- Efficiently utilizes scanning software to accurately process CRF's used in product studies to be submitted to various governing agencies for approval. CRF acquisition and QC must allow timely and efficient Data Entry and Data review processing by other Clinical and Data Management personnel worldwide.
- Organization and coordination of internal CRF reception activities supporting clinical trials in one or more therapeutic area. Responsibilities include trouble shooting of data collection issues with other Data management and Clinical personnel according to appropriate regulatory and company and departmental guidelines.
- Training new external vendors and in-house temporary personnel on CRF processing as well as the efficient use if the CRF scanning system.
- Responsible for supporting the documentation, testing, implementation, validation and utilization of systems and processes within the Clinical Data Management area.
- Implements data management procedures compliant with Regulatory requirements. Ensures the consistent implementation of procedures, data standards and data coding dictionaries across assigned studies within therapeutic areas.
- Knowledge of utilization of atleast one database system ( such as BBN/Clinical trial, Oracle, Informix, Ingress, Sybase, Access, dbase IV-V, Paradox, DBII).
- Detail-orientation, excellent analytical, problem solving and computer skills.
- Flexible, well oriented, and strong communication and inter-personal skills.
- Excellent organizational, verbal, written and inter-personal skills.
- Ability to work on a multi disciplinary team with multiple priorities.
- Works well under pressure, with initiative to take on unfamiliar tasks.
Experience2 - 4 Years
Education UG - Any Graduate - Any Specialization PG - Any PG Course - Any Specialization
Location Bengaluru/Bangalore
Contact Allergan India PvtLtd
Website http://www.allergan.com
Job Posted 25 Aug
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