Clinical Programmer

1 week ago

Hyderabad, India Worldcare Clinical Full time

**Title**:
Clinical Programmer

**Department**:
Engineering

Support the organization’s mission, vision, and values by exhibiting the following behaviors: excellence and competence, collaboration, innovation, respect, commitment to our community, and accountability and ownership.
Job SummaryPrimary responsibilities are clinical programming and data analysis; understanding various data sources and coding programs to extract data into analysis-ready data sets; creation of software test plans and testing, and development of statistical analysis reports. Data analysis includes descriptive analysis of Independent Reader performance and other metrics to assess the quality of services offered by WCC. Clinical Programmer works closely with Project Managers, Software Developers and Clients regarding data quality and data transfers.Essential Functions
- Lead clinical programming aspects of WCC clinical trials, including consulting with external statistical consultants.
- Analyze existing and new programs, processes and databases to identify and/or guide implementation of modifications aimed at increasing workflow efficiency.
- Develop SAS databases, when applicable
- Review and assure the quality, integrity, accuracy, and completeness of clinical trial data based on project specific guidelines.
- Develop and implement quality review of data using SAS data validation programs.
- Standardize datasets to ensure compliance with data transfer requirements and enhance usability.
- Develop programs and guide efforts to perform robust data manipulation and error detection to ensure data integrity.
- Extract data from the WCC trial system and provide analytical reporting.
- Review data exports and reports to identify, investigate and reconcile data discrepancies with Clinical Operations staff and/or client’s Data Managers.
- Implement variability testing criteria to monitor Independent Reader performance.
- Author and review Data Transfer Files specifications (DTF) for incoming and outgoing data files.
- Respond to client requests for additional data and/or data analysis, as needed.
- Collaborate effectively and build productive relationships within across the global operations team.
- Performs other job-related duties as assigned.

**Qualifications**:

- 4+ years of clinical programming experience in the clinical trials industry required.
- Bachelor's degree in Statistics or computer science preferred.
- Proficiency in data analysis using industry standard tools - SAS and Python required, R optional.
- Proficiency in writing programming code to produce logic checks, derived datasets, summary tables, and figures for data collected via project work.
- Experience with relational databases required; xml and json preferred.
- Working knowledge of clinical trial research, including FDA, GCP/ICH guidelines, GDPR, CDISC/SDTM standards and 21 CFR Part 11
- Proficiency in technical writing with ability to convert complex information into simple readable form.
- Ability to function independently.
- Ability to prioritize and handle multiple tasks and projects concurrently.
- Pinnacle 21 experience a plus

**Salary**: From ₹1,000,000.00 per year

**Benefits**:

- Flexible schedule
- Health insurance
- Internet reimbursement
- Provident Fund
- Work from home

Schedule:

- Flexible shift

Supplemental pay types:

- Yearly bonus

Ability to commute/relocate:

- Hyderabad, Telangana: Reliably commute or willing to relocate with an employer-provided relocation package (required)

**Speak with the employer**
+91 9618840333
- Health insurance

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