Associate Project Manager Jobs

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About The Position

IQVIA Laboratories is seeking experienced laboratory professionals to join its Project Services team. This role is 100% remote and follows Pacific Time business hours. Hiring is at multiple levels, with candidates aligned to the appropriate level based on experience. Under general direction, the role manages all laboratory aspects of clinical trial projects for a client or specific program. It serves as the primary point of contact from award through start-up, maintenance, and closeout, leading planning, communication, risk management, and cross-functional coordination to deliver high-quality, customer-focused execution. The annualized potential base pay range is $64,200 to $173,000. Actual base pay may vary based on job-related qualifications, location, and schedule. Depending on the position, incentive plans, bonuses, and other compensation or benefits may also be offered. IQVIA describes itself as an equal opportunity employer and states that it maintains a zero-tolerance policy for candidate fraud.

Requirements

  • At least 3 years of experience in a regulated laboratory environment.
  • At least 2 years of experience managing projects, such as study setup, method validation or transfer, or client programs; a formal project management title is not required.
  • Computer proficiency with Microsoft Office (Word, Excel, and PowerPoint) and comparable company systems in a project delivery environment.
  • Strong interpersonal and client management skills, including the ability to interact effectively with sponsor stakeholders.
  • Experience with Lab Trial Management Systems (LTMS).
  • Strong organizational skills, accuracy, and attention to detail while managing multiple priorities and deadlines.
  • Strong written and verbal communication skills, good command of English, and familiarity with clinical research terminology.
  • Ability to work effectively in a fast-paced, high-stress environment with a customer-focused mindset.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

Nice To Haves

  • Bachelor's degree in Life Sciences and/or a related field is preferred.

Responsibilities

  • Manage assigned clinical trial laboratory projects from award through closeout, ensuring protocol requirements are understood and applied.
  • Lead study setup, including protocol and budget review, startup 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; lead client communications and meetings, and triage and escalate issues.
  • 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.

Benefits

  • The company offers integrated benefits and resources addressing employees' physical, mental, emotional, financial, and social well-being; specific benefit offerings are not detailed in the posting.
  • Depending on the position, incentive plans, bonuses, and other forms of compensation may be offered.
  • The posting refers applicants to the company's benefits website for more information.

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