Senior Clinical Data ManagerLocation: 1 Day a week onsite in NYCSalary: $140-160k Base plus bonusScientific Search has partnered with a clinical-stage pharmaceutical company pioneering novel approaches to treating cancer. The Senior Clinical Data Manager brings hands-on experience in oncology clinical data management, deep familiarity with Medidata Rave and the ability to work cross-functionally in a fast-paced biotech environment. Responsibilities Own and manage clinical data management activities for assigned early-phase oncology studies, ensuring data quality, integrity, and inspection readiness. Serve as the primary owner and administrator of the company’s Medidata platform, including Cloud Admin configuration and maintenance, user access management, etc. Provide oversight of EDC builds and updates, including review and approval of database specifications and edit check specifications, completion of UAT, etc. Develop and implement data review plans and coordinate ongoing external and internal data cleaning and query management activities. Review data listings to support study oversight and decision-making. Collaborate cross-functionally with Clinical Operations, Clinical Science, Biostatistics, Medical, and external vendors/CROs to ensure alignment and timely data delivery. Monitor data management metrics and reports to ensure compliance with protocols and study plans. Contribute to process improvement, SOP development, and inspection readiness activities as the clinical organization continues to scale. RequirementsBachelor’s degree in life sciences, data science, or a related field. 6+ years of clinical data management experience, with at least 3 years in oncology clinical trials. Prior experience in early-phase (Phase 1/1b/2) oncology trials within a biotech or CRO setting. Extensive hands-on experience with Medidata including Cloud Admin and Rave EDC. Elluminate administration experience a plus Strong understanding of CDISC standards.  Experience working with CROs and vendors, including oversight of outsourced data management activities. Working knowledge of GCP, ICH, and regulatory expectations for clinical data. Highly detail-oriented with strong organizational and problem-solving skills. Adaptable mindset with interest in helping build and scale data management capabilities. How To Apply: We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to tom@scientificsearch.com and tell me why you’re interested. Or, feel free to email your resume. #LI-HYBRID #LI-TO1Type: Direct HireCategory: BiopharmaDate Posted: 2026-02-04