IQVIA

LabAssociate

Mumbai, Maharashtra, India FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“Lab Associate at IQVIA. Skills: Pending list (PL) management, Query management, Study/Sponsor-specific support, Assay reviews, SOP lifecycle management, Report reviews, Cross-functional communication. Pending list (PL) management 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”

What You'll Achieve.

Timely case progression; Turnaround time adherence; Proactive risk mitigation; Queries addressed accurately and within defined timelines; Data completeness, accuracy, and consistency; Meeting sponsor-specific expectations and timelines; Documentation alignment; Regulatory readiness; Compliance with applicable requirements; Data integrity, accuracy, and readiness for downstream review and release; Accurate workflow monitoring

Industry & Context.

Problems you'll solve

Proactive risk mitigation; Identify potential delays, and drive timely resolution through structured follow-ups and escalation

Eligibility Requirements

Adhere to safety, quality, and 6S initiatives, Ensure compliance with company procedures and all applicable regulatory requirements

What They're Looking For.

Must Have

Minimum 6 months of relevant laboratory experience or an equivalent combination of education, training, and experience, 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, collaboration skills for working with internal stakeholders, Applicable licenses and certifications as mandated by local, state, or national regulatory bodies

What You'll Do.

Pending list (PL) management 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

Prioritize query responses in conjunction with pending list status

Coordinate closely with Project Management

and stakeholders to ensure queries are addressed accurately and within defined timelines

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

Support delivery of revenue-generating programs by meeting sponsor-specific expectations and timelines

Conduct assay reviews to ensure documentation alignment

and compliance with applicable requirements

Support SOP lifecycle management

and implementation of process changes relevant to offshore regional operations

Perform report reviews

ensuring data integrity

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

and support writing reports

and promptly with cross-functional stakeholders

Engage in continuous learning through self-study

Promote and adhere to safety

Ensure compliance with company procedures and all applicable regulatory requirements

How You'll Work.

Team & Collaboration

Coordinate closely with Project Management, laboratory teams, and stakeholders to ensure queries are addressed accurately and within defined timelines; Communicate clearly, accurately, and promptly with cross-functional stakeholders; Collaboration skills for working with internal stakeholders

Communication Scope

Communicate clearly, accurately, and promptly with cross-functional stakeholders

Process & Methodology

Pending list (PL) management, Query management, Study/Sponsor-specific support, SOP lifecycle management, Workflow monitoring

Full Job Description

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. Qual

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