Statistical Programmer

**About the Role** Location : Remote (India) **Key Responsibilities** - Develop, validate, and maintain SAS programs to generate analysis datasets (ADaM, SDTM) and TLFs for clinical trial submissions. - Ensure programming deliverables are accurate, efficient, and compliant with CDISC standards and regulatory guidelines. - Collaborate with Biostatistics and...

As a member of Parexel’s Statistical Programming group, you will be heavily involved in leading trials to successful completion, working in close collaboration with sponsor teams, and Parexel teams in differing locations. Depending on your career goals, you will be provided the opportunity to be exposed to a variety of different sponsors, products and...

**Jr Statistical Programmer** **Location: Bangalore-Homebased** As a **Statistical Programmer** you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: - Develop understanding of all applicable policies and procedures - Completes programming activities...

**Description** **Statistical Programmer I** Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient...

The Statistical Programmer II provides technical expertise for the conduct of clinical trials, and works with mínimal supervision to support various programming activities related to the analysis and reporting of clinical study data. In addition, the Statistical Programmer II may fill the Statistical Programming Lead role (or part of that role) on small,...

**Description** **Statistical Programmer II** Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient...

Overview: Work as a principal programmer across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...

**Key Accountabilities**: **Project Management**: - Ability to fill Statistical Programming Lead role on projects - Input into and negotiate statistical programming timelines. Ensure that timelines are adhered to. - Coordinate and lead a statistical programming team to successful completion of a study within given timelines and budget. - Monitor project...

Overview: THE COMPANY Phastar is a multiple award-winning global biometric Contract Research Organization (CRO) that is accredited as an outstanding company to work for by Best Companies. We partner with pharmaceutical, biotechnology and medical device organizations to provide the expertise and processes to manage and deliver on time, quality biostatistics,...

**Key Accountabilities**: **Project Management**: - Ability to fill Statistical Programming Lead role on projects - Input into and negotiate statistical programming timelines. Ensure that timelines are adhered to. - Coordinate and lead a statistical programming team to successful completion of a study within given timelines and budget. - Monitor project...