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Job Summary:
Support the setup, configuration, and validation of laboratory databases within Clinical Trial Management Systems, ensuring quality and compliance with study protocols and regulatory standards. This role is ideal for candidates with foundational clinical research knowledge who are looking to grow into sponsor-facing responsibilities and more complex project ownership.
What You'll Be Doing:
- Configure and support laboratory databases using LIMS/CTMS platforms, ensuring alignment with study protocols and sponsor requirements
- Assist with study validation and perform low-complexity updates, building toward ownership of more complex setup activities over time
- Collaborate with cross-functional teams to ensure smooth project setup and timely delivery
- Maintain accurate documentation and proactively communicate risks, issues, and timeline impacts
- Participate in project planning, including timelines, regulatory checkpoints, and issue identification
What We Are Looking For:
- High School Diploma or equivalent required; Bachelor's Degree in Life Sciences or related field preferred
- Minimum 1 year relevant experience in the Clinical, Medical or Healthcare industry.
- Experience working with Clinical Trial Management Systems (CTMS), LIMS, or similar laboratory database tools
- Basic understanding of clinical research processes, including protocol review and study setup
- 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 organizational skills and attention to detail, with ability to manage multiple priorities in a fast-paced environment
- Ability to work effectively with cross-functional teams and progressively engage with sponsors and stakeholders
- Interest in innovation, including exposure to AI-enabled tools and process improvement initiatives
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 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.