| Hyderabad Jobs |
| Banglore Jobs |
| Chennai Jobs |
| Delhi Jobs |
| Ahmedabad Jobs |
| Mumbai Jobs |
| Pune Jobs |
| Vijayawada Jobs |
| Gurgaon Jobs |
| Noida Jobs |
| Hyderabad Jobs |
| Banglore Jobs |
| Chennai Jobs |
| Delhi Jobs |
| Ahmedabad Jobs |
| Mumbai Jobs |
| Pune Jobs |
| Vijayawada Jobs |
| Gurgaon Jobs |
| Noida Jobs |
| Oil & Gas Jobs |
| Banking Jobs |
| Construction Jobs |
| Top Management Jobs |
| IT - Software Jobs |
| Medical Healthcare Jobs |
| Purchase / Logistics Jobs |
| Sales |
| Ajax Jobs |
| Designing Jobs |
| ASP .NET Jobs |
| Java Jobs |
| MySQL Jobs |
| Sap hr Jobs |
| Software Testing Jobs |
| Html Jobs |
| Job Location | Hyderabad |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Medical / Healthcare |
| Functional Area | General / Other Software |
| EmploymentType | Full-time |
266662BRClinical Database DeveloperJob DescriptionDevelop and maintain trial specific database applications, including eCRFs and database specifications, in support of in house and outsourced trials and Program validation and derivation procedures of various levels of complexity within the clinical database management system (such as OC/ RDC, Inform, Rave) using relevant programming languages (SQL, PL/ SQL, C #, VB script, SAS) to support the development of trial specific database applications globally for Phase I- IV with supervision.Your responsibilities:Your responsibilities include, but not limited to- Protocol amendments or required post production changes - Develop database specifications and provide support for outsourced trials - Create, file and maintain appropriate trial documentation - Program and test procedures of various levels of complexity, from documented trial specific requirements, within the clinical database management system using relevant SQL, PL/ SQL, C#, VB script, SAS. - Maintain and update procedures as required for protocol amendments or required post production changes - Creation & execution of trial design reports based on trial metadata - - Understanding of Novartis Clinical Data Standards for procedures developmentMinimum requirements- University or college degree in Life Sciences, Mathematics, Computer Science, Medical Informatics, or equivalent degree Fluent English (Oral and Written) - At least 2- 3 years of experience in clinical database programming, setup of clinical databases and CRF design, procedure / validation programming, as part of the setup of clinical databases, gained in the pharmaceutical industry or CRO as well as the following: - Strong knowledge of SQL, PL/ SQL, C#, VB script, SAS. - - OC/ RDC or INFORM experience preferred - Knowledge of clinical data management systems and/ or relational databases as applied to clinical trialsWhy consider Novartis750 million. That s how many lives our products touch. And while we re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people s livesWe believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you re given opportunities to explore the power of digital and data. Where you re empowered to risk failure by taking smart risks, and where you re surrounded by people who share your determination to tackle the world s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug Development Business UnitGDO GDD CountryIndia Work LocationHyderabad, AP Company/ Legal EntityNov Hltcr Shared Services IndFunctional AreaResearch & Development Job TypeFull TimeEmployment TypeRegular,
Keyskills :
sqlsqlservermysqldatabaseadministrationcustomerrelationsglobaldrugdevelopmentclinicaldatamanagementdatabasemanagementsystemvbscriptcrfdesignlifesciencesclinicaldatadatastandardsatamanag