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JOB DETAILS
Position Clinical Research Associate (CRA) - Ukraine- Home Based
Company Confidential
Location Home Base
Country Ukraine
Job Description Clinical Research Associate (CRA) - Ukraine

My client is a leading CRO they seeking high caliber Clinical Research Associates to work at an international level on trial within the Inflammatory therapeutic area. There are 8 sites in Ukraine (an average of 10 patients per site) which were participating in a previous study and are willing to continue to this one (anther phase 2 study). The study will be 3 months per patient.

Key Duties and Responsibilities:

* EC and RA submissions

* Contribute to study documents e.g. ICF and adjust to local requirements

* Manage and monitor sites from initiation visit to close-out. Ensure sites comply with protocol, Good Clinical Practice and any other relevant guidelines.

* Manage clinical documentation including the TMF. Review trial data including CRF. Provide input to regulatory and ethical submissions.

* Work with Drug Safety in the case of SAEs and AEs

* Maintain a close working relationship with the Clinical Trial Manager.

* Negotiate contracts and payment with the study site Investigators.

* Manage drug supplies.

Education and Skills:

* Appropriate qualification in Life Sciences, Nursing or Medical Degree.


* Working knowledge as a Clinical Research Associate (CRA) ESSENTIAL Candidates will be proficient in monitoring multi-site trials.

International experience is highly desirable.

* Fluent in English


My client offers a competitive salary and comprehensive benefits package. For immediate consideration, please email your CV with salary requirements.


Company Profile Confidential
Job Type Full Time
Salary Upto 0  €   Per Month
Skills Required ICH-GCP is a must RA, EMEA/FDA regualtory submtions
Reference CRAHBUKRAINE
Posted On 23 December 2009
Last Date to Apply 10 January 2010
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