Clinical Project Manager

October 11

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TFS HealthScience

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CRO • clinical trials • Scientific and Medical consulting • Contract Placement Solutions (staffing) • Regulatory Consulting

501 - 1000

Description

• Overall responsibility for managing projects in accordance with company policies, SOPs, regulatory requirements, financial and contractual obligations • Ensure that projects are delivered on-time, within scope and within budget and in compliance with applicable quality standards • Manages the strategic aspects of projects, identify, analyze and minimize/mitigate risks • Communicates effectively with clients to manage the relationship and evaluate business solutions • 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 • Implements and maintains sound business practices • Measure and evaluate project performance • Manage the project budget, profitability and ensure invoicing is performed on time • Work with Finance & Accounting team to analyze profitability, revenue, margins and utilization • Manage resource allocation on the project in collaboration with respective line managers • Facilitate internal and external communication • Report and escalate to management as needed • Establish and maintain relationship with third parties/vendors • Manage high-level deliverables across the organization • Participate in capability presentations/bid defenses as needed • Continually define ways to increase customer satisfaction and deepen client relationships • Contribute in review/develop procedures, guidelines, SOPs, metrics as needed

Requirements

• Over 5 years of experience, preferably in early-stage oncology development • 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 • Preference for candidates with experience working in small, fast-paced biotech companies • Native Spanish speaker is required, with a good command of English • Flexibility to work remotely or in a hybrid model • Proactive, mature in clinical operations, and passionate about working in early-stage drug development

Benefits

• Competitive compensation package • Comprehensive benefits • Opportunity for personal and professional growth