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Kiev, UKR JOBS - Covance

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Senior Clinical Research Associate, Ukraine Kiev, UKR

. . . Field? We are proud to have an excellent team of the best professionals on the market and are looking for people who are ready to show true performance and interest in Clinical Trials. Do you like responsibilities and challenges? As a Clinical Research Associate you will lead all aspects of study site monitoring according to Covance SOP, ICH guidelines and GCP. You will take part in pre-study quaRead More

Start Up Associate Project Manager, Ukraine Kiev, UKR

. . .ance with the ownership of country and site budgets * Through continual interaction with local clinical team/s successfully delivers clinical and financial contracts within fair market value * Oversight and tracking of clinical research-related payments * Payment reconciliation at study close-out * Responsible for execution and oversight of clinical trial country submissions and approvals for assiRead More

Manager Clinical Operations, Ukraine Kiev, UKR

. . .vidual Development Plan (IDP), Line of Sight Goals and “Shoves & Tugs” * Responsible for appropriate management and resolution of performance issues * Develop and measure performance indicators for assigned staff * Identify individual training needs and assist with the coordination and conduct of training and development efforts, regionally * Coordinate, conduct, report and follow-up on Quality CoRead More

Senior Clinical Research Associate, Ukraine Kiev, UKR

. . . Field? We are proud to have an excellent team of the best professionals on the market and are looking for people who are ready to show true performance and interest in Clinical Trials. Do you like responsibilities and challenges? As a Clinical Research Associate you will lead all aspects of study site monitoring according to Covance SOP, ICH guidelines and GCP. You will take part in pre-study quaRead More

Manager Regulatory Submissions - Flexible location within EMEA Kiev, UKR

. . .ce tasks. This position is responsible for the management of a team of regulatory professionals and/or responsible for timely preparation/coordination of regulatory submissions for a particular project and must work to high standards (governmental, Sponsor, Covance and self) with minimal supervision. It is the responsibility of this position to ensure that documents are prepared to the required sRead More

Senior Statistical Programmer Kiev, UKR

. . .ch, CRO or pharma company using the SAS programming language * Candidates must be fluent in English language (both verbal and written) Join our growing team and discover your extraordinary potential by working as a Covance Senior Statistical Programmer. As a Lead Statistical Programmer at Covance you will be responsible for all statistical programming deliverables of one or more clinical trials. Read More

Start-up Specialist II, Ukraine Kiev, UKR

. . . regulatory documents for a study and ensuring that the documents meet the specifications required by local regulations, EU Clinical Trial Directive, ICH-GCP, FDA regulations (for IND studies) and/or the study sponsor * Responsible for maintenance of site address and personnel information in the study database as well as maintenance of regulatory documents throughout the duration of the clinical tRead More

Clinical Research Associate II, Ukraine Kiev, UKR

. . . Field? We are proud to have an excellent team of the best professionals on the market and are looking for people who are ready to show true performance and interest in Clinical Trials. Do you like responsibilities and challenges? As a Clinical Research Associate you will lead all aspects of study site monitoring according to Covance SOP, ICH guidelines and GCP. You will take part in pre-study quaRead More

Principal Statistical Programmer Kiev, UKR

. . .using the SAS programming language * Candidates must be fluent in English language (both verbal and written) Join our growing team and discover your extraordinary potential by working as a Covance Principal Statistical Programmer. As a Principal Statistical Programmer at Covance you will be responsible for all statistical programming deliverables of one or more complex clinical trials. You will wRead More

Proj Mgr Drug Safety - Medical Device Kiev, UKR

. . .t Manager and/or Manager of Drug/Device Safety Solutions and Adjudication (DDSS&A). * Monitor and manage the workflow for assigned projects to ensure all deadlines are met and compliant safety reporting in accordance with International reporting regulations, Standard Operating Procedures (SOPS) and safety processing guidelines set forth by departmental management team. * Monitor and manage projectRead More

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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).