3.0 - 7.0 years

0 Lacs

telangana

On-site

Role Overview: As a Statistical Programmer II at Syneos Health, you will be part of a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. Our Clinical Development model prioritizes putting the customer and patient at the center of our work, aiming to simplify processes and innovate as a team to make a difference in people's lives. Key Responsibilities: - Utilize advanced proficiency in Base SAS, SAS Macro, and SAS SQL for clinical trial data analysis and reporting - Demonstrate in-depth knowledge of CDISC standards to develop ADaM specifications and datasets for regulatory submissions - Produce high-quality Tables, Listings, and Figures (TFLs) covering safety and efficacy endpoints - Experience in programming patient narratives is considered a strong asset - Prepare Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) for submission packages - Conduct Pharmacokinetics (PK) and Pharmacodynamics (PD) data analysis, including non-compartmental analysis and support for modeling activities - Preferred experience in Oncology, Neuroscience, and Immunology studies Qualifications Required: - 3-4.5 years of experience in statistical programming - Technical expertise in SAS Programming, ADaM Dataset Development, TFL Generation, and PK/PD Analysis - Background in Therapeutic Area Expertise with experience in Oncology, Neuroscience, and Immunology studies (Note: The job description may not be exhaustive and additional tasks, duties, and responsibilities may be assigned at the company's discretion. Equivalent experience, skills, and education will also be considered for the role.),

Posted 1 day ago

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Senior SAS Programmer Navitas Life Sciences

5.0 - 9.0 years

0 Lacs

chennai, tamil nadu

On-site

You will be part of our team as a Senior SAS Programmer, where you will be responsible for providing SAS programming support for TFL generation and offering statistical/programming inputs for CRF design and review. Additionally, you will be involved in developing and validating standard and ad-hoc SAS macros. You will carry out reviews of CRF and aCRF, statistical analysis plans, and programming specifications for efficacy variables. Validating Safety Tables using SAS and ensuring the validation of ADaM and derived datasets will also be part of your responsibilities. Furthermore, you will be involved in validating SDTM datasets and their specifications while adhering to the required training. Desirable Skills and Experience: - Proficiency in SAS programming - Expertise in SDTM and ADaM datasets This position is based in Chennai, India, and requires a Graduate or Post Graduate with a degree in life sciences. The role falls under the managerial category within the Data Sciences department and is a full-time position.,

Posted 2 days ago

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Assoc. Principal Stat Programmer Iqvia Biotech

2.0 - 6.0 years

2 - 6 Lacs

Bengaluru, Karnataka, India

On-site

Minimum 10+ years experience with ADaM and TFL programming Experience in Oncology/Immunology studies on Efficacy ADaMs and TFLs (ADTTE PFS, OS, DOR, BOR, ORR is must) Experience on KM Plots, waterfall plot, Forest plot is required, Phase 2,3 Preferable experience, IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries

Posted 2 months ago

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