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Associate Laboratory Project Services Manager (REMOTE)

Key Facts

Remote From: 
Category:  Project Manager
Full time
Mid-level (2-5 years)
English

Other Skills

  • •
    Data Reporting
  • •
    Microsoft Office
  • •
    Project Design
  • •
    Social Skills
  • •
    Time Management
  • •
    Detail Oriented

Roles & Responsibilities

  • Bachelor's Degree in Life Sciences and/or related field preferred
  • 2+ years of clinical or research industry experience, including 1 year project management / project set up experience
  • Working knowledge of central laboratory operations including logistics, specimen management, and data reporting
  • Proficiency in Microsoft Office and experience with centralized laboratory or project management systems

Requirements:

  • Manage all laboratory aspects of clinical trial projects, serving as the main point of contact for customers throughout the study lifecycle
  • Lead study setup activities including protocol and budget review, project planning, and risk and issue tracking
  • Monitor project timelines, deliverables, and documentation across the full study lifecycle including eTMF management
  • Act as the primary customer contact, building strong relationships and facilitating clear communication

Job description

We are seeking Associate Laboratory Project Services Manager to join IQVIA Laboratories at Marietta, GA remotely.

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, serving as the main point of contact for customers throughout the study lifecycle. Ensure studies are delivered in alignment with standard operating procedures, policies, and best practices.
 

What You'll Be Doing:

  • Lead study setup activities including protocol and budget review, project planning, and risk and issue tracking
  • Coordinate with study setup teams to ensure quality database configuration and protocol-specific documentation
  • Monitor project timelines, deliverables, and documentation across the full study lifecycle including eTMF management
  • Manage study scope changes, budgets, and service quality while implementing improvements as needed
  • Act as the primary customer contact, building strong relationships and facilitating clear communication
  • Coordinate and resolve study-level issues, acting as an escalation point when required
  • Represent the company at investigator meetings, audits, and training sessions for sites and stakeholders
  • Support continuous improvement initiatives and assist in training less experienced team members
     

What We Are Looking For:

  • Bachelor's Degree in Life Sciences and/or related field preferred
  • 2+ years of clinical or research industry experience, including 1 year project management / project set up experience Pref Or Equivalent combination of education, training and experience
  • Working knowledge of central laboratory operations including logistics, specimen management, and data reporting
  • Proficiency in Microsoft Office and experience with centralized laboratory or project management systems
  • Other Equivalent combination of education, training, and experience may be accepted in lieu of degree
     

The Knowledge, Skills and Abilities Needed for This Role:

  • Strong interpersonal and customer relationship management skills
  • Ability to manage multiple priorities in a fast-paced environment while meeting deadlines
  • Effective written and verbal communication skills with strong attention to detail
     

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 https://jobs.iqvia.com/benefits.
 
If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!

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. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. 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. https://jobs.iqvia.com/eoe

IQVIA 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.

The potential base pay range for this role, when annualized, is $64,200.00 - $133,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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