Associate BioServices Project Manager - Hybrid

Q² Solutions; Indianapolis (IN); Hybrid; USD 62,000 - 129,100; Full time

Job summary

A global research service provider is seeking an Associate BioServices Project Manager in a hybrid role based in Indianapolis, IN. The candidate will oversee the lifecycle of projects, collaborating with scientific and technical teams to ensure timely completion and compliance with regulatory standards. Required qualifications include a Bachelor's degree in a scientific field and 3 years of experience in an ADME laboratory. Strong skills in liquid chromatography, mass spectrometry, and attention to detail are essential for success in this role. The role offers a pay range of $62,000 to $129,100 annually.

Qualifications

• 3 years of related experience in an ADME laboratory environment.
• Understanding of liquid chromatography combined with mass spectrometry.
• Experience in sample extraction and routine laboratory procedures.

Responsibilities

• Oversee and conduct projects throughout their lifecycle.
• Collaborate with scientific teams to ensure timely project completion.
• Maintain communication with customers, providing updates on projects.

Skills

Liquid chromatography

Mass spectrometry

Sample extraction

Method development

Team collaboration

Attention to detail

Effective communication

Education

Bachelor's Degree in a scientific field

Job description

Join to apply for the Associate BioServices Project Manager - Hybrid role at Q² Solutions.

We are seeking an Associate BioServices Project Manager to join IQVIA Laboratories in Indianapolis, IN - hybrid. 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.

What You’ll Be Doing

• Overseeing and conducting projects throughout their lifecycle, including method development, validation, and sample analysis.
• Collaborating with Scientific Team Members, Technical Writing, and QC to ensure timely project completion.
• Reviewing validation and bioanalytical reports for completeness.
• Maintaining communication with customers, providing daily updates on active projects.
• Resolving sample discrepancies and monitoring project progress.
• Providing regular project status updates to management.
• Preparing validation and sample analysis plans.
• Reviewing data for scientific quality.
• Coordinating and visiting customer sites.
• Working with business development staff to prepare quotes for assigned customers.
• Approving validation experimental designs and preparing data for external presentations.
• Ensuring projects are archived in accordance with IQVIA SOPs.
• Complying with all applicable regulatory standards, including Good Clinical and Good Laboratory Practices.

What We Are Looking For

• Bachelor's Degree in a scientific field.
• 3 years of related experience in an ADME laboratory environment.
• Understanding of liquid chromatography combined with mass spectrometry.
• Experience in sample extraction and routine laboratory procedures.
• Understanding of method development and validation of assays.
• Other equivalent combination of education, training, and experience may be accepted in lieu of a degree.

The Knowledge, Skills, And Abilities Needed For This Role

• Collaborative skills to achieve results through teamwork.
• Proficiency in liquid chromatography and mass spectrometry.
• Expertise in sample extraction and routine laboratory procedures.
• Strong understanding of method development and validation of assays.
• Ability to interact with external and internal clients and work to objectives and timelines.
• Excellent attention to detail and communication skills.
• Ability to follow verbally communicated procedures.
• 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, 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.

The potential base pay range for this role, when annualized, is $62,000.00 - $129,100.00. 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.

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.