Lead Statistician for Clinical Trials

Statistician LeadJob Overview:As a key member of our team, you will work closely with pharmaceutical clients to deliver high-quality statistical programming results. Your primary responsibility will be generating SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies. Additionally, you will develop SAS programs that...

Assuring Clinical Trial Quality:About the RoleAudit clinical research sites across phases I–IV, ensuring compliance and quality standards are met.Responsibilities:Review CRFs, informed consent forms, and regulatory documents to identify areas for improvement.Conduct thorough site audits and provide actionable feedback to support corrective actions.Support...

Job Opportunity:Clinical site auditors are responsible for ensuring compliance and quality at clinical trial sites. This includes conducting site audits, reviewing documentation, and verifying adherence to protocols, GCP, GLP, and regulatory requirements.Audits will be conducted of clinical research sites across phases I-IV.CRFs, informed consent forms, and...

Statistical Programmer PositionAbout the RoleWe are seeking a highly skilled Senior Statistical Programmer to join our team.The ideal candidate will have strong expertise in SDTM, oncology study experience, and proficiency in SAS and R.The successful candidate will possess a good working knowledge of ADaM and TFL programming. Expert-level SAS skills and...

Job Title: Statistical Programming DirectorWe are seeking an experienced Statistical Programming Director to lead our team of statistical programmers in the development and implementation of clinical trial data processing solutions.Responsibilities:Lead a team of statistical programmers in developing and implementing clinical trial data processing...

Seeking a Senior Statistical Programmer with strong expertise in SDTM, SAS, and R. Primary requirements include a proven track record of successful programming in clinical trials, experience with oncology studies, and proficient skills in ADaM and TFL.Responsibilities:Develop and implement efficient data management plans and ensure compliance with CDISC...

Job Title:A Medical Safety Expert is needed to provide medical expertise in evaluating safety data from various sources and determine the medical relevance of serious adverse event reports within the context of a product's safety profile.This role plays a key part as a senior technical leader, participating in matrix management activities including...

Programmer LeadA programmer lead is responsible for the development and maintenance of a global R codebase for CDISC ADaM datasets. This role requires close collaboration with cross-functional teams to understand project-specific data needs.Bachelor's degree in statistics, mathematics, computer science or data scienceMinimum 3 years of experience in R...

Job Title: Clinical Expert in Advanced Robotic Surgery and Medical AIWe are seeking a motivated and skilled professional to collaborate with us as Subject Matter Experts (SMEs) on advanced robotic surgery and medical AI projects. This role offers complete flexibility, allowing you to work part-time and fully remote (flexible hours).Manual data annotation...

Senior Statistical ProgrammerWe are seeking a skilled Senior Statistical Programmer to support comprehensive clinical programming activities across multiple studies.Develop, validate, and maintain clinical trial datasets and outputs using advanced statistical software.Lead and execute the full range of statistical programming deliverables, including creation...