Sr Lab Project Set-Up Coord

Responsibilities

Essential Functions

Technology & AI Enablement

• Lead the design configuration and validation of laboratory databases and study setup activities using advanced Clinical Trial Management Systems (CTMS) and related digital platforms.
• Identify and apply AIenabled tools automation and data analytics to improve study setup efficiency data quality and amendment delivery.
• Partner with technology data and innovation teams to pilot and implement new digital solutions supporting laboratory project delivery.

Innovation & Continuous Improvement

• Actively contribute to innovation initiatives including the evaluation of emerging technologies process automation and intelligent workflows within laboratory operations.
• Challenge existing processes by proposing modern scalable and technologydriven alternatives to traditional project setup models.
• Lead or contribute to lessonslearned sessions translating insights into actionable recommendations and innovation roadmaps.

Project & Amendment Management

• Manage the endtoend design and implementation of protocol amendments and sponsordriven changes ensuring alignment with system capabilities and regulatory requirements.
• Proactively assess the impact of scope changes using datadriven risk identification and mitigation approaches.
• Maintain accountability for the quality accuracy and timeliness of all amendmentrelated deliverables.

CrossFunctional & Stakeholder Collaboration

• Collaborate across Data Management Logistics Clinical Trial Materials Laboratory Testing Specimen Management and Technology teams to align timelines system capabilities and innovation opportunities.
• Communicate effectively with Sponsors and CROs providing expert input on technologyenabled study design and delivery.
• Translate complex technical concepts into clear actionable guidance for internal and external stakeholders.

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

To perform this job successfully an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Knowledge

Requires knowledge of principles theories and concepts of a job area typically obtained through advanced education.

Requires working knowledge of laboratory project setup processes clinical research operations and regulated environments along with familiarity with clinical and laboratory systems digital workflows and compliant ways of working. Demonstrates awareness of emerging technologies automation and AIenabled solutions applying innovative and datadriven thinking to improve laboratory project delivery.

Experience

Typically requires 3 years of prior relevant experience.

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

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.