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Our client, a cutting-edge biopharmaceutical company, is seeking an experienced Senior Clinical Trial Manager (Sr. CTM) to join their Clinical Operations team.
Responsibilities:
Lead global Phase II clinical trials, ensuring compliance with ICH/GCP and regulatory requirements.
Manage CROs, sites, and vendors to maintain quality, timelines, and budgets.
Develop and review critical study documents and processes.
Track progress, mitigate risks, and ensure timely issue resolution.
Requirements:
7+ years of clinical operations experience in biotech/pharma.
Strong background in Phase II global studies, with 3+ years of trial management experience.
Expertise in vendor and budget management.
Knowledge of regulatory guidelines (FDA, EU, ICH/GCP).
Location & Compensation:
Remote: Must Live in PST Time zone
Pay rate $90-110/hr (approx. $187k-228k per year)
Apply Now to be Considered!
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Strategy/Planning, Project Management, and Management
Industries
Biotechnology Research and Pharmaceutical Manufacturing
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