Statistical Programmer 2 in Hyderabad, India - Jobeax
Vacancy description
Statistical Programmer 2 in Hyderabad, भारत
IQVIA
Hyderabad, भारत
IQVIA seeks a Statistical Programmer 2 to develop analysis plans, write detailed specifications, and author statistical study report sections. The role involves mentoring junior staff, leading biostatistical teams on assigned studies, and ensuring high-quality deliverables aligned with clinical trial standards.
Responsibilities
Author analysis plans, statistical specifications, and quality control reviews of SAPs and programming shells.
Program datasets, tables, listings, and figures to industry standards while ensuring accuracy and consistency.
Lead biostatistical teams on individual studies, coordinating with project leads and managing timelines and budgets.
Review data management activities, resolve data issues, and assist with database lock and unblinding processes.
Mentor junior and new staff, provide training on operational procedures, and support clinical study report development.
Requirements
Bachelor's degree in biostatistics or related field with 5 years relevant experience, or Master's degree with 5 years experience, or Ph.D.
1-3 years prior relevant experience in statistical programming or clinical research.
Advanced knowledge of clinical trial statistical methods and regulatory standards (GCP, ICH guidelines).
Proficient in SAS programming with familiarity of StatXact or similar statistical packages.
Excellent written and oral communication skills with strong attention to technical detail.
Knowledge of CDISC standards and database lock/unblinding processes.
Strong organizational skills and individual initiative in complex project environments.
Senior Statistical Programmer 2 role at a global CRO involves leading programming initiatives, developing and validating clinical datasets using SAS, and providing consultancy on CDISC standards and regulatory submissions. The position requires mentoring team members and driving continuous improvement across biostatistical ...
... interact with each other, customers, patients and suppliers. As a Statistical Programmer II at ICON, you will the development, validation, and execution of statistical programs to support clinical trial analysis and reporting. What You Will Do: - Developing, validating, and maintaining complex statistical programs (SAS, ...
Johnson & Johnson seeks an experienced statistical programmer to support clinical trial data analysis and reporting activities. The role involves designing and developing programs for clinical research, ensuring CDISC compliance, and collaborating with cross-functional teams on trials of low to medium complexity. Responsibilities ...
JOB DESCRIPTION Work Schedule Second Shift (Afternoons) Environmental Conditions Office Job Description Principal Programmer Analyst – End-to-End SDTM Join Us as a Principal Programmer Analyst – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than ...
... Statistical programming lead for large global or other major programs.- Act as SME & provide technical solutions and advice to the staff and to clients on statistical programming.- Act as subject matter expert for large-scale complex projects, providing hands-on support for the completion of projects and solve critical ...
... the Project Team Lead and supervisor to deliver on time, with high quality and within budget. Build and maintain effective customer relationships, driving statistical discussions, providing support and/or guidance for statistical activities. Demonstrates and promotes efficient communication. If in lead role, runs meetings, ...
ICON seeks a Statistical Analyst to support clinical trial activities, including study design input, statistical methods documentation, and SAS-based programming. The role involves collaborating across teams to deliver high-quality statistical analyses and study deliverables. Responsibilities - Support study initiation ...
... science and innovation to develop life-changing medicines for people with serious https://jobeax.com/link/QBe1ZamoJXmfvWX4 are seeking an Associate Manager, Statistical Programming - Central Services to join our Statistical Programming team, supporting integrated analysis, regulatory submissions, and clinical trial disclosure ...
Associate Director of Statistical Programming in the Oncology Biometrics department, responsible for leading statistical programming activities across clinical drug development, regulatory submissions, and commercialization efforts. Reports to the Director of Statistical Programming at a hybrid role in Bangalore. Responsibilities ...
Thermo Fisher Scientific seeks a Senior Programmer Analyst to lead bioinformatics programming on clinical trial projects of moderate complexity. The role involves developing statistical programs, managing multidisciplinary teams, and mentoring junior programmers while supporting centralized monitoring and risk-based quality ...