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01/04 Karan Dhond
Talent Advisor at Randstad

Views:93 Applications:27 Rec. Actions:Recruiter Actions:13

Senior Statistical Programmer - Clinical Data (4-10 yrs)

Hyderabad Job Code: 909471

- The senior statistical programmer will ensure SOPs are followed and timelines and quality are met.

- He/she will support health policy-related research projects conducted by investigators.

- He /she will use standard SAS and/or STATA programming skills to create analytical datasets from clinical trials, surveys and health care claims, to construct and standardize outcome measures and other analytical variables through data cleaning and data manipulation, to provide descriptive and analytical reports, and to perform specialized statistical analyses.

- He/she will implement non-routine macros and advanced techniques to merge different datasets and create analysis files from complex databases.

- He/she will use advanced statistical methods to analyze the data. Strong teamwork and collaboration skills are needed to support multiple projects led by individual investigators.

- Medical global or local teams

- Clinical Trial / Database management teams

- Pharmacovigilance teams

1. People :

- Maintain effectiveness relationships with the end stakeholders (Medical community) within the allocated Global business unit and product - with an end objective to develop statistical programs

- Interact effectively with stakeholders on medical and pharmacovigilance departments

- Feedback from stakeholders (end customers, medical teams) on overall satisfaction

2. Performance :

- Conduct appropriate statistical analyses for biomedical research

- Design, develop, test, implement and document statistical programming in high-level software packages

- Document methods and results through memoranda and reports communicating findings to project team members

- Develop, document, and maintain analytical data files

- Develop design and data analysis plans to support research investigations

- Write and edit statistical methods sections of manuscripts and abstracts for presentations and publications

- Read and review appropriate biomedical and clinical research literature - Adherence to timeline

- Adherence to quality target

- Adherence to timeline

- Adherence to quality target

3. Process :

- Conduct appropriate statistical analyses for biomedical research

- Design, develop, test, implement and document statistical programming in high-level software packages

- Document methods and results through memoranda and reports communicating findings to project team members

- Develop, document, and maintain analytical data files

- Develop design and data analysis plans to support research investigations

- Write and edit statistical methods sections of manuscripts and abstracts for presentations and publications

- Read and review appropriate biomedical and clinical research literature

- Feedback from stakeholders (end customers, medical teams) on satisfaction with services provided

- Adherence to Plan / Calendar

4. Customer :

- Work closely with Medical teams in regions/areas to identify statistical programming needs and assist in developing assigned deliverables

- Liaise with Medical department to prepare relevant & customized deliverables

- Feedback from stakeholders (end customers, medical teams) on satisfaction with services provided

Requirement of the job :

- Advanced SAS and other statistical computing software skills (e.g., R) in a clinical data environment across multiple therapeutic areas, thorough understanding of relational databases and their correlation to submission-ready database structure (CDISC data structure requirements)

Women-friendly workplace:

Maternity and Paternity Benefits

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