Clinical Data and Site Operator - South San Francisco

Only for registered members South San Francisco, United States

1 day ago

Default job background
Role: · This 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 ...
Job description

Role:
This 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 Detection
Synthesized 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 Management
Predictable, 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 Reporting
Site Initiation Visit (SIV) - prep/training
Pre-Study Visit (PSSV)


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