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Senior Clinical Trial Associate

Job in Elizabeth, Union County, New Jersey, 07215, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-09-22
Job specializations:
  • Healthcare
    Clinical Research, Healthcare Compliance
Salary/Wage Range or Industry Benchmark: 90000 - 120000 USD Yearly USD 90000.00 120000.00 YEAR
Job Description & How to Apply Below

Role Overview

Senior Clinical Trial Associate (Sr. CTA) on the Clinical Operations team to support early-stage clinical development, executing complex Phase I/II CAR-T oncology trials with operational, administrative, and coordination support.

Key Responsibilities
  • Provide cross-functional administrative and operational support for study team meetings, advisory boards, investigator meetings, and other study forums.
  • Support Senior Clinical Trial Managers with day-to-day execution of Phase I/II CAR-T oncology trials in compliance with ICH-GCP and applicable regulations.
  • Oversee preparation, organization, and maintenance of trial documentation (regulatory files, TMFs/eTMFs, correspondence); ensure documents are current, complete, and compliant with ICH-GCP and company SOPs.
  • Assist with trial planning, start-up, execution, and close-out; coordinate with sites and support protocol/regulatory compliance.
  • Prepare, submit, and track regulatory and IRB/IEC documents; maintain knowledge of applicable regulations and standards.
  • Schedule/coordinate meetings (investigator meetings, site visits, internal meetings); prepare agendas, minutes, track action items.
  • Track trial progress (site activation, enrollment, monitoring, milestones) and maintain status reports/trackers.
  • Support data management (query tracking and data reconciliation) with Data Management.
  • Liaison among clinical team, vendors, CROs, and investigational sites; support vendor oversight.
  • Identify operational issues/risks, propose solutions, and elevate as appropriate; improve processes; mentor junior CTAs.
Requirements
  • Bachelor’s degree in life sciences/clinical research or related field.
  • 3–5 years as a Clinical Trial Associate (or similar role).
  • Experience with trial coordination, regulatory documentation, and site management.
  • Oncology trial experience required; cell therapy and/or CAR-T strongly preferred.
  • Strong ICH-GCP/regulatory understanding; proficiency with CTMS, eTMF, and EDC.
  • Excellent organization, communication, problem-solving; ability to work cross-functionally.
  • Proficiency in Microsoft Office; familiarity with eTMF/EDC platforms.
Benefits
  • Benefits are offered exclusively to permanent full-time employees (contractors not eligible).
Work Authorization

Applicants must be authorized to work in the United States; E-Verify and Form I-9 required if hired.

Position Requirements
10+ Years work experience
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