Lab Associate

Job Overview
The position focuses on the execution of clearly defined, remote‑capable activities for Anatomic pathology lab operations (dry lab role).

Essential Functions
    • Pending list (PL) management: 
        ○ As a core operational activity to ensure timely case progression, turnaround time adherence, and proactive risk mitigation. 
        ○ Monitor case status daily, identify potential delays, and drive timely resolution through structured follow‑ups and escalation where required.
    • Query management: 
        ○ Prioritizing responses in conjunction with pending list status. 
        ○ Coordinate closely with Project Management, laboratory teams, and stakeholders to ensure queries are addressed accurately and within defined timelines.
    • Study/Sponsor-specific support: 
        ○ Provide sponsor‑specific and study‑level management for region specific activities.
        ○ Perform manual aggregation of results for sponsor studies to enable pathologist summary review, ensuring data completeness, accuracy, and consistency
        ○ Support delivery of revenue‑generating programs by meeting sponsor‑specific expectations and timelines.
    • Conduct assay reviews to ensure documentation alignment, regulatory readiness, and compliance with applicable requirements.
    • Support SOP lifecycle management, including review, updates, and implementation of process changes relevant to offshore regional operations.
    • Perform report reviews, ensuring data integrity, accuracy, and readiness for downstream review and release.
    • Maintain and update processing-specific trackers to ensure accurate workflow monitoring.
    • Assist in drafting and developing new laboratory procedures, techniques, and support writing reports.
    • Communicate clearly, accurately, and promptly with cross-functional stakeholders.
    • Engage in continuous learning through self-study, in-service training, lectures, and meetings.
    • Promote and adhere to safety, quality, and 6S initiatives.
    • Ensure compliance with company procedures and all applicable regulatory requirements.

Qualifications
    • Education: Bachelor’s degree in Medical Laboratory Technology, or a related Life Science field (required).
    • Experience: Minimum 6 months of relevant laboratory experience or an equivalent combination of education, training, and experience (required).
    • Knowledge & Skills: 
        ○ Basic understanding of laboratory principles and Good Laboratory Practices (GLP).
        ○ Familiarity with regulatory standards and laboratory safety protocols
        ○ Knowledge of laboratory equipment, instrumentation, and terminology relevant to the role.
        ○ Proficiency in basic computer applications.
        ○ Ability to maintain effective reporting systems and manage workflow.
        ○ Strong collaboration skills for working with internal stakeholders.
    • Certifications: Applicable licenses and certifications as mandated by local, state, or national regulatory bodies (required).

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.