Associate Project Services Manager - (Clinical Trials and Laboratories)

IQVIA Inc; United States; Remote; USD 90,000 - 130,000; Full time

Job summary

IQVIA Inc seeks experienced laboratory professionals to join the Project Services team at Laboratories. This 100% remote role follows Eastern Time business hours and offers multiple levels aligned to experience.

You will manage all clinical trial laboratory projects from award through start-up, maintenance and closeout, lead startup meetings, monitor timelines and budgets, and act as the primary sponsor contact for issue triage and collaboration.

Qualifications

• Bachelor’s degree in life sciences or related field.
• 3+ years in a regulated lab environment.
• 2+ years managing projects (start-up to closeout) requested.
• Proficiency with MS Office in a project delivery environment.
• English language skills and clinical research terminology.

Responsibilities

• Manage clinical trial lab projects from award to closeout.
• Lead start-up activities, protocol review, and risk plans.
• Monitor timelines, deliverables, metrics, and budgets.
• Serve as main sponsor contact; coordinate meetings and issue triage.
• Drive timely problem solving and cross-functional collaboration.
• Oversee development of protocol-specific lab documents and lab specs maintenance.
• Support proposal development and sponsor standards.

Skills

Project management

Client management

Microsoft Office

Communication skills

Education

Bachelor's Degree in Life Sciences

Tools

LTMS

Job description

Internal Job DescriptionWe are seeking experienced laboratory professionals to join the Project Services team at the company Laboratories.This role is 100% remote (Eastern Time business hours). We are hiring at multiple levels — candidates are aligned to the appropriate level based on experience.

We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.

Job Summary:Under general direction, 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.

What You’ll Be Doing:

• 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

What We Are Looking For:

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

• 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) — a formal project management title is not required

• Demonstrated computer proficiency with Microsoft Office (Word, Excel, PowerPoint) and comparable company systems in a project delivery environment

The Knowledge, Skills and Abilities Needed for This Role:

• Strong interpersonal and client management skills, with the ability to interact effectively with sponsor stakeholders

• Experience with Lab Trial Management Systems (LTMS)

• Strong organizational skills with high accuracy and attention to detail while managing multiple priorities and deadlines

• Strong written and verbal communication skills with good command of English and 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

What We Offer You:

We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees’ physical, mental and emotional, financial and social well‑being so they can thrive at home and at work, at any stage of their well‑being journey.

To learn more about our benefits, visit

If you’re looking to unleash your potential, join the company Laboratories to help make the extraordinary possible!

the company 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. Learn more at

the company is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.