Novotech Benefits Overview

Lead and manage oncology clinical trial projects from site selection through closeout. Oversee timelines, budgets, vendors, regulatory/ethics submissions, patient recruitment, safety coordination, eTMF/CTMS maintenance, and ensure compliance with ICH‑GCP, SOPs and Project Agreements.

Manages Data Management staff, resource allocation, recruitment, onboarding, performance, and professional development. Provides expert oversight of clinical data management deliverables, technical solutions, process improvements, system validation, project budgets, timelines, quality, audits, proposals, and sponsor interactions. Leads biometrics support activities, training initiatives, cross-functional collaboration, and bid defenses while ensuring clinical studies comply with GCP, regulatory requirements, SOPs, and project agreements.

Supports clinical business development by identifying laboratory opportunities in client RFPs, positioning lab services, developing proposals and budgets, presenting bids, and managing follow-up through deal completion. The role coordinates with clinical BD, laboratory operations, proposal teams, and clients; maintains strategic client relationships, monitors satisfaction, tracks sales activity in Salesforce, analyzes competition, and supports laboratory business growth. At least 30% travel is required.