Senior/Clinical Research Associate (Home-based Barcelona)-121279
Nr ref.: /JOBS.pl
PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 46 countries and more than 15,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help clients and partners bend the cost and time curve of drug development to deliver life-changing therapies that improve health. For more information, visit .
PPD are looking for experienced Clinical Research Associate's who are interested to join our team of Home Based CRA's in Barcelona. Due to increasing client needs within the Catalonia region we are continuing to network with the best and the brightest in the industry.
PPD is one of the world's largest 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.
Our sustained year on year growth means that we are looking for exceptional clinical talent to join our team.
You should thrive in multi-national project teams and be focused on delivering exemplary levels of customer service on multiple, challenging projects. 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.
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 and challenging work and the opportunity to acquire valuable personal and professional skills; through our best in class training and development. QualificationsA minimum of 2 years on site monitoring experience University degree in a science related field or are a certified health professional
In depth knowledge of ICH-GCP, EU and FDA requirements
Experience of clinical trials in Spain
Willingness and ability to travel
Excellent English and Spanish skills
Previous experience in the CRO industry would be advantageous *LI-EC1