Associate Project Services Manager

Description

Summary: The Project Manager leads central laboratory clinical trial projects from set-up through closeout, ensuring delivery against scope, timeline, budget, and quality expectations while serving as the primary client liaison. Highlights: 1. Lead assigned clinical trial laboratory projects from award through closeout 2. Serve as the primary point of contact for sponsors 3. Coordinate cross-functional teams to mitigate study risks Buenos Aires, Argentina \| Full time \| Home\-based \| R1535205 ### **We are seeking a Project Manager to join IQVIA Laboratories in Argentina.** 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:** ---------------- The Project Manager is responsible for leading assigned central laboratory clinical trial projects from study set‑up through closeout, ensuring delivery against scope, timeline, budget, and quality expectations while serving as the primary client liaison.**What You'll Be Doing:** ------------------------- * Manage assigned clinical trial laboratory projects from award through study closeout * Lead seamless study set‑up by reviewing protocols, bids, budgets, and ensuring alignment with laboratory design and processes * Develop and maintain project management, communication, risk management, and cost containment plans * Monitor timelines, milestones, scope, and budget, implementing corrective actions as required * Serve as the primary point of contact for sponsors, leading client meetings and issue resolution * Oversee development and maintenance of protocol‑specific laboratory documentation and specifications * Coordinate cross‑functional teams to proactively identify and mitigate study risks **What We Are Looking For:** ---------------------------- * Bachelor’s degree in Life Sciences or a related field, or equivalent relevant experience * 3–5 years of experience in clinical trials, hospital‑funded research, project management, or a laboratory environment * Working knowledge of central laboratory operations including logistics, kits and supplies, specimen management, and data reporting * Demonstrated proficiency with Microsoft Office and laboratory or project management systems * Other equivalent combinations of education, training, and experience may be accepted in lieu of degree **The Knowledge, Skills and Abilities Needed for This Role:** ------------------------------------------------------------- * Strong client management, interpersonal, and stakeholder communication skills * Ability to manage multiple priorities in a fast‑paced environment while meeting deadlines * Excellent written and verbal communication skills in English * Proven ability to build effective working relationships across cross‑functional teams **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.