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.
The Associate Laboratory Project Set-up Manager leads the design and launch of clinical research studies, ensuring high-quality study start-up deliverables while coordinating effectively with sponsors, CROs, and internal laboratory teams.
- Develop and manage laboratory database design requirements for protocols, amendments, and sponsor-driven changes
- Define and maintain client-specific design standards in alignment with clinical protocols
- Oversee study database configuration and serve as the primary set-up point of contact for internal and external stakeholders
- Collaborate with cross-functional teams including Data Management, Logistics, Clinical Trial Materials, Laboratory Testing, and Specimen Management during project planning
- Maintain and update project documentation including action and issue logs, status reports, and timelines during start-up
- Proactively manage scope changes, identify project risks, and implement contingency plans
- Prepare and present study-specific materials at investigator and kick-off meetings and support audits as required
- Bachelor’s degree in science or a related field
- Experience developing and managing clinical study database configurations and sponsor standards
- Working knowledge of Clinical Trial Management Systems and Microsoft Office applications
- Other Equivalent combination of education, training, and experience may be accepted in lieu of degree
- Strong understanding of clinical research processes, medical terminology, and ICH E6 Good Clinical Practice guidelines
- Excellent organizational, time management, and attention to detail skills in a fast-paced environment
- Proven ability to build effective working relationships with clients, colleagues, and management
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 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.
IQVIABuenos AiresThe Associate Laboratory Project Set-up Manager leads the design and launch of clinical research studies, ensuring high-quality study start-up deliverables……30d+
SovosSan Miguel de TucumánGlobally recognized Training and Development programs. A confident facilitator, equally comfortable in a 5-person huddle or a 30-person webinar.…30d+