Clinical Trial Associate
Kura OncologyPrecision Oncology company
Boston, United States$87,266 - $102,000Mid
EcoR1
Operations & Strategy
About the role
TL;DR
Supports clinical trial operations from start-up to close-out, ensuring efficiency and compliance.
- •The Clinical Trial Associate (CTA) supports the operational execution of clinical trials from start-up through close-out.
- •This role partners closely with Clinical Trial Leaders, study teams, CROs, and vendors to ensure trials are conducted efficiently, compliantly, and in alignment with program and company objectives.
- •Key Responsibilities Support clinical trial operations across all phases of the study lifecycle.
- •Assist with CRO and vendor coordination and oversight.
- •Collect, track, and review investigator site regulatory documentation.
- •Manage Trial Master File (TMF) filing, maintenance, and reconciliation.
- •Track and maintain essential study documentation, including CTA and budget status, site and vendor payments, and enrollment metrics.
- •Requirements Bachelor's degree in a scientific field with 1-2 years of professional experience in a clinical research-related position.
- •Familiarity with ICH-GCP and current FDA regulations.
- •Experience with using different eTMF systems (e.g., Veeva Vault).
- •Strong computer skills including MS Office (Excel, Word, PowerPoint), Outlook, and TEAMS.
- •Ability to travel based on assigned study needs (typically minimal).
Required skills
ExcelPowerPointProject Management
Domain expertise
biotechhealthcare
Benefits & perks
equity, annual target bonus, 401K + Employer contributions, Generous stock options, ESPP Plan, 20 days of PTO, 18 Holidays, Generous Benefits Package, Paid Paternity/Maternity Leave, In-Office Catered lunches, Home Office Setup, Lifestyle Spending Stipend, Commuter Stipend
Tech stack
ExcelPowerPoint