Novotech
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Biotech
Supports investigator payment processing and grant development for clinical research studies. Reviews protocols, contracts, visit data, and payment reports; builds site-specific subject visit tracking templates in CTMS; processes and reconciles investigator payments; prepares budgets and estimates; addresses fair market value questions; manages system access and vendor issues; and collaborates with project managers, clinical operations, investigators, and clients while following SOPs and quality requirements.
Biotech
Lead clinical systems, reporting and AI/automation initiatives for clinical operations. Manage end-to-end project delivery, stakeholder governance, KPI/reporting definition (Power BI/Excel), and drive adoption, compliance and process improvements across Veeva/Obvio and eClinical platforms.
Biotech
Supports the Clinical Lead in overseeing clinical research project delivery, performance, timelines, risks, quality, compliance, and site-level communications. Provides analytics, reports, KPI reviews, risk alerts, mitigation recommendations, and action-item follow-up. Monitors site performance, protocol adherence, study quality, clinical databases, and protocol deviations while supporting project execution and regulatory compliance throughout study start-up, maintenance, and closeout.
