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 48 countries and more than 21,000 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 and optimize value in delivering life-changing therapies to improve health.
Would you like to become part of our Site Intelligence and Activation (SIA) group in PPD, Turkey? Then we have an opportunity for you - join our team of global professionals as Country Approval Specialist The Country Approval Specialist will be responsible for obtaining Ethics and Regulatory approvals to conduct clinical studies in Turkey and to ensure the activation of the sites in clinical studies.
Main duties and Responsibilities include but are not limited to :
Ideally candidates will have minimum 1-2 years of regulatory and submission experience or CRA experience in clinical studies and good knowledge of all applicable national regulatory requirements.
Contracts experience will be considered as an advantage. If you have excellent English skills and ability to work in a team environment and independently with minimum supervision then apply now!
What we offer :
HOW TO APPLY : Please submit your CV in English. Suitable candidates will be contacted accordingly.
PPD is an equal opportunity employer.