Senior Clinical Research Associate - home-based, UK

Pharm Research Associates Limited ,
London, Greater London
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Overview

Summary: Providing innovative solutions for our clients is what we do. But innovation just for the sake of innovation isn’t why we do it. Side-by-side with our clients, we strive to move drug discovery forward, to help them develop life-saving and life-improving drugs. We help change people’s lives for the better every single day. It’s who we are. And it’s who you could be too.Working fully embedded within one of our pharmaceutical clients, with the support of PRA right behind you, you’ll be at the heart of our client’s innovation. Job Description: As a Clinical Research Associate, you will be dedicated to one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies and vaccines for many of the world’s most challenging diseases. Be ready to work in an environment driven by quality, innovation and continuous improvement. Operating within an established monitoring model, your key responsibilities are: Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out according to sponsor SOP’s. Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan. Developing effective relationships with investigator site staff to ensure that key clinical metrics are met. Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues. You are: Passionate, innovative and committed. Here at PRA we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have: Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment. A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential. You will be educated to degree level in a life science discipline or be a licensed healthcare professional. Experience working on Oncology trials or complex studies would be an advantage for this role. Home based position This position will pay a salary fully commensurate both with the significance of this appointment and with the required caliber of the successful candidate. Your health, your family, your career, your money — the things that matter to you, matter to us. The benefits of PRA just get better and better. PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace. This job was originally posted as www.totaljobs.com/job/89747584

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