Company: Pharm-Olam International
Location: Bangalore, India
Reference: SDM/INDIA 020116SS
Closing Date: 17 Nov 16
Type: Full Time
Salary (£): Negotiable
Summary of Responsibilities Independently perform all work to satisfy DM Management, DPM and Sponsors. Responsible for ensuring the completion of multiple Data Management projects according to sponsor and contract requirements and 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
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.
MS; BS/RN in Life Sciences and/or combination of education and experience
Minimum of 5-7 years’ experience in clinical data management
Experience / Background / Skills Required
Must have previous experience in a CRO.
Previous eperience with writing Data Management PLans, Data Transfer plans.
Willing to work alternate hours to accomodate sponsor, remote teams. 3+ different eDC experience is required (Rave, Merge, InForm, OC RDC)
Must have experience with multiple external vendors (lab, ePRO, local labs).
Ability to handle multiple study deliverables and timelines.
The Brackens, London Road, Ascot, Berkshire
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