinical research industry (Pharma, CRO or biotech) Willingness to travel 50-60% of the time to monitor sites by car Full-time availability Full clean driving licence Able to work effectively within fast-paced working environments Full UK working eligibility Start date negotiable for the right candidate Please send your CV today to find out more details. Applicants who have not had a response within two weeks should assume their application has been unsuccessful. This job was originally posted as www.totaljobs.com/job/89855698