Senior Clinical Study Associate
$80 - $85 per hourTundra Technical Solutions
Tundra Technical Solutions provided pay range This range is provided by Tundra Technical Solutions. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $80.00/hr - $85.00/hr Direct message the job poster from Tundra Technical Solutions Senior Clinical Study Associate III Location: Remote or Hybrid (U.S.) Category: Clinical Operations We’re seeking an experienced Senior Clinical Study Associate III to support global clinical trial execution and ensure high-quality operational oversight across study sites. This role is best suited for candidates with pharma-side experience (not CRO-only backgrounds) and strong skills in document review and presentation. What You’ll Do Support day-to-day clinical trial operations, including global site start-up, enrollment tracking, monitoring, and data flow. Prepare and review key study documents (e.g., informed consent forms, site instructions, study manuals, pharmacy binders). Ensure accurate tracking and timely filing of essential documents in the TMF; review site documents for completeness and accuracy. Track patient status and oversee key activities such as sample collection, lab reporting, and testing schedules. Liaise with clinical sites, central labs, vendors, and CRO partners to ensure proper sample handling and timely results. Review monitoring trip reports, track data queries, site metrics, and overall site performance. Participate in a limited number of site initiation, routine monitoring, and close-out visits; co-monitor as needed. Support investigator/vendor meetings and may present content. Contribute to study feasibility assessments and review site contracts and budgets. Coordinate third-party vendor activities including metrics, accruals, and operational planning. What We’re Looking For 3–5 years of clinical research or clinical operations experience , with pharma industry experience strongly preferred . Experience supporting global clinical trials . Strong experience reviewing study documents, especially informed consent forms and operational materials. Excellent presentation, verbal, and written communication skills. Working knowledge of GCP and familiarity with clinical study phases. Proficiency in Word, Excel, PowerPoint, and database-related applications. Highly organized, detail-oriented, and strong at managing multiple priorities. Education Bachelor’s degree or higher in a relevant scientific, healthcare, or technical field. If you’re a collaborative, detail-oriented clinical operations professional ready for a fast-paced and impactful role, we encourage you to apply. #J-18808-Ljbffr Tundra Technical Solutions
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