Looking for Biostatistical Programming Associate jobs in Hyderabad? Amgen is hiring experienced professionals to join its Clinical Research team in Hyderabad. This opportunity is ideal for candidates with expertise in SAS programming, R programming, CDISC SDTM, ADaM, clinical trial data analysis, and statistical programming within the pharmaceutical or biotechnology industry.
As a Biostatistical Programming Associate, you will support Phase I-IV clinical trials by developing analysis datasets, generating Tables, Listings and Figures (TLFs), validating programming outputs, and contributing to global regulatory submissions. If you have experience in clinical statistical programming and are looking to work with one of the world’s leading biotechnology companies, this is an excellent opportunity.
Job Details
| Details | Information |
|---|---|
| Position | Biostatistical Programming Associate |
| Company | Amgen |
| Department | Research |
| Location | Hyderabad, India |
| Job Type | Full-Time |
| Work Mode | On-site |
| Experience | Minimum 3 Years |
| Qualification | Bachelor’s or Master’s Degree |
| Industry | Biotechnology / Clinical Research |
Key Responsibilities
The selected candidate will be responsible for:
- Perform statistical programming using SAS and R
- Create and validate SDTM, ADaM, and analysis datasets
- Generate Tables, Listings and Figures (TLFs)
- Support safety and efficacy analyses for clinical trials
- Maintain programming documentation and validation records
- Conduct data quality and compliance checks
- Collaborate with global clinical development teams
- Support regulatory submissions and clinical reporting
- Work across multiple clinical studies while maintaining quality standards
Required Qualifications
Applicants should possess:
- Bachelor’s degree in Biostatistics, Statistics, Mathematics, Computer Science, or related scientific discipline
- Minimum 3 years of statistical programming experience in clinical development
- Strong knowledge of:
- SAS Programming
- Clinical Trial Data Analysis
- CDISC SDTM
- CDISC ADaM
- Define Standards
- Familiarity with data quality and compliance tools
- Excellent written and verbal English communication skills
- Ability to manage multiple projects in a global environment
Preferred Qualifications
Candidates with the following will have an advantage:
- MSc or higher qualification in Statistics, Biostatistics, Mathematics, or related field
- Experience with:
- R Programming
- Python
- Automation tools
- SAS/STAT packages
- Previous regulatory submission experience
- Exposure to emerging technologies in statistical programming
Why Join Amgen?
Amgen offers an opportunity to work on innovative biotechnology programs while collaborating with global research teams.
Benefits include:
- Global career development opportunities
- Exposure to international clinical development projects
- Inclusive workplace culture
- Competitive compensation package
- Health and wellness benefits
- Learning and professional growth programs
- Work with cutting-edge clinical research technologies
How to Apply
