Associate BioServices Study Lead Hybrid

We are seeking an Associate BioServices Study Lead to join IQVIA Laboratories in Ithaca NY- 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.

As an Associate BioServices Study Lead you will be the primary point of contact for our external customers ensuring exceptional customer service and adherence to IQVIA scientific standards.

What youll be doing:

• Providing scientific oversight on projects including method development validation and sample analysis.
• Serving as Principal Investigator for GLP studies.
• Collaborating with Technical Writing and QA to ensure timely project completion.
• Reviewing validation and bioanalytical reports for completeness.
• Maintaining daily communication with customers and providing updates on active projects.
• Resolving sample discrepancies and monitoring project progress.
• Submitting accurate weekly assessments of resource requirements.
• Preparing validation and sample analysis plans.
• Reviewing data for regulatory compliance and scientific quality.
• Conducting thorough investigations of failed runs and organizing method troubleshooting.
• Coordinating and conducting customer visits.
• Working with business development staff to prepare quotes for customers.
• Approving validation experimental designs and preparing data for external presentations.
• Ensuring projects are archived according to Quintiles SOP.
• Complying with all applicable regulatory standards including Good Clinical and Good Laboratory Practices.

What we are looking for:

• Bachelors Degree in a scientific field.
• 3 years of related experience in a GLP laboratory environment.
• Ability to achieve results through collaborative efforts.
• Understanding of liquid chromatography combined with mass spectrometry or in vitro and immunoassay techniques.
• Experience in sample extraction and routine laboratory procedures.
• Understanding of method development and validation of assays.
• Ability to interact with external and internal clients and work to objectives/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.
• 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 collaborative skills.
• Proficiency in liquid chromatography and mass spectrometry.
• Experience in sample extraction and routine laboratory procedures.
• Expertise in method development and validation of assays.

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 youre 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

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. 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.