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Clinical Team Lead, FSP - Oncology

Remote / Online - Candidates ideally in
High Point, Guilford County, North Carolina, 27264, USA
Listing for: FTINC Fortrea Inc.
Remote/Work from Home position
Listed on 2026-06-18
Job specializations:
  • Management
    Program / Project Manager, Data Science Manager, Operations Manager
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Job Overview

Fortrea is seeking Oncology Clinical Team Leads (CTLs) to join our FSP team. Candidates should have at least 3 years of monitoring experience and be based in the US or Canada. This role focuses on the clinical delivery of oncology clinical trials.

Responsibilities
  • Own the clinical delivery of clinical research trials and act as the Clinical Project Manager.
  • Partner with the Project Manager and functional leads to ensure successful delivery within contractual and budgetary limits.
  • Oversee clinical and site management aspects, representing clinical delivery to the customer.
  • Drive proactive communication and collaboration with clients and project teams.
  • Lead the development of the clinical project strategy, prioritization, and clear data‑driven strategies.
  • Prepare and deliver presentations for new business as required.
  • Manage operational aspects to support subject recruitment, retention, clinical vendor delivery, and monitoring visit strategy.
  • Identify clinical, financial, and quality risks, using risk‑management practices and dashboards.
  • Adhere to project governance, issue escalation pathways, and regulations including SOPs, client and regulatory requirements.
  • Partner with team members to oversee budgets, resources, and scope adherence.
  • Forecast clinical project revenue, manage costs, and lead change‑order processes.
  • Track and report KPIs and client‑specific metrics.
  • Provide leadership and foster high‑performing clinical project teams.
  • Mentor and provide feedback to team members.
  • Participate in regulatory/ethics committee submissions and documentation.
  • Support new‑business Bid Defense preparation and meetings as needed.
Qualifications (Minimum Required)
  • University/college degree (life science preferred) or a related allied health certification; equivalent experience may be considered.
  • Minimum 5 years of clinical research/monitoring experience with a Bachelor’s degree, or equivalent combination of education and experience.
  • Minimum 3 years of experience leading project teams through study start‑up, conduct, data management, analysis, close‑out, and report writing.
  • Oncology experience as a CTL.
  • Experience overseeing external vendors (e.g., CROs, central labs, call centers, DCT providers).
  • Working knowledge of ICH Guidelines and GCP, including international regulatory requirements.
  • Advanced computer skills (Microsoft Word, Excel, Project, Access, PowerPoint).
  • Experience managing projects in a matrix and virtual environment.
  • Excellent communication, planning and organizational skills.
  • Ability to lead by example, inspire teamwork, and manage competing priorities.
  • Financial awareness and knowledge of financial tracking systems.
  • Ability to work independently, mentor junior team members, negotiate and liaise with clients, and present to staff at all levels.
Preferred Qualifications
  • Master’s or other advanced degree.
  • Device experience.
Compensation

Pay Range: $,000 USD annually.

Physical Demands / Work Environment

Standard office environment or remote work required. Weekend and off‑hour work as required.

Travel Requirements

Up to 30% travel (global – primarily domestic and international).

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