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Clinical Research Associate - sponsor dedicated - Turkey Istanbul, Turkey

Job Overview Discover new opportunities to grow your career as a Covance FSP Clinical Research Associate. Are you someone with previous regulatory submissions Experience looking for developing your career within this area? At Covance we are recruiting for a CRA/ SCRA to work sponsor dedicated into a top 5 pharmaceutical company to be based based in Turkey. In this role you will be able to be h . . Read More

Site Study Liaison - Sponsor Dedicated Munich, Germany

Job Overview This new and exciting role exists within a Global Healthcare Company. You would be employed permanently by Covance and seconded to the Healthcare Company. The position is home based in Germany and will involve some travel to sites within Germany pretty regularly. Job Title is:- Site Study Liaison / Site Concierge The role is to "support critical clinical development programs" The . . Read More

Clinical Research Assistant, Moscow Moscow, Russian Federation

Job Overview Covance is looking to recruit CTC to join our sponosor in Russia Responsibilities : * Trial and site administration: * Tracking (e.g. essential documents) and reporting (e.g. Safety Reports) * Ensure collation and distribution of study tools and documents o Update clinical trial databases (CTMS) and trackers * Clinical supply & non-clinical supply management, in collaboration with . . Read More

Clinical Study Unit Safety Assistant Brussels, Belgium

Job Overview Join Covance and our FSPx Department! We are actively recruiting a Clinical Study Unit Safety Assistant to join the team of one of our client based in Brussels. As part of this role, you will be involved in Pharmacovigilance and Safety tasks related to clinical studies and programs in humans. This is an exciting opportunity to grow in a dynamic and motivating environment where team . . Read More

In-house CRA, Ukraine Kiev, Ukraine

Job Overview Covance is looking to recruit CTC to join our sponsor in Ukraine Responsibilities : * Trial and site administration: * Tracking (e.g. essential documents) and reporting (e.g. Safety Reports) * Ensure collation and distribution of study tools and documents o Update clinical trial databases (CTMS) and trackers * Clinical supply & non-clinical supply management, in collaboration with . . Read More

   

 

  

Covance Recruiting Process

Below is a general Overview of Our Recruiting Process

If you’d like to work for us, please submit your resume/CV online. If your ability to use or access our electronic application is limited due to a disability, please visit www.gettinghired.com or call 1-800-978-4473 for help.

We consider applications from everyone who is interested in a position with us and who meets the required criteria and qualifications.

If your application is selected, someone from our recruiting team will contact you to arrange an initial screen. We may carry this out over the phone or at a face-to-face meeting. You must complete the screen to be considered for the position.

Based on the results of the initial screen, we may invite you to an interview. One of our recruiting team members will contact you to arrange this. The process may involve several interviews, initially over the phone, and then face-to-face with different members of the hiring team.

Our interviews follow a behavioral-based format. This means we’ll ask you to give us information that’s specific to your professional and educational experiences.

Hiring team members will share and discuss their input and then make their decision.

If you’re the person who best meets the requirements of the position, a member of the hiring team will get in touch to make you an offer of employment. Covance is an eVerify employer (United States only).