CLINICAL RESEARCH ASSOCIATE (CRA) - United Kingdom

Expiring today

Recruiter
PRA Health Sciences
Location
All Saints
Posted
23 Jan 2018
Closes
18 Feb 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
CLINICAL RESEARCH ASSOCIATE (CRA) Location: Home-based, United Kingdom 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. Responsibilities: Working within one of PRA’s client-dedicated programs you will be fully-aligned to one Sponsor, performing your role in accordance with their clinical SOP’s, with access to their internal systems and technology platforms. The Sponsor is a major global pharmaceutical company with a leading portfolio of medicines and vaccines used for Oncology, Neuroscience, Cardiovascular and Infectious Diseases. Operating within an establised regionalised 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. Desired skills and qualifications: The successful candidate for this role will be able to demonstrate prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment. Prior working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential. Fluency in English language is an absolute requirement, as well as an ability to communicate effectively with others and manage your time effectively. 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. If you have any questions please email recruiteruk@prahs.com or call our recruitment department at +44 (0) 1189 213 652

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