Direct message the job poster from SciPro Head of Quality - Recruitment - West Coast This role is for a Clinical Data Analyst with EXTENSIVE SAS Experience. Candidates must have hands-on, technical experience and knowledge of utilizing SAS within Clinical Data Analysis for Clinical Trials in the Biotech/Pharmaceutical Industry. Candidate will need to be based close to South San Francisco, as this role will be on average 3 days a week on site. The client is growing rapidly and looking for support as they gear up for NDA Submission. Contractor - Clinical Data Analyst About 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. Participating in the development of SAS programming standards, SOPs, and work instructions, including validation and documentation processes. Contributing to SAS macro program development and enhancing existing macros to improve project lifecycle efficiency. 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. 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. 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 Mid-Senior level Employment type Contract Job function Science and Research Industries: Biotechnology Research, Research Services, and Pharmaceutical Manufacturing #J-18808-Ljbffr SciPro
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