Laboratory Project Services Coordinator at IQVIA

Buenos Aires, , Argentina -

Full Time

Start Date

Immediate

Expiry Date

30 Aug, 26

Salary

0.0

Posted On

01 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Coordination, Clinical Trial Operations, Study Startup, Client Communication, Risk Mitigation, MS Office, Excel, English Proficiency, Time Management, Stakeholder Management, Documentation, Quality Standards

Industry

Hospitals and Health Care

Description

We are seeking Laboratory Project Services Coordinator to join IQVIA Laboratories at Buenos Aires. 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. Job Summary: Under general direction, manage laboratory-related aspects of clinical trial projects for a client or client program, supporting project delivery from startup through closeout. You will partner closely with the Project Manager and cross-functional teams to keep work on track, communicate progress, and help ensure high-quality execution across multiple studies. What You'll Be Doing: Support the Project Manager with study initiation activities, including required documentation, coordination, and readiness tracking Coordinate day-to-day laboratory project activities to support delivery of agreed timelines, milestones, and client expectations Serve as a key point of contact for assigned clients after study award, maintaining clear and timely communications throughout the study lifecycle Monitor project status, identify risks or blockers, and escalate appropriately with proposed mitigation actions Manage multiple priorities across mid-size and large pharma accounts, balancing urgency and accuracy under pressure Leverage internal team members and stakeholders to resolve issues, align on next steps, and keep deliverables moving Maintain organized project records and ensure adherence to applicable procedures, quality standards, and study requirements What We Are Looking For: Bachelor’s degree in any discipline Experience supporting clinical trial or laboratory operations projects, including study startup and ongoing coordination activities Proficiency with project tracking and documentation tools (e.g., MS Office/Excel, project trackers) and comfort working in structured processes Proficiency in English Other Equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role: Highly organized with strong attention to detail and the ability to manage competing priorities and deadlines Effective written and verbal communication skills with confidence interacting with clients and internal teams Ability to work calmly and efficiently in a fast-paced environment, proactively identifying issues and driving to resolution Collaborative mindset with demonstrated ability to coordinate across teams and unblock work through influence and follow-through 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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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Responsibilities

Manage laboratory-related aspects of clinical trial projects from startup through closeout. Coordinate day-to-day activities and serve as the primary point of contact for clients to ensure high-quality execution.