Remote Clinical Project Manager for Oncology Trials

Oncology Voice Network LLC

Northern (KY)

Hybrid

USD 105,000 - 165,000

Full time

3 days ago
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Benefits offered by this job

Medical, dental, vision coverage
401(k) match
Tuition reimbursement

Job summary

Theradex Systems, Inc. is seeking a Clinical Project Manager or Sr Clinical Project Manager for remote USA work. You will oversee global oncology trials from feasibility to closeout, coordinating with sponsors, vendors, and cross-functional teams to ensure ICH/GCP compliance and quality.

The role requires a life sciences degree, 4+ years in clinical research, and strong Excel/MS Office skills. Oncology experience and CRO background are highly valued. Up to 30% travel may be required.

Qualifications

  • BS in life sciences required; MS/PhD preferred.
  • 4+ years of clinical research experience with trial site management.
  • Prior project management experience in CRO/pharma environment preferred (senior level).
  • Experience with oncology trials and/or gene/cell therapies is highly preferred.

Responsibilities

  • Clinical Project Leadership: drive successful execution and provide study team guidance.
  • Study Oversight: monitor enrollment, retention and metrics; strategize recruitment.
  • Risk & Quality Management: identify risks; develop CAPA plans and oversee QA.
  • Compliance & Audits: manage TMF and support internal/external audits.
  • Budget & Timelines: manage study timelines; review invoices and CO activities.
  • Team Management: lead study team activities and trainings.

Skills

Clinical project mgmt
Team leadership
Vendor management
Study oversight
Clinical trial knowledge
Risk assessment
Critical thinking

Education

BS in life sciences
MS/PhD preferred

Tools

Excel
MS Office

Job description

Theradex Systems, Inc. is seeking a Clinical Project Manager or Sr Clinical Project Manager for remote USA work. You will oversee global oncology trials from feasibility to closeout, coordinating with sponsors, vendors, and cross-functional teams to ensure ICH/GCP compliance and quality.

The role requires a life sciences degree, 4+ years in clinical research, and strong Excel/MS Office skills. Oncology experience and CRO background are highly valued. Up to 30% travel may be required.

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