Clinical Data and Monitoring LeadSouth San Francisco, California, United StatesRole: Clinical Data and Site OperatorThis role owns the operational execution and data integrity of the NEW study. Crucially, this is an execution and triage role, not a final Medical Monitor role. The clinical safety and eligibility decisions reside with the company's internal MDs.
This position ensures the data reaching the MDs is clean, timely, and actionable.Summary:Remote & Onsite Data Verification (Replacing RMV & IMV)Clean, fully verified EDC data ready for sponsor review, delivered via tech-enabled efficiency rather than brute-force hourly logging.Execute 100% Source Data Verification (SDV) directly across EMRs (Epic/Cerner) and Medidata Rave.Efficiently process high-volume log lines (ConMeds, AEs, Transfusions) specific to Sickle Cell and Cell Therapy.Clinical Triage & Signal DetectionSynthesized safety summaries and flagged clinical events requiring MD attention.Act as the first line of clinical review. You are not making the final medical call; you are separating the "noise" (routine lab variances) from the "signals" (Grade 3+ AEs, VOCs, DLTs) so the internal Medical Monitor (CEO/MD) can make rapid, informed decisions.Site Activation & Expansion (Replacing SIV & PSSV)"Ready-to-Enroll" clinical sites fully trained on Kamaus complex cell therapy logistics.Conduct targeted Pre-Study (PSSV) and Site Initiation (SIV) visits. Focus heavily on the operational logistics unique to our trial: apheresis scheduling, collection cycles, conditioning, and infusion coordination.Systems & CRO Oversight (Replacing "Admin Retainer")A frictionless EDC architecture and held-to-account CRO vendors.Proactively identify logic errors or missing fields in the Medidata build (e.g., forms failing to auto-populate) and force the CRO/Data Management to execute formal migrations/fixes.Administrative overhead is not a billable existence; it is the proactive management of systems to reduce friction for the sites and the sponsor.Visit Lifecycle ManagementPredictable, unit-complete monitoring cycles.Own the end-to-end "Visit Unit - from pre-visit preparation and system checks, to execution, query generation, and final trip report delivery-without requiring separate administrative bloat.Key areas of activity:Onsite Monitoring Visit (IMV)Remote Monitoring Visit (RMV) - Data Review, Query Generation, and ReportingSite Initiation Visit (SIV) - prep/trainingPre-Study Visit (PSSV)
Clinical Data and Monitoring Lead in south san francisco at Unknown Company
This position is listed as full time and able to be worked remotely.