Science & Technology · Permanent
Associate Manager / Manager, Project Services - Laboratories (Remote - East Coast)
IQVIA · New York, United States
- Location: New York, United States
- Employment: Permanent
Job description
<b>Overview</b> <p>In this remote role, you manage laboratory aspects of clinical trial projects from award through closeout, acting as the primary contact for sponsors. You will lead planning, risk management, and cross-functional coordination to ensure compliant, high-quality execution. You collaborate with sponsors and internal teams to address obstacles and maintain focus on delivery and customer satisfaction. This position supports transforming and accelerating R&D, contributing to impactful patient outcomes.</p> <b>Compensation / Benefits</b><ul><li>integrated benefits programs</li><li>health and welfare benefits</li><li>well-being support</li><li>financial and social well-being resources</li><li>employee-centric approach</li><li>career development opportunities</li></ul> <b>Responsibilities</b><ul><li>Manage clinical trial laboratory projects from award through closeout; ensure protocol requirements are understood and applied</li><li>Lead study setup activities, including protocol and budget review, start-up meetings, and risk management planning</li><li>Monitor timelines, deliverables, metrics, budgets, and handle scope changes and change orders</li><li>Act as the single point of contact for sponsors; lead communications, meetings, and issue triage/escalation</li><li>Coordinate cross-functional resources for timely, customer-focused problem solving</li><li>Oversee development of protocol-specific laboratory documentation and maintenance of laboratory specifications</li><li>Support proposal development, bid defense, and creation of sponsor/program-specific standards and procedures</li><li>Capture lessons learned and drive continuous improvement across projects</li></ul> <b>Key requirements</b><ul><li>Bachelor's Degree in Life Sciences and/or related field (preferred)</li><li>3+ years in a regulated laboratory environment</li><li>2+ years of project management experience (not necessarily with formal PM title)</li><li>Proficiency with Microsoft Office and project delivery systems</li></ul><ul><li>Strong interpersonal and client management skills</li><li>Excellent written and verbal communication in English</li><li>High attention to detail and ability to manage multiple priorities</li><li>Lab Trial Management Systems (LTMS)</li><li>Microsoft Office (Word, Excel, PowerPoint)</li><li>Clinical research terminology</li></ul><img src="https://www.jobg8.com/Tracking.aspx?e6alHVjzw7%2fkmKOPcUamO18ZsV6gzWD9d" width="0" height="0" />