Remote Life Science Job at Sun Pharma
Looking for a high-growth Remote Life Science Job in the pharmaceutical industry? Sun Pharmaceutical Industries Ltd. is hiring a Senior Executive – Statistical Programming to support global clinical development programs. This exciting opportunity is ideal for professionals with experience in clinical trial data programming, SAS, CDISC standards, and regulatory submissions. If you’re searching for Sun Pharma Careers or exploring advanced Statistical Programming Jobs, this remote/hybrid position offers the chance to contribute to global Phase I-IV clinical studies while working with one of India’s leading pharmaceutical companies.
About Sun Pharma Careers
Sun Pharmaceutical Industries Ltd. is one of the world’s leading specialty generic pharmaceutical companies. With a strong global presence across multiple therapeutic areas, Sun Pharma focuses on innovation, quality, and patient-centric healthcare solutions. Through continuous investment in research and development, the company contributes significantly to global healthcare advancements. Professionals pursuing Sun Pharma Careers benefit from a collaborative environment, global exposure, career development opportunities, and the chance to work on impactful pharmaceutical and clinical research programs.
Job Details:
- Job Title: Senior Executive, Statistical Programming
- Company: Sun Pharmaceutical Industries Ltd
- Business Unit: Global Clinical Development
- Job Grade: Senior Executive
- Location: Gurgaon – R&D (Remote/Hybrid)
Job Summary
The Senior Executive, Statistical Programming supports one or more Phase I–IV studies programming activities in alignment with project strategies. The role operates within a team environment to implement and execute programming and project standards that support ongoing clinical studies, study reports, regulatory submissions, and ad hoc/post hoc analyses.
The incumbent works closely with the Programming Team Lead (PTL), internal partner functions, and external functional service providers to ensure programming deliverables are completed on time and with high quality.
Key Responsibilities
Statistical Programming Support
- Supports statistical programming activities for therapeutic areas or compound/indication programs across multiple studies and projects.
- Ensures timely and high-quality programming deliverables within assigned projects and areas.
Documentation & Standards
- Updates and maintains programming documentation in accordance with programming standards and processes.
- Updates CDISC standard SDTM mapping specifications and ADaM specifications.
Dataset & Report Development
- Develops and validates SAS programs for the creation of:
- SDTM datasets
- ADaM datasets
- Tables
- Listings
- Figures (TLFs)
- Ensures compliance with CDISC standards.
Programming Standards & Utilities
- Contributes to the development of standard and utility macros.
- Participates in establishing and maintaining statistical programming standards.
CRF & TLF Development
- Participates in:
- CRF annotation
- TLF specification development
- Macro development
Regulatory Submission Support
- Contributes to P21-related deliverables and eCRT packages, including:
- aCRF
- define.XML
- cSDRG
- ADRG
- ARM
- Supports regulatory submissions to agencies such as:
- FDA
- EMA
- PMDA
- Other global health authorities
Regulatory Compliance
- Supports global regulatory authority submissions following:
- sdTCG
- DSC
- eCTD guidelines
- Collaborates with partnering functions to address health authority requests.
Company Values & Collaboration
- Demonstrates company values through:
- Excellence
- Competence
- Collaboration
- Innovation
- Respect
- Ownership
- Teamwork
- Accountability
Project Management
- Prioritizes and manages assignments based on business needs.
- Understands project scope and delivery timelines.
- Plans and completes deliverables in coordination with study teams, programming leads, and management.
- Performs end-to-end programming activities while contributing as a team player.
Required Skills & Competencies
Technical Skills
- Strong SAS programming skills within a clinical data environment.
- Excellent analytical skills.
- Knowledge of additional programming languages such as:
- R (preferred)
- Python (preferred)
Clinical & Regulatory Knowledge
- Good understanding of:
- Pharmaceutical clinical development
- Statistical concepts and techniques
- Clinical trial principles
- Regulatory submissions (NDA, ANDA, etc.)
CDISC Expertise
- Working knowledge of:
- CDISC standards
- Regulatory guidance
- TAUG
Professional Competencies
- Strong attention to detail.
- Quick learning ability.
- Adaptability to fast-paced environments.
- Ability to work independently and within global interdisciplinary teams.
- Strong organizational, interpersonal, and communication skills.
- Positive attitude and growth mindset.
- Problem-solving and innovation-oriented approach.
- Demonstrated SAS programming expertise.
- SAS certifications are considered an advantage.
Educational Qualification
- Minimum Bachelor’s Degree in Life Sciences & Related disciplines
Experience
- Minimum 2+ years of programming experience involving clinical trial data within:
- Biotechnology companies
- Pharmaceutical companies
- Contract Research Organizations (CROs)
- Healthcare-related industries
