Data Manager/Senior Data Manager - 2373628 career at Valesta in Northern

Valesta is in need of Data Manager/Senior Data Manager - 2373628 on Sat, 28 Jul 2012 18:03:55 GMT. Data Manager/Senior Data Manager Incumbent will provide timely and professional ongoing management of clinical trial data, Phases I to IV, by preparing validation plans and chairing validation meetings. In addition, you will prepare material for and presenting at Investigator meetings, identify errors and inconsistencies in CRF data and ensure their resolution, and perform serious adverse event...

Data Manager/Senior Data Manager - 2373628

Location: Northern New Jersey

Description: Valesta is in need of Data Manager/Senior Data Manager - 2373628 right now, this career will be placed in New Jersey. Detailed specification about this career opportunity kindly read the description below. Data Manager/Senior Data Manager Incumbent will provide timely and professional ongoing management of clinical trial data, Phases I to IV, by preparing validation plans and chairing validation meetings. In addition, you will prepare material for and presenting at Investigator meetings, identify errors and inconsistencies in CRF data and ensure their resolution, and perform serious adverse event and external data reconciliation e.g., lab data, in order that databases can be declared clean and locked according to strict quality standards. You will also represent the DM function in International clinical teams, to define project as well as trial level data management strategy and manage clinical trials or projects. Qualifications include: A degree in life sciences, pharmacy, nursing (e.g., SRN in UK) or equivalent relevant experience; typically 2 or more years experience in drug development, including 1 or more years in the discipline of data management; good understanding of clinical trial methodology, GCP and medical terminology; good computer skills; attention to detail; good organizational and project management skills; good interpersonal and communication skills and the ability to operate effectively in an international environment; good understanding of physiology, pharmacology, clinical study objectives and the drug development process; good problem solving skills; good presentation skills; the ability to work as part of a team and without close supervision; and the ability to work under pressure and meet timelines. Fluent in written and spoken English, knowledge of a second language is an advantage.
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If you were eligible to this career, please email us your resume, with salary requirements and a resume to Valesta.

If you interested on this career just click on the Apply button, you will be redirected to the official website

This career starts available on: Sat, 28 Jul 2012 18:03:55 GMT



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