Senior Clinical Project Lead
hace 2 semanas
Tfs Health Science is a leading global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and functional service (FSP) solutions.
Job Summary:
We are seeking an experienced Senior Clinical Project Lead to manage projects in accordance with company policies, SOPs, regulatory requirements, financial and contractual obligations in early-stage oncology development.
Responsibilities:
* Ensure that projects are delivered on-time, within scope, and within budget in compliance with applicable quality standards
* Manage the strategic aspects of projects, identify, analyze, and minimize/mitigate risks, including technical and operational choices
* Communicate effectively with clients to successfully manage the relationship, identify needs, and evaluate alternative business solutions and strategies
* Develop and maintain project plans and timelines for their project and track progress
* Ensure all study team members are adequately trained on project-specific systems and procedures
* Implement and maintain sound business practices
* Measure and evaluate project performance
* Manage the project budget, profitability, and ensure invoicing is performed on time and in accordance with the scope of work
* Work with the Finance & Accounting team to analyze profitability, revenue, margins, and utilization across their projects
* Manage resource allocation on the project in collaboration with respective line managers
* Facilitate internal and external communication
* Report and escalate to management as needed
Requirements:
* Minimum 5 years of experience in clinical trial management, preferably in early-stage oncology development and within small, dynamic biotechnology companies
* Hands-on experience as a Clinical Research Associate (CRA) combined with study management experience
* Strong background in clinical trial management, including vendor selection, study initiation, execution, monitoring, and closure of clinical studies
* Proven experience in contingency planning and risk management during clinical trials
* Native Spanish speaker required, with good command of English
What We Offer:
Competitive compensation package with estimated annual salary $80,000-$110,000 depending on qualifications and location. Comprehensive benefits and opportunity for personal and professional growth in a rewarding environment.
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