What are the responsibilities and job description for the Clinical Data Analyst position at SciPro Inc.?
Direct message the job poster from SciProHead of Quality - Recruitment - West Coast Contractor - Clinical Data AnalystAbout the Company : We are a clinical-stage precision oncology organization dedicated to developing novel targeted therapies that address frontier challenges in cancer treatment. Our robust R&D pipeline focuses on innovative inhibitors designed to suppress oncogenic variants and enhance combination treatment strategies. Join a team committed to delivering impactful therapies for patients with cancers linked to critical signaling pathways.The Opportunity : As a Clinical Data Analyst, you will support the Clinical Data Programming function by : Collaborating with data managers, statistical programmers, biostatistics, clinical operations, and external vendors to review and finalize data transfer specifications.Ensuring data is received, validated, and meets data integrity standards.Creating or updating data transfer programs and running them according to timelines while adhering to specifications.Reviewing vendor data transfer specifications, including variable lists and attributes.Following Clinical Data Programming guidelines and SAS programming best practices.Monitoring automated jobs and logs.Running Data Review Listings (DRLs) and Study Health Metrics (SHMs) per timelines.Conducting peer reviews of Data Review Listings and reconciliation reports.Using sFTP / FTP clients or vendor portals to manage data downloads and repository postings.Developing new DRLs or study-level reconciliation programs.Supporting and guiding team members within the Clinical Data Programming function.Participating in the development of SAS programming standards, SOPs, and work instructions, including validation and documentation processes.Collaborating with data managers to generate outputs for data cleaning, enhancing data integrity, and ensuring timely and accurate deliverables.Addressing data issues identified by cross-functional teams.Contributing to SAS macro program development and enhancing existing macros to improve project lifecycle efficiency.Utilizing knowledge of CRF annotation, FDA regulations (CDISC, 21 CFR Part 11, ICH, GCP), and other regulatory requirements for submissions.Required Skills, Experience, and Education : MS, BS / BA degree, or equivalent qualification relevant to the field.Proficiency in custom reporting using Business Objects, SAS, Crystal Reports, and Medidata Rave Study Build.7 years of experience in Phases I, II, and III oncology clinical trial studies.Minimum 5 years of oncology-specific experience.Strong multitasking, prioritization, problem-solving, and collaboration skills.Effective written and oral communication abilities.Preferred Skills : SAS certification, experience with Spotfire, Tableau, Power BI, or Windows batch scripting.Python programming knowledge is a plus.Seniority level Not ApplicableEmployment type ContractJob function Information Technology and Science#J-18808-Ljbffr
