Jobs at The START Center for Cancer Research

Provides enterprise leadership for pharmacy operations across START’s U.S. clinical research sites. Responsibilities include standardizing investigational drug services, sterile compounding, clinical documentation, procurement, compliance, quality systems, KPIs, technology strategy, audits, and site launches. The role develops pharmacy leaders, manages budgets and change initiatives, ensures regulatory and GCP readiness, and serves as a subject-matter expert in investigational drug management for early-phase oncology trials.

Maintains Investigator Site Files and regulatory documents for oncology clinical trials. Responsibilities include processing IRB submissions, safety reports, monitor visits, study staff logs, training records, investigator signatures, CVs, licenses, laboratory certifications, and study archiving. The role also tracks CITI training, manages revised study documents, updates databases and task lists, and performs quality assurance checks. This is a remote Monday–Friday position requiring strong organization, attention to detail, proofreading, and proficiency with Microsoft Word.

Prepare and submit regulatory documents (IRB, FDA, IBC) for oncology clinical studies, draft informed consents, maintain Investigator Site Files, act as point of contact with Sponsors/CROs and regulatory bodies, track activities in regulatory systems, and respond to inquiries and status requests.

Research and map clinical research financials from CTMS reports, reconcile site expenses, support sponsor/CRO invoicing, collaborate with accounting and clinical teams, and improve mapping and reconciliation processes to ensure accurate sponsor billing and revenue capture.