Senior Clinical Trial Operations Lead (Hybrid)

ACTalent

United States

Hybrid

USD 48,000 - 52,000

Full time

4 days ago
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Benefits offered by this job

Medical, dental & vision
401(k) Retirement Plan
Life Insurance (Voluntary)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick)

Job summary

Actalent is seeking a Clinical Trial Associate to support the planning, execution, and closeout of 3-4 clinical programs, alleviating administrative workload from the Clinical Trial Manager and enabling growth as bandwidth allows.

The role requires onsite presence two times per week in Lexington, MA, offering a pathway into sponsor-side operations and exposure to CROs, vendors, and study sites. The position pays $35.00-$38.00/hr with potential benefits for eligible contractors.

Qualifications

  • Demonstrated ability to independently manage standard CTA responsibilities.
  • Strong organization, prioritization, follow-up, and attention to detail across multiple studies.
  • Ability to identify next steps, connect information across workstreams, and follow through on actions.
  • Working knowledge of ICH-GCP and clinical trial documentation/TMF expectations.
  • Strong communication with CROs, sites, vendors, and cross-functional stakeholders.

Responsibilities

  • Support study planning, execution, and closeout activities across 3-4 programs.
  • Manage eTMF/TMF review and maintenance, ensuring timely filing and quality follow-up.
  • Coordinate day-to-day activities with CRO, sites, vendors, and internal study stakeholders.
  • Assist Clinical Trial Managers with site management, monitoring report review, and study documentation.
  • Support contracts, vendor coordination, budgets/invoices, CTMS, and clinicaltrials.gov updates.
  • Capture meeting minutes/action items and follow through on outstanding activities.

Skills

CTA responsibilities
Organization & prioritization
Cross-functional communication
ICH-GCP knowledge
Stakeholder coordination

Education

Bachelor's degree

Tools

CTMS/eTMF

Job description

Actalent is seeking a Clinical Trial Associate to support the planning, execution, and closeout of 3-4 clinical programs, alleviating administrative workload from the Clinical Trial Manager and enabling growth as bandwidth allows.

The role requires onsite presence two times per week in Lexington, MA, offering a pathway into sponsor-side operations and exposure to CROs, vendors, and study sites. The position pays $35.00-$38.00/hr with potential benefits for eligible contractors.

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