Sr. Data Manager (Ascot)
Location: Kingdom New York
Description: Pharm-Olam International is looking of Sr. Data Manager (Ascot) right now, this vacancy will be placed in New York. More details about this vacancy opportunity kindly see the descriptions. Pharm-Olam International seeks a Clinical Data Manager with 2+ years experience of data management in pharmaceutical industry. This is an in-house, full-time position, based at our European corporate office in Ascot. The Clinical Data Manager will be responsible for ensuring the completion of multiple clinical data management projects according to sponsor and contract requirements in accordance with applicable standard operating procedures. Study lead for Data Project Manager and as appropriate with Sponsor and project team on key issues and progress updates.
Responsibilities include:
Effective management of all data management aspects of assigned project (s) from set up to database lock. Attend regular meetings with the sponsor and project team, for discussions relating to data management issues and provides status updates for the project. Report on quality and performance metrics, including timelines, to DPM and, where required, DM Management. Active participation in the organisation and presentation of in-house and external training courses. Work in strict adherence to SOPs as well as current ICH-GCP guidelines and other applicable standards demanded by the Regulatory Authorities.
Requirements
Qualified candidates will possess a minimum of a Bachelor's degree in a Life Science, Nursing, Computer Science or related discipline. Minimum of 5+ years experience in working with clinical trials data, and experience with the data management process and databases. Proven knowledge of clinical data management process and clinical database systems. Strong oral and written communication skills. Effective working knowledge of Microsoft Office Suite including Word, Excel, and Project. Demonstrated problem solving, analytical, organization, and time management skills. Demonstrated flexibility and ability to work well in a team environment. Full knowledge of clinical data flow and research design. Demonstrated ability to be compliant with GCP/regional regulatory guidelines, SOPs. Extensive experience within the CRO industry. Extensive knowledge of Clinical Data Management System(s), including Electronic Data Capture system(s). Good understanding data standards, preferable CDISC STDM.
For confidential consideration, please submit your CV to hr-uk@pharm-olam.com . NO PHONE CALLS PLEASE.
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If you were eligible to this vacancy, please email us your resume, with salary requirements and a resume to Pharm-Olam International.
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This vacancy starts available on: Fri, 10 Aug 2012 10:50:53 GMT