Statistical Programmer
Sun Pharmaceutical Industries, Inc., Indiana, PA, United States
JOB DESCRIPTION
Location: Remote/Hybrid
Responsibilities
In this role, a typical day might include:
Lead statistical programming activities for a therapeutic area or compound/indication within multiple studies/projects in various study activities to ensure timely and high-quality programming deliverables in assigned projects and areas.
Develop and maintain programming documentation following programming standards and processes. Create CDISC standard SDTM mapping specifications and ADaM specifications.
Develop and oversee the development of SAS programs for the creation of SDTM and ADaM datasets following CDISC standards and reports (Tables, Listings and Figures).
Contribute to the development of standard macros, participate in establishing and maintaining statistical programming standards.
Participate in the CRF annotation, review of SAP, TLFs specifications development and TLFs review.
Handle all P21 related items and eCRT package including aCRF, define.XML, cSDRG, ADRG and ARM for the regulatory submission to FDA/EMA/PMDA or other agencies.
Support global regulatory authority submissions following the guidelines (sdTCG, DSC, eCTD etc.) and working closely with partnering functions to address health authority requests.
Demonstrate company values by demonstrating excellence, competence, collaboration, innovation, respect, ownership, team work and accountability.
Understand the scope of work, plan and complete the deliveries and timelines with the study team, programming lead and management.
Participate and contribute towards department goals, SOPs, training guidelines and SME topics.
Mentor and coach new hires and junior programmers.
Qualifications
Proficiency in SAS programming skills in a clinical data environment with excellent analytical skills. Working knowledge of other programming languages such as R, Python, etc. is a plus.
Excellent knowledge of pharmaceutical clinical development (i.e., understanding of statistical concepts, techniques, and clinical trial principles) and regulatory submissions (NDA, ANDA, etc.).
Excellent working knowledge of implementing CDISC standards, regulatory guidance and TAUG.
Ability to work independently and on global interdisciplinary teams. Good organizational, interpersonal, and communication skills. Positive attitude, team player and growth mindset.
Problem solving and innovative skills that demonstrate initiative and motivation.
Hands‑on programming as well as people and process management experience.
Demonstrated and applied SAS programming skills. SAS certificates a plus.
Minimum Requirements
Minimum Bachelor’s degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline.
2-12+ years of programming experience in processing clinical trial data in the biotechnology, pharmaceutical, CRO or health care related industry.
Benefits
At Sun Pharma, your success and well‑being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth.
Disclaimer
The preceding job description has been designed to indicate the general nature and level of work performed by an employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).
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Location: Remote/Hybrid
Responsibilities
In this role, a typical day might include:
Lead statistical programming activities for a therapeutic area or compound/indication within multiple studies/projects in various study activities to ensure timely and high-quality programming deliverables in assigned projects and areas.
Develop and maintain programming documentation following programming standards and processes. Create CDISC standard SDTM mapping specifications and ADaM specifications.
Develop and oversee the development of SAS programs for the creation of SDTM and ADaM datasets following CDISC standards and reports (Tables, Listings and Figures).
Contribute to the development of standard macros, participate in establishing and maintaining statistical programming standards.
Participate in the CRF annotation, review of SAP, TLFs specifications development and TLFs review.
Handle all P21 related items and eCRT package including aCRF, define.XML, cSDRG, ADRG and ARM for the regulatory submission to FDA/EMA/PMDA or other agencies.
Support global regulatory authority submissions following the guidelines (sdTCG, DSC, eCTD etc.) and working closely with partnering functions to address health authority requests.
Demonstrate company values by demonstrating excellence, competence, collaboration, innovation, respect, ownership, team work and accountability.
Understand the scope of work, plan and complete the deliveries and timelines with the study team, programming lead and management.
Participate and contribute towards department goals, SOPs, training guidelines and SME topics.
Mentor and coach new hires and junior programmers.
Qualifications
Proficiency in SAS programming skills in a clinical data environment with excellent analytical skills. Working knowledge of other programming languages such as R, Python, etc. is a plus.
Excellent knowledge of pharmaceutical clinical development (i.e., understanding of statistical concepts, techniques, and clinical trial principles) and regulatory submissions (NDA, ANDA, etc.).
Excellent working knowledge of implementing CDISC standards, regulatory guidance and TAUG.
Ability to work independently and on global interdisciplinary teams. Good organizational, interpersonal, and communication skills. Positive attitude, team player and growth mindset.
Problem solving and innovative skills that demonstrate initiative and motivation.
Hands‑on programming as well as people and process management experience.
Demonstrated and applied SAS programming skills. SAS certificates a plus.
Minimum Requirements
Minimum Bachelor’s degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline.
2-12+ years of programming experience in processing clinical trial data in the biotechnology, pharmaceutical, CRO or health care related industry.
Benefits
At Sun Pharma, your success and well‑being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth.
Disclaimer
The preceding job description has been designed to indicate the general nature and level of work performed by an employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).
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