Statistical Programmer

Full Time - India - Posted 7 mins ago - CosMicIT **CosMic IT** - Find Your Dream Job Here_ Hello #Everyone, We at #CosMicIT are looking for #Statistical Programmer Language: #English Locations: #India Summary: 1. 1 to 4 years of experience in programming related activities for clinical studies (Phase I to IV) and publication 2. Advance knowledge of...

Senior Statistical Programmer (6-8 years of exp) Location: Remote ROLES and RESPONSIBILITIES: Perform review of Protocol, Case Report Forms, annotated Case Report Forms, Statistical Analysis Plan, and mock shell Develop and/or validate SDTM domains and ADaM datasets as per the specifications for both Safetyand efficacy Develop and/or validate Tables,...

Senior Statistical Programmer (6-8 years of exp) Location: RemoteROLES and RESPONSIBILITIES:Perform review of Protocol, Case Report Forms, annotated Case Report Forms, Statistical Analysis Plan, and mock shellDevelop and/or validate SDTM domains and ADaM datasets as per the specifications for both Safetyand efficacyDevelop and/or validate Tables,...

The Senior Statistical Programmer will work directly with the stakeholders to lead and contribute to statistical programming projects and to ensure the statistical programming systems, processes and deliverables are aligned with the relevant regulatory requirements. The Senior Statistical Programmer will monitor quality, timelines, resource allocation, and...

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,...

Work Location: Chennai / Bangalore / Hyderabad / Pune / Ahmedabad Please share your updated profile to Experience: 6+ Years ROLES and RESPONSIBILITIES: ·Perform review of Protocol, Case Report Forms, annotated Case Report Forms, Statistical Analysis Plan, and mock shell ·Develop and/or validate SDTM domains and ADaM datasets as per the...

At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where talent, experience and integrity come together to advance the state of clinical development. Working under the direction of Senior Statistical Programmer/Team Lead,...

**Job Code**:SE / GFS / 00623**Job Location**:Multiple Cities / Hybrid / Remote**Experience**:5 -10 years**Requirements**: - Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required. - At least 3 years programming experience in industry recommended. - Demonstrated proficiency in using SAS, R or other...

Cytel provides unrivaled biostatistics and operations research knowledge to our customers in the life sciences industries in the form of both software and services. At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where...

Ability to fill Statistical Programming Lead role on project so Input into and negotiate statistical programming timelines. Ensure that timelines are adhered to. **Responsibilities**: - Coordinate and lead a statistical programming team to successful completion of a study within given timelines and budget. - Monitor project resourcing, project budgets, and...

JOB DESCRIPTIONAbout therole:The Clinical Programmer (SDTM) is primarily responsible for SDTM programming based on Clinical Protocols, eCRF and Statistical Analysis Plans. The Clinical Programmer (SDTM) may also be responsible for data submission packages to clients and regulators. The Clinical Programmer (SDTM) works collaboratively with the project...

**Responsibilities**: - Act as an internal Subject Matter Expert and Work independently to support various programming activities related to analysis and reporting of clinical study data. - Perform as Statistical Programming Coordinator on projects and interact with Sponsors, Data Operation Lead and other functions as a key contact with regard to...

Job Purpose: Serve as a leading role in statistical programming: provide high-level statistical programming support to a wide range of clinical trials as a consultant, both internal and external; make a significant contribution to the statistical programming standardization. The individual also serves as a pivotal role for process and project...

Job Purpose:Serve as a leading role in statistical programming: provide high-level statistical programming support to a wide range of clinical trials as a consultant, both internal and external; make a significant contribution to the statistical programming standardization. The individual also serves as a pivotal role for process and project...

PRIMARY PURPOSE : The Lead Clinical SAS Programmer designs, develops, evaluates and modifies computer programs to analyze and evaluate clinical data, recognizes inconsistencies and initiates resolution of data problems. The Clinical Programmer typically creates programs using SAS to support the clinical research projects.RESPONSIBILITIES : - Collaborate...

PRIMARY PURPOSE : The Lead Clinical SAS Programmer designs, develops, evaluates and modifies computer programs to analyze and evaluate clinical data, recognizes inconsistencies and initiates resolution of data problems. The Clinical Programmer typically creates programs using SAS to support the clinical research projects.RESPONSIBILITIES : - Collaborate...

PRIMARY PURPOSE :The Lead Clinical SAS Programmer designs, develops, evaluates and modifies computer programs to analyze and evaluate clinical data, recognizes inconsistencies and initiates resolution of data problems. The Clinical Programmer typically creates programs using SAS to support the clinical research projects.RESPONSIBILITIES :- Collaborate with...

Title – Technical Lead/Principal Statistical Programmer - Statistical Programming Relevant Experience: 7- 13 years Job ResponsibilitiesExpertise in clinical SAS and hands-on experience in SDTM, ADAM, and TFL. Thorough understanding of the drug development cycle, Biostatistics, and clinical analytics. Have worked on SDTM, Adam, TLF & Macros both on safety...

Title – Technical Lead/Principal Statistical Programmer - Statistical Programming Relevant Experience: 7- 13 years Job Responsibilities Expertise in clinical SAS and hands-on experience in SDTM, ADAM, and TFL. Thorough understanding of the drug development cycle, Biostatistics, and clinical analytics. Have worked on SDTM, Adam, TLF & Macros both on...

Senior Biostatistician (6+ Years of Exp) Location: Remote Roles and Responsibilities: Provide statistical leadership support for clinical studies including study design, sample size calculations, patient randomization, case report form (CRF) review, statistical analyses, interpretation of data, and reporting of results. Coordinate the development of...