Senior clinical research associate field based, uk
- 1. Providing Flexible Resourcing Solutions CTC Resourcing Solutions, founded in Basel, Switzerland in 1997, is a specialist staffing organisation based in Basel, London and Munich, providing flexible resourcing solutions to the pharmaceutical industry across Europe, with contract and permanent placements in clinical development, data management, statistics, regulatory affairs and medical marketing. For one of our clients, we are currently looking for a Senior Clinical Research Associate Reference Number: 50-13-823-SCRA-W Type of placement: Permanent Location: Field Based (UK) Our client is the word’s leading provider of biopharmaceutical services. With a network of > 27,000 professionals working in over 80 countries, it has helped develop or commercialise all of the top 50 best selling drugs on the market. Through its application of extensive therapeutic, scientific and analytical expertise, our client helps biopharmaceutical and health sciences customers navigate the increasingly complex landscape with more predictability to enable better outcomes. Main Responsibilities:  Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.  Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.  Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage on-going project expectations and issues.  Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Team Lead (CTL) and/or line manager.  Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, Case Report Form (CRF) completion and submission, and data query generation and resolution.  Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation.  May provide assistance to more less experienced clinical staff. Qualifications and Experience:  Degree, in a scientific or healthcare discipline  Solid prior monitoring experience, preferably two years Our offer:  Competitive basic salary  Company Car  Bonus Should you be interested in the above position and wish to apply, please send your application with your CV, quoting the above reference number, to our recruitment team at recruitment@ctcon.ch CTC Clinical Trial Consulting, Studio F7, 80 Silverthorne Road, SW8 3HE London, UK Tel.: +44 207 193 9972 www.ctcon.ch info@ctcon.ch
- 2. Flexible benefits package including, but not limited to: ï‚· Contributory Pension ï‚· Private Health Insurance ï‚· Permanent Health Insurance ï‚· Life Assurance ï‚· Additional benefits based on health and well-being ï‚· 25 days holiday increasing with length of service Should you be interested in the above position and wish to apply, please send your application with your CV, quoting the above reference number, to our recruitment team at recruitment@ctcon.ch CTC Clinical Trial Consulting, Studio F7, 80 Silverthorne Road, SW8 3HE London, UK Tel.: +44 207 193 9972 www.ctcon.ch info@ctcon.ch