- CRA / Clinical Research Associate - Kiev, Ukraine
CRA / Clinical Research AssociateKiev, UkraineOffice-basedPermanent inVentiv Health -Transforming Promising Ideas into Commercial Reality Job description inVentiv Health Clinical are currently recruiting for a dedicated and motivated CRA with previous clinical research experience in Ukraine to work office-based as a Clinical Research Associate within our global pharma client. ...
- Contract Management Specialist - Kiev
Contract Management Specialist Office-based in Kiev, Ukraine Full-time (1 FTE) Permanent (salary and benefits) Job description inVentiv Health Clinical are currently recruiting for a dedicated and motivated Contract Management Specialist to work with our global Pharma client in Ukraine. Based in their offices in Kiev you will be working with the Site Management & Monitoring team in Ukraine, Poland and Baltic countries aligned to the Strategic Study Start Up team. ...
- Site Monitor / Clinical Research Associate / CRA, office-based, Kiev, Ukraine
DOCS has partnered with a highly prestigious organisation with one of the most robust pipeline within the industry. We have a great job opportunity for a CRA / Clinical Research Associates with experience in independent on-site monitoring that is ready to further develop their career and enjoy working for a global organisation in their offices in Kiev.
- CLINICAL RESEARCH ASSOCIATE (CRA) - Ukraine
An outstanding opportunity to join one of the world’s leading contract research organisations and be part of a dynamic and growing international company. Join PRA Health Sciences as a Clinical Research Associate (CRA) and help realize your career potential.
- Clinical Research Associate II/Sr CRA, Ukraine
inVentiv Health – Transforming Promising Ideas into Commercial RealityJob Title:Clinical Research Associate II/Sr CRA, UkrainePrimary Function:As a Clinical Research Associate you will be at the forefront of the clinical trials practice. As a member of our Clinical Research Team you will reflect its unique characteristics and help world class companies to ensure the right size and custom fit for their trial needs. ...
- Country Approval Specialist, Ukraine-136761
Would you like to become part of our Site Intelligence and Activation (SIA) group in PPD? Then we have an opportunity for you - join our team of global professionals as Country Approval SpecialistThe Country Approval Specialist will be responsible for obtaining Ethics and Regulatory approvals to conduct clinical studies in Ukraine and to ensure the activation of the sites in clinical studies. ...
- Country Submission Specialist II, Ukraine
inVentiv Health -Transforming Promising Ideas into Commercial RealityJob Title: Country Submission Specialist II, UkrainePrimary Function:A local specialist regarding regulatory Institutional Review Board (IRB) and Ethics Committee (ED) processes and documentation requirements for the start-up and conduct of clinical trials according to Good Clinical Practice and local regulations. A Study Start Up Specialist may be assigned to more than one project. ...
- Snr Clinical Project Manager – International CRO - Ukraine
International CRO is looking for an experienced Clinical Project Manager. It is a renowned CRO that has expanded trully globally over the last 20 years on the market and been present in Ukraine for the last 10 years. Our client has a stable position on the market and is continuously growing and expanding its clinical operations market presence. Benefits: Generous annual salary + medical insurance for you and your family+ company car + annual sports card + many other benefits Snr. ...
- COVANCE UKRAINE is currently seeking to hire a Clinical Start-Up Specialist
We are recruiting for our Global Site Services (GSS) team in Kiev, Ukraine and are currently seeking to hire a Clinical Start-Up Specialist to help support the team with contacting sites, collecting documents and providing critical data. This is a permanent, full time position, based in our Kiev office.
- Head of Regulatory Affairs - Italy - OTC role - ROME - Must have local market submissions experience
To apply for the for this regulatory affairs role please call Julie Cooper on 07951 082482 or send your CV to: