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About the Role

Manage all laboratory aspects of clinical trial projects for a client or a specific program, serving as the primary point of contact from award through start-up, maintenance, and closeout. Lead planning, communication, risk management, and cross-functional coordination to deliver high-quality, customer-focused execution.

Responsibilities

• Manage assigned clinical trial laboratory projects from award through closeout, ensuring protocol requirements are understood and applied
• Lead study set-up activities including protocol and budget review, start-up meetings, and implementation of project and risk management plans
• Monitor timelines, deliverables, metrics, and budgets, including trend analysis, scope changes, and change orders
• Serve as the single point of contact for sponsors, leading client communications, meetings, and issue triage and escalation
• Drive timely, customer-focused problem solving and coordinate cross-functional resources to remove study obstacles
• Oversee development of protocol-specific laboratory instructional documents and maintenance of laboratory specifications
• Support proposal development, bid defense preparation, and development of sponsor or program-specific standards and procedures
• Capture lessons learned and support continuous improvement across projects and programs

Requirements

• 3+ years of experience in a regulated laboratory environment
• 2+ years of experience managing projects (e.g., study setup, method validation or transfer, client programs)
• Demonstrated computer proficiency with Microsoft Office (Word, Excel, PowerPoint) and comparable company systems in a project delivery environment

Skills

• Strong interpersonal and client management skills
• Ability to interact effectively with sponsor stakeholders
• Experience with Lab Trial Management Systems (LTMS)
• Strong organizational skills with high accuracy and attention to detail
• Ability to manage multiple priorities and deadlines
• Strong written and verbal communication skills
• Good command of English and clinical research terminology
• Ability to work effectively in a fast-paced, high-stress environment
• Customer-focused mindset
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients

Location

• Remote

Work Type

• 100% remote
• Pacific Time business hours

Experience Level

• Multiple levels based on experience

Education Level

• Bachelor's Degree in Life Sciences and/or related field preferred

Salary/Compensations

• $64,200.00 - $173,000.00

Benefits

• Integrated benefits programs and resources to take care of employees' physical, mental and emotional, financial and social well-being

About the Company

• IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
• We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
• We create connections that accelerate the development and commercialization of innovative medical treatments.
• Everything we do is part of a journey to improve patient outcomes and population health worldwide.
• To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact.
• No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Equal Opportunity

• All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.