Senior Clinical Database Programmer Job in Parexel International Corporation
Senior Clinical Database Programmer
Parexel International Corporation
4+ weeks ago
- Hyderabad, Telangana
- Not Disclosed
- Full-time
- Permanent
Job Summary
Knowledge of SOPs/Guidelines/Work Instructions/System Life Cycle methodologies, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application.
Experience working with at least two systems used within the Clinical Trial process (e.g. SAS, CDMS, EDC: Inform, RAVE, DataLabs, Medrio, Veeva, CTMS, Medical Safety Reporting) is desirable. Build Certified in at least one system, if available
Strong experience in the clinical research industry or a similar field is required
Knowledge of Software Development Life Cycle (SDLC) methodologies. Knowledge of GCP, 21CFRPart11, and other relevant ICH/regulatory guidelines
Bachelor s degree (or equivalent) in a relevant science discipline is preferred or equivalent work experience
In addition, the Senior Database Programmer can assist the Database Primary or Technical Lead role on projects, and liaise with sponsors, Data Management Lead, and other functional areas as required. General areas of responsibility also include eCRF design, edit check programming, and integration of third-party systems with the EDC databases. All tasks should be performed in accordance with corporate quality standards, SOPs/Work Instructions/Guidelines, ICH-GCP, and/or other international regulatory requirements.
Qualifications
Experience in at least one programming environment (e.g. SAS, CDMS, EDC, SQL, VB, Java).Knowledge of SOPs/Guidelines/Work Instructions/System Life Cycle methodologies, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application.
Experience working with at least two systems used within the Clinical Trial process (e.g. SAS, CDMS, EDC: Inform, RAVE, DataLabs, Medrio, Veeva, CTMS, Medical Safety Reporting) is desirable. Build Certified in at least one system, if available
Strong experience in the clinical research industry or a similar field is required
Knowledge of Software Development Life Cycle (SDLC) methodologies. Knowledge of GCP, 21CFRPart11, and other relevant ICH/regulatory guidelines
Experience Required :
Fresher
Vacancy :
2 - 4 Hires
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