About this role
The team is seeking a Senior Statistical Programmer with expertise in Clinical SAS and CDISC standards. This role is pivotal in supporting clinical trials and ensuring the integrity and accuracy of statistical data analysis. The position is fully remote, allowing candidates from across India to apply.
Key Responsibilities:
- Develop and validate SAS programs for statistical analysis and reporting of clinical trial data.
- Ensure compliance with CDISC standards and regulatory requirements.
- Collaborate with biostatisticians and clinical teams to interpret data and provide insights.
- Prepare and maintain documentation for programming processes and outputs.
- Participate in project meetings and contribute to the development of project plans.
Required Skills & Qualifications:
- Strong proficiency in SAS programming, particularly in a clinical trial environment.
- In-depth knowledge of CDISC standards (SDTM, ADaM).
- Experience in data management and statistical analysis.
- Familiarity with regulatory guidelines and clinical trial processes.
- Excellent problem-solving skills and attention to detail.
Experience:
- 5-8 years of relevant experience in statistical programming within the pharmaceutical or biotechnology industry.
What we offer:
- An opportunity to work with a dynamic team in a remote setting.
- Professional development and growth opportunities.
- A collaborative work environment that values innovation and expertise.
Applications are read by our talent team, usually within two working days.
If you look like a fit we will call you, and you will hear from us either way.