Lead studies and manage sponsor systems by programming and validating complex datasets and SDTMs. Act as a lead programmer across multiple studies, ensuring quality delivery and coordinating with statisticians and project managers.
PHASTAR
17 Remote Job Openings at PHASTAR
The role involves providing statistical expertise and scientific leadership for pharmaceutical clients, primarily focusing on neuroscience studies. Responsibilities include managing compliance, quality, governance, and people development.
Provide statistical expertise and scientific leadership for global pharmaceutical clients focusing on GI, oncology, neuroscience, or infectious disease studies. Responsibilities include authoring SAP/TLF shells and validating ADaM/TLFs for DMC, IA, and CSR.
Act as a principal/senior programmer to produce complex datasets and outputs for clinical and non-clinical trials. Responsibilities include programming SDTMs, developing complex macros, and serving as the primary point of contact for programming issues.
The role involves programming and validating complex SDTM and ADaM datasets and outputs, specifically within the oncology therapeutic area. The candidate will act as a lead programmer, managing study resources, ensuring SOP compliance, and liaising with statisticians and project managers.
Lead studies and provide technical expertise in programming and validating SDTM datasets and complex efficacy outputs. Responsible for overseeing vendor programming, creating CRT packages, and developing standard macro libraries.
Provide statistical expertise and scientific leadership for GI studies within a cross-functional clinical trial setting. Responsibilities include authoring SAP/TLF shells and validating ADaM/TLFs for DMC, IA, and CSR.
Lead the statistical aspects of clinical trials, including the creation of Statistical Analysis Plans and the validation of complex outputs. Act as a global lead statistician overseeing junior staff and providing consultancy to pharmaceutical and biotech companies.
The role involves programming and validating efficacy datasets, summary tables, and figures according to the Statistical Analysis Plan. The candidate will act as a Lead Statistician, managing project deliverables and collaborating with clients and clinical scientists on study design and sample size calculations.
Lead and deliver SDTM mapping and conversion activities for Real-World Data to CDISC standards. Act as a Subject Matter Expert to develop ECRT packages and collaborate cross-functionally to ensure quality delivery.
The role focuses on providing statistical expertise and scientific leadership for a key pharmaceutical client within the FSP function. Responsibilities include overseeing technical analysis, people development, and ensuring compliance and quality governance.
The role involves providing statistical expertise and scientific leadership for oncology studies within a pharmaceutical client's FSP function. Responsibilities include managing compliance, quality, governance, and people development.
Lead data management for clinical trials, providing expert guidance to project teams and ensuring data integrity across all trial phases. Coordinate data processing activities, implement CDASH standards, and manage communication between functional teams and clients.
The role involves programming and validating complex efficacy datasets, summary tables, and figures for clinical trials. It also requires producing and reviewing Statistical Analysis Plans (SAPs) and other critical study documentation.
Provide statistical expertise and scientific leadership for GI and Oncology studies within a pharmaceutical client setting. Responsibilities include authoring SAP/TLF shells and validating ADaM/TLFs for DMC, IA, and CSR.
The role involves providing statistical expertise and scientific leadership for cardiovascular, renal, and metabolic studies. Responsibilities include authoring SAP/TLF shells, reviewing ADaM/TLFs, and providing input to protocols.
The role involves providing statistical expertise and scientific leadership for pharmaceutical studies in oncology, GI, neuroscience, or infectious diseases. Responsibilities include managing compliance, quality, governance, and leading people development within the FSP team.
