IQVIA Laboratories
drug discovery and development
AssociateProjectManager
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Associate Project Manager at IQVIA Laboratories. Facilitate study setup. Develop project plans”
Industry & Context.
identify potential risks; develop mitigation strategies
What They're Looking For.
Must Have
Knowledge of project management methodologies, processes, and best practice technology, Skill in creating and maintaining project timelines to ensure deadlines are met, Experience in managing project budgets to avoid cost overruns, Ability to achieve results through collaborative efforts with others, Ability to identify potential risks and develop mitigation strategies
Nice to Have
Bachelor’s degree in Life Sciences and/or related field, Minimum of 18 months experience in a project management and customer-facing environment, Over 2 years of experience in the clinical or research industry, Experience in successfully leading large, global, and complex Phase I-IV clinical trials
What You'll Do.
Facilitate study setup
Develop project plans
Partner with Study Setup team
Oversee protocol documentation
Prepare and present materials
Monitor project plans
Oversee study monitoring
Manage study scope changes
Monitor quality of study
Implement changes as required
Coordinates company services
How You'll Work.
Team & Collaboration
Collaborate with project management to improve processes and service quality
Process & Methodology
project management methodologies, project plans, project timelines, project budgets, study scope changes, budget monitor
Full Job Description
**Associate Project Manager** **IQVIA Laboratories** **Home-based, office-based, hybrid options available** IQVIA Laboratories is a global leader in drug discovery and development, offering comprehensive central and specialty biomarker services. Our expertise includes genomics, immunoassays, flow cytometry, anatomic pathology, precision medicine, vaccine assays, ADME, and bioanalytical services. We also specialize in antibody and biomarker discovery and decentralized clinical trial solutions. Committed to scientific rigor and operational excellence, we support all phases of drug development, ensuring high data integrity and accelerating transformative therapies. **Join us on our exciting journey!** **Job Overview:** Facilitate study setup, including protocol and budget review, leading meetings, and developing project plans. Partner with the Study Setup team for quality database setup and oversee protocol documentation. Prepare and present protocol-specific materials at Kick Off and Investigator meetings. Monitor project plans, timelines, and deliverables, manage documentation, and oversee study monitoring and reporting. Manage study scope changes and budget monitor quality of the study and any service-related issues, implementing changes as required. Collaborate with project management to improve processes and service quality. Coordinates company services, such as but not limited to, database setup, data management, and lab operations, and serves as a resource for internal departments. **Requirements:** * Bachelor’s degree in Life Sciences and/or related field preferred Equivalent combinations of education, training, and experience may be considered. * Knowledge of project management methodologies, processes, and best practice technology. * Minimum of 18 months experience in a project management and customer-facing environment preferred. * Over 2 years of experience in the clinical or research industry preferred. * Skill in creating and maintaining project timelines
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