
Clinical Programmer
10 hours ago
**Summary**:
- Responsible to support all statistical programming/data review reporting and analytics development aspects of assigned studies or project-level activities.
**About the Role**:
**Major accountabilities**:
- 1.Produce and track reports for various line functions within Global Drug Development, used for ongoing monitoring of clinical data
- 2. Provide understandable and actionable reports on clinical data and monitoring of clinical data for key stakeholders
- 3. Facilitate interaction with end-user on creating specifications and working with programmers or performing the programming activities for successful delivery
- 4. To provide quantitative analytical support to the global program teams, including providing support on analyzing reports
- 5. Support the planning, execution and close-out of Clinical Programs/Trials.
- 6. Support the management in collation and delivery of analytics reports for critical decision making
- 7. Create, file and maintain appropriate documentation
- 8. Work with the internal SMEs and key stakeholders in providing analysis and interpretation of clinical program/trial operational data
- 9. Provide necessary training to end-user on best / appropriate and consistent use of various data review tools
- 10. Program reports of various complexity from documented requirements, within the clinical reporting systems using SQL, PL/SQL, C#, VB script, SAS, Python, R
- 11. Good understanding of Novartis Clinical Data Standards and its implementation for creation of reports specifications or reports output
**Key performance indicators**:
- A Quality and timeliness of deliverables
- 2. Revisions to deliverables caused by logic or programming errors
- 3. Customer feedback and satisfaction
**Minimum Requirements**:
**Work Experience**:
- 2-5 years of experience in clinical review and reporting programming, business analytics and/or clinical trial setup, gained in the pharmaceutical industry, CRO or Life Science related industry as well as the following:
- 2. Strong knowledge of programming languages (SQL, PL/SQL, C#, VB script, SAS, Python, R)
- 3. Knowledge of Data Review and/or Business Intelligence tools (such as Spotfire, JReview)
- 4. Understanding of clinical data management systems and/or relational databases as applied to clinical trials
- 5. Attention to detail, quality, time management and customer focus
- 6. Ability to translate technical concepts for nontechnical users in the areas of clinical database design and data review reporting development
- 7. Strong verbal and written communication skills to work with our global partners and customers
- 8. Understanding of Drug Development Process, ICHGCP, CDISC standards and Health Authority guidelines and regulation
Division
Development
Business Unit
Innovative Medicines
Location
India
Site
Hyderabad (Office)
Company / Legal Entity
IN10 (FCRS = IN010) Novartis Healthcare Private Limited
Functional Area
Research & Development
Job Type
Full time
Employment Type
Regular
Shift Work
No
**Accessibility and accommodation**:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
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