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Post: Principal Clinical Data Management Programmer
Job Description:
•Supervise and train Data Programming staff
•Interface with PharmaNet/i3 IT staff to ensure proper maintenance of Clinical Data Management Systems (CDMSs), including requests for new instances, database links, etc.
•Ensure the duties of a CDMS support specialist are performed to effect minimal downtime and quick problem resolution
•May act as CDMS Database Administrator by providing new user accounts, user groups, updating user groups and system parameters
•Ensure that all project -related programming tasks are completed in accordance with PharmaNet/i3 standard practices from commencement to closure of a project
•Track milestones and issue status reports, e.g., the status of database release or completion of edict checks
•Participate in the strategic planning for and the management of Data Management related system development projects conducted by IT or external consults
•Assist in the creation and documentation of new or revised departmental procedures
•Design implements project-related reports
•May represent Data Management at Business Development or other sponsor related meetings and at professional meetings
•May coordinate the validation of a CDMS or related supporting software
•May write materials and/or perform technical training for Data Management staff
Candidate Profile:
•Bachelor’s Degree, preferably in Computer science
•In lieu of a Bachelor’s Degree, completion of a certified relational database training program/course work or related web development program/course work, and eight years (total) of relevant experience in data management or system validation
•8-10 years or relevant database programming or system validation experience, including at least two years in a clinical/data management environment
•Advanced competency in database programming or system validation
•Effective verbal and written communication skills
•Ability to serve in a leadership role in clinical database programming or system validation, including mentoring staff and the ability to deal effectively with sponsors and internal customers
•Ability and willingness to travel on occasion
Additional Information:
Experience: 8-10 Years
Location: Hyderabad
Industry Type: Clinical Research
Functional Area: Medical Writing
Last Date: 15th Dec, 2013
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