Clinical Team Lead

🔥 7 minutes ago

🌐 Mexico, Chile, +2 more countries – Remote

🇲🇽 Mexico – Remote 🇨🇱 Chile – Remote 🇨🇴 Colombia – Remote 🇵🇪 Peru – Remote

⏰ Full Time

🟠 Senior

✨ Team Lead

👻 Ghost score 10%

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Fortrea

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.

📋 Description

• Own clinical delivery of clinical research trials as the Clinical Project Manager within the core project team • Partner with the Project Manager and functional leads to deliver clinical trial aspects within contractual and budgetary requirements • Oversee clinical and site management aspects of trials and represent clinical delivery to customers • Drive clinical project performance toward contracted deliverables and customer needs • Lead communication and collaboration with clients and multicultural project teams • Develop clinical project strategy and prioritize scope, timelines, quality, and budget • Prepare and deliver presentations for new business as required • Manage subject recruitment and retention, clinical vendor delivery, and monitoring visit strategy • Identify clinical, financial, and quality risks using risk management and quality-by-design principles • Use data sources, dashboards, and risk management strategies for proactive problem solving • Maintain project governance, escalation pathways, clinical project plans, SOP, client, and regulatory compliance • Manage project budgets, resources, scope, revenue forecasts, costs, and financial milestones • Lead scope changes and change-order processes and track client-specific KPIs • Build high-performing clinical project teams and facilitate communication and teamwork • Ensure accurate clinical resource projections and escalate resource constraints • Develop and mentor team members and provide feedback to line managers • Oversee regulatory/ethics committee submissions, tracking, and documentation • Participate in Bid Defense preparation and meetings as required • Perform other assigned duties

🎯 Requirements

• University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution • Relevant and equivalent experience may be considered in lieu of educational requirements • Fluent in English, both written and verbal • 2+ years clinical research/monitoring experience or equivalent combination of education and experience • Working knowledge of ICH Guidelines and GCP, including international regulatory requirements • Advanced computer skills, including Microsoft Word, Excel, Project, Access, and PowerPoint • Experience managing projects in a matrix and virtual environment • Excellent communication, planning, and organizational skills • Ability to lead by example and encourage independent problem-solving • Ability to handle multiple competing priorities and use resources effectively • Ability to inspire teamwork and motivate staff within a matrix system • Financial awareness and ability to use financial tracking systems • Ability to work independently and mentor junior project team members • Ability to negotiate and liaise with clients professionally • Ability to present to staff at all levels • Preferred: Master or other advanced degree • Preferred: PMP certification • Preferred: 2+ years CRA experience, on-site or in-house • Candidates with three or more years of relevant clinical research experience in pharmaceutical, CRO, or healthcare settings may be considered in lieu of the stated minimum requirement

🏖️ Benefits

• Remote-based work option • Weekend and off-hour work as required • Travel opportunities/requirements up to 30% (global—primary domestic and international)

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