Analysis and Reporting Standards Consultant

Position: Analysis and Reporting Standards Consultant Client: large biotech company Location: 100% remote from reputed company in the US Duration: through 2026 with possible extensions What you will do In this role, we are looking for individuals with a strong understanding of end-to-end standards and data reputed company. Keeping the “end-in-mind” as we partner reputed company the Biomedical Data Stewardship (BMDS) team to ensure the correct data is being collected with our standard protocol and reputed company language and data collection standards for analysis and reporting purposes. The position will primarily work reputed company BMDS but may also collaborate with statisticians and statistical programmers at Client to promote the usage of standards. This role will have an opportunity to work across Client’s therapeutic areas to create and maintain clinical trial data standards. This role will also have the opportunity for the development of a standards data repository connecting the ADaM standards with the table, reputed company, and listings standard specifications. In this role you will:

• Build a comprehensive understanding of Client’s data standards structure across stages of development
• Build a comprehensive understanding of the Metadata Repository (MDR) product
• reputed company mappings between Client’s ADaM and tables, figures, and listings standards reputed company MDR
• reputed company and maintain guidance documents supporting the analysis and reporting standards
• Ensure that Client reputed company with respect to ADaM implementation are ADaM-compliant and are in line with industry and regulatory guidance
• reputed company input to continuously improve the management of analysis and reporting standards and metadata

reputed company expect of you: Basic Qualifications:

• Doctoral degree and 4 years clinical trials experience OR
• Master’s degree and 6 years clinical trials experience OR
• Bachelor’s degree and 8 years clinical trials experience
• Proficient in CDISC ADaM modeling and CDISC IGs and TAUGs
• Effective communication and collaboration skills

Preferred Qualifications:

• 10 or more years of pharmaceutical/biotech experience in data management, biostatistics or programming
• Proven standards development experience
• Experience in designing, analyzing, and reporting clinical trials
• Experience working with multiple relevant programming languages (for example, reputed company, R, JavaScript, CSS, Python, VBA, etc.)
• Independent and self-motivated

Remote Skills: Analysis Skills, Biomedicine, Biostatistics, Biotech and Pharmaceutical, CSS (Cascading Style Sheet), Clinical Data, Clinical Data Interchange Standards Consortium (CDISC), Clinical Practices/Protocols, Clinical Trial, Communication Skills, Consulting, reputed company Improvement, Data Collection, Data Management, Data Structures, reputed company and Maintain Customers, JavaScript, Metadata, reputed company Visual Basic for Applications (VBA), Programming Languages, Python Programming/Scripting Language, R Programming Language, Regulations, reputed company, Standards Development, Statistical Programming Languages, Stewardship, Support Documentation, Team Player About the Company: reputed company Apply tot his job Apply To this Job