Cdisc Standards Jobs in Dallas, GA

The Manager of Statistical Programming is a strategic role which guides a team of Statistical Programmers in the research and development of new pharmaceutical products. This role is directly responsible for leading the statistical programming activities for a compound/indication or t More...

Responsibilities: Serve as the principal programming lead across multiple studies or a clinical program ensuring timely accurate and regulatory-compliant deliverables. Lead or contribute to the development validation and documentation of SDTM ADaM and TFLs in support of clinical stud More...

Solution IT Inc. is looking for OIC/VBCS Technical Consultant for one of its clients Remote Job Title: OIC/VBCS Technical Consultant Required Skills: Proficiency in building custom applications and extending Oracle Cloud functionality through VBCS. Experience with ORDS and OIC i More...

What We Can Achieve Together:The Associate Director of Development situated in Dallas TX works closely with the development team to plan implement and coordinate effective multi-year strategies and plans for Dallas area gift prospects focused on individual giving but can include corpo More...

CD PROJEKT RED is looking for a Senior Gameplay Programmer to join our team to work on Cyberpunk 2 the follow-up to Cyberpunk 2077. In this role you will collaborate with our team working in Unreal Engine 5 to build new mechanics and features to generate compelling game More...

The Senior Manager of Statistical Programming is a leadership role which manages a team of statistical programmers in the research and development of new pharmaceutical products. The Senior Manager of Statistical Programming is responsible for leading the statistical programming activ More...

Roles & Responsibilities: MS in Statistics Computer Science or a related field with 5 years of relevant experience. or BS in Statistics Math Computer Science or a STEM related field with 8 years of relevant experience. SAS certification. Group setting SAS EG and Unix environment. SAS More...

Thank you for your interest in joining our team! QVC Group Inc. is a Fortune 500 company with six leading retail brands QVC HSN Ballard Designs Frontgate Garnet Hill and Grandin Road. We are a live social shopping company that redefines the shopping experience through video-driven co More...

Responsibilities: Lead and manage clinical data management activities for oncology clinical trials ensuring adherence to project timelines budgets and quality standards. Provide strategic oversight and direction to CRO clinical data management teams for assigned studies. Develop and More...

Responsibilities: Leads all DM lifecycle activities from study start-up maintenance database lock and close-out. Independently develop DM documents including but not limited to Data Management Plans (DMP) Case Report Forms (CRFs) CRF Completion Guidelines Edit Checks UAT specificatio More...

Responsibilities: Position leads complex studies in study design statistical analysis and interpretation of results with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted to Health More...

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation review completion and delivery of statistical programming activities and deliverable More...

Position OverviewAt PNC our people are our greatest differentiator and competitive advantage in the markets we serve. We are all united in delivering the best experience for our customers. We work together each day to foster an inclusive workplace culture where all of our employees fe More...

Responsibilities: Providing statistical programming support to generate tables listings and figures for assigned projects. Demonstrating proficiency in CDISC SDTM and Adam to support various submission activities including IA CSR DSUR and publications. Overseeing all aspects of stati More...

Responsibilities: Lead clinical data management activities for multiple complex studies from study startup to database lock and final reporting. Develop and manage data management timelines for multiple projects ensuring all milestones are met according to project plans. Design build More...

Responsibilities: To support the Biostatistics team by carrying out programming activities of statistical programmers and overseeing external vendors (as required) and to ensure timely and accurate programming and validation activities for clinical studies and publications. Contribut More...

Responsibilities: Develop and maintain all data management documentation including case report forms data management plans edit check specifications data review plans and data transfer agreements. Design case report forms (CRFs) for electronic data capture (EDC) systems for data coll More...