Clinical Research Associate (CRA)

Negotiable DOE
24 Aug 2016
20 Oct 2016
Contract Type
PPD has an exciting opportunity for a pharmaceutical dedicated home or office based Senior or Clinical Research Associate to join us exclusively for one of our strategic pharmaceutical partners. PPD works in close collaboration with this partner; you will be dedicated to the client projects in Southern England the possibility of sites outside of this region. You will work within their teams, systems and processes on behalf of PPD. This is a great opportunity for a CRA's with experience currently working within the life science sector for pharmaceutical companies, Biotech companies or with other CRO's. As the trusted partner of some of the most innovative big pharma and biotech companies; our CRA's have the opportunity to work on challenging projects across a wide range of therapy areas. Our vision is to be the global leader in our industry; based on consistent quality and execution, exceptional customer-aligned service and constant innovation. You should thrive in project teams and be focused on delivering exemplary levels of customer service. You will have excellent communication and interpersonal skills and are looking to work in a collegiate environment where you want to take true ownership for your work. You will perform and coordinate all aspects of the clinical monitoring process. You shall also be qualified to conduct monitoring activities independently. In return we will offer you a positive and supportive working environment within one of the most engaged teams in the industry; who are truly recognised as the cornerstone of our success. We will provide you with meaningful work and the opportunity to acquire valuable personal and professional skills. PPD is a leading global contract research organization providing drug discovery, development, lifecycle management, laboratory services and outsourcing solutions. With offices in 46 countries and more than 15000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a commitment to quality to help clients and partners accelerate the delivery of safe, effective therapeutics to patients and maximize returns on their R&D investments. The successful candidate will be primarily tasked to set up and monitor clinical trials conducted as part of international projects.