Job Opportunity: Associate Statistical Programmer at The Emmes Group
Job Summary
The Emmes Group is seeking a detail-oriented and motivated Associate Statistical Programmer to join our Biometrics team in Bengaluru, India. This is an excellent high-impact opportunity for professionals eager to advance their careers in clinical data science, biostatistics, and SAS programming. As part of a globally recognized Clinical Research Organization (CRO) with over 47 years of industry leadership, you will work on cutting-edge clinical trials across therapeutic areas such as cell & gene therapy, vaccines, rare diseases, and neuroscience. This role provides significant exposure to CDISC standards, regulatory submissions, and real-world clinical datasets.
Responsibilities
As an Associate Statistical Programmer, you will play a vital role in our clinical trial processes. Your core responsibilities include:
- Statistical Programming: Provide robust programming support for clinical trial projects, ensuring high-quality output.
- Code Development: Develop and validate complex programs using Base SAS and SAS Macros.
- Reporting: Generate accurate Tables, Listings, and Figures (TLFs) required for clinical study reporting.
- Data Standards: Implement and maintain CDISC standards, specifically focusing on the creation and validation of SDTM and ADaM datasets.
- Regulatory Support: Assist in the preparation of regulatory submissions for major health authorities (e.g., FDA, EMA) and contribute to safety review reports.
- Quality Assurance: Conduct thorough code validation, peer reviews, and comprehensive documentation to ensure project integrity.
- Compliance: Adhere strictly to internal Standard Operating Procedures (SOPs) and global ICH-GCP guidelines.
- Collaboration: Communicate effectively with cross-functional stakeholders and management regarding project milestones and technical updates.
Requirements
To be successful in this role, candidates should possess the following qualifications and skills:
- Education: A Bachelor’s degree in Life Sciences, Statistics, Mathematics, or a related field.
- Technical Skills: Mandatory proficiency in SAS programming. Knowledge of R or Python is considered a strong advantage.
- Domain Knowledge: A solid understanding of clinical research phases and GCP (Good Clinical Practice) principles.
- Analytical Aptitude: Exceptional problem-solving skills with the ability to interpret complex data requirements.
- Professional Attributes: Detail-oriented, highly organized, and capable of working independently or as part of a collaborative team.
- Industry Familiarity: Basic understanding of CDISC standards (SDTM/ADaM) and clinical data structures is highly desirable.
- Communication: Strong interpersonal skills to effectively engage with global team members.
Why Join The Emmes Group?
Joining Emmes means becoming part of an innovation-driven organization at the forefront of global clinical research. We offer:
- Career Growth: A steep learning curve in clinical data programming within a supportive, professional environment.
- Global Exposure: Opportunities to work on international trials and regulatory submissions that impact global health.
- Advanced Therapeutic Focus: Exposure to high-growth areas like gene therapy and rare diseases.
- Competitive Compensation: We offer a salary range of ₹4.5 LPA – ₹8 LPA, commensurate with experience and industry benchmarks for CROs.
Job Details
- Role: Associate Statistical Programmer
- Location: Bengaluru, India
- Department: Biometrics / Biostatistics
- Job Type: Full-Time
How to Apply
If you are passionate about a career in clinical data science and meet the qualifications listed above, we invite you to apply directly via our official careers portal.
Click here to apply for the Associate Statistical Programmer position at The Emmes Group.
The Emmes Group is an equal opportunity employer committed to fostering an inclusive and innovative work culture.