About The Job:Support global oncology trials across startup, enrollment, and site management phasesWork closely with Clinical Operations leadership to review protocols, informed consents, study plans, and trial documentationDrive vendor and CRO oversight, and help maintain high-quality TMF documentation and regulatory complianceBuild strong relationships with clinical sites and proactively resolve operational hurdlesRequirements:Must have 2-3 years of experience in biotech or pharma supporting industry-sponsored clinical trialsMust have Oncology therapeutic experience at a Biotech or Pharma company.Must be located in CaliforniaThrives in a fast-paced, collaborative biotech environmentElixir Associates are pleased to be partnered with a a clinical-stage biotech company that's developing breakthrough oncology therapies. Having recently received highly positive clinical data, they are now expanding their clinical operations team as they move further into their pivotal trials.They’re looking to hire a Senior Clinical Trial Management Associate to support both early and late-stage studies across multiple programs.The Company offers a very attractive Base Salary, Bonus, Healthcare and Stock Options.If this opportunity is of interest to you or you would like to find out more, please reach out to me over LinkedIn or to dan.spencer@elixir-associates.com

Senior Clinical Trial Management Associate

Emma

Requirements and responsibilities

Skills wanted:

Language(s) required:

Admin access needed