Location: Europe, Middle East & Africa-Poland-Mazowieckie-Wa
Closing Date: 26 Mar 17
Type: Full Time
Salary (£): On Application
Pharmaceutical Product Development, LLC (PPD) has been named Best contract research organization (CRO) in the Triangle Business Journal’s 2016 Life Sciences Awards. 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. ...
Pharmaceutical Product Development, LLC (PPD) has been named Best contract research organization (CRO) in the Triangle Business Journal’s 2016 Life Sciences Awards. 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 16,000 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. PPD has an exciting opportunity for a CRA to join us and work exclusively for one of our strategic pharmaceutical partners in Poland. As part of the PPD services to this partner, you will be dedicated to client-specific projects and sites, collaborating with the clients teams under some of their systems and processes. Senior / Clinical Research Associate (Client onsite), Poland This is a great opportunity for CRAs at any level currently working within the life science sector for pharmaceutical companies, biotech companies or CROs who would enjoy the opportunity to work for one client. 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. *LI-IG1
QualificationsEducation and Experience: • University degree in a science related field. • At least 1 year independent monitoring experience in clinical development phase II-IV. • Understanding of ICH-GCP, EU and FDA requirements • Fluency in English and in Polish • Valid Driver's License where applicable • Proven clinical monitoring skills • Demonstrated understanding of medical/therapeutic area knowledge and medical terminology • Demonstrated ability to attain and maintain a working knowledge of Good Clinical Practices and applicable Standard Operating Procedures • Good oral and written communication skills, with the ability to communicate effectively with medical personnel • Good organizational and time management skills • Ability to work in a team or independently as required • Good computer skills: good knowledge of Microsoft Office and the ability to learn appropriate software Our offer: 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. Please submit your CV in English. Registration on our website will also give you the opportunity to be considered for other positions if this one is not the most appropriate for your qualifications and experience. Only short-listed candidates will be contacted. PPD is an equal opportunities employer.
|Tel:||+44 1223 374100|
|Website:||Visit Our Web Site|
PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.