Key Skills: Sr. Statistical Programmer, It is a global product development services provider with the full-spectrum operational and therapeutic expertise to help pharmaceutical, biotechnology, and medical device companies improve patient care—faster and more efficiently, with less risk and expense

Position Overview:

The Senior Statistical Programmer is a member of the Biostatistics team and plays a lead role in performing all SAS programming tasks required for clinical trial analysis and reporting.

This position works closely with other members of the Biostatistics, and Data Management departments on various clinical projects. May function as Lead Statistical Programmer on multiple projects.

Responsibilities:

This job description serves only as a broad outline of the duties required and will be renewed and amended at periodic intervals in consultation with the Director, Statistical Programming.

Manage or lead assignments and programming personnel on single or multiple projects.

Mentor and train selected associates within the Statistical Programming group.

Participates in the development of and ensures compliance to Standard Operating Procedures (SOPs), policies, and guidelines.

Remain informed of new developments in programming that are relevant to the industry and contribute to the innovation of new reporting systems.

Establish and implement programming standards and comply with regulatory requirements among project team members and across all studies.

Develop standard macros and/or tools in SAS for data analysis and reporting.

Assist with statistical quality assurance review.

Review deliverables before transfer to either internal or external clients.

Ensure that SAS programs developed for specific protocols are effectively portable to other protocols (Reusable code).

Communicate to management on project status and resource issues.

Direct the work of statistical programming services across sites to achieve quality, timely, and cost-effective study deliverables.

Solicit feedback on project profitability from manager or project manager in order to assess and address productivity issues.

May contribute to performance reviews of statistical programmers.
Salary:

INR 6,00,000 - 10,00,000 P.A
Industry:

Pharma, Biotechnology, Clinical Research
Functional Area:

Healthcare, Medical, R&D
Role Category:

R&D
Role:

Bio-Statistician
Keyskills:

SAS, Base, Macros, Clinical Domain
Desired Candidate Profile
Education:

(UG - Any Graduate - Any Specialization) AND (PG - Any PG Course - Any Specialization, Post Graduation Not Required)

B.S. degree required, M.S. degree preferred.

Experience leading SAS programming projects in the pharmaceutical industry demonstrated by the ability to independently act as the point of contact on the statistical programming for all phases of clinical trials, directing the work of one or more programmers.

Proficient in industry standards, medical terminology, and clinical trial methodologies.

Posses project management skills within the Statistical Programming function.

Evidence of the competencies as described in the next section.

It is a global product development services provider with the full-spectrum operational and therapeutic expertise to help pharmaceutical, biotechnology, and medical device companies improve patient carefaster and more efficiently, with less risk and expense