Labcorp has announced an exciting opportunity for life sciences and pharmacy professionals through its Labcorp Hiring 2026 drive. The company is recruiting for the position of Associate Study Coordinator at its Bengaluru, India office.

This opportunity is particularly relevant for candidates with a Master’s degree in Pharmacy, Life Sciences, or a related scientific discipline who have experience in a pharmaceutical, scientific, or CRO environment. The role involves pharmacokinetic (PK) and toxicokinetic (TK) studies, study documentation, noncompartmental analysis, technical documentation, study scheduling, and archival activities.

Candidates with knowledge of PK/TK principles and Phoenix WinNonlin may have an advantage when applying for this Labcorp Associate Study Coordinator position.

Labcorp Associate Study Coordinator – Job Overview

About Labcorp

Labcorp is a global life sciences and laboratory services company supporting healthcare providers, patients, pharmaceutical companies, researchers, and health systems.

Through its diagnostics and drug development capabilities, Labcorp supports scientific research, clinical development, laboratory testing, and healthcare decision-making across global markets.

The Associate Study Coordinator job in Bengaluru provides an opportunity to work with scientific study data and documentation while developing expertise in pharmacokinetic and toxicokinetic study activities.

Job Responsibilities

As an Associate Study Coordinator at Labcorp, the selected candidate will be responsible for supporting PK and TK studies and associated study coordination activities.

Key responsibilities include:

• Conducting or supporting noncompartmental analysis (NCA) for pharmacokinetic and toxicokinetic studies.
• Reading and interpreting study protocols, amendments, study schedules, and sample analysis outlines.
• Understanding and following applicable regulatory requirements and Standard Operating Procedures (SOPs).
• Preparing, reviewing, and maintaining accurate study documentation.
• Supporting Study Coordinators with study finalization activities.
• Maintaining study schedules and supporting timely completion of study activities.
• Performing study archival activities according to established procedures.
• Preparing and editing technical documentation and ensuring error-free deliverables.
• Reviewing study-related tables and figures.
• Assisting with the preparation of tables and figures for PK/TK studies.
• Developing proficiency with data collection systems and reporting tools.
• Coordinating study phase schedules with Study Directors, Principal Investigators, and laboratory operations teams.
• Supporting other study coordination activities as required.

Qualifications

Candidates applying for the Labcorp Associate Study Coordinator vacancy should meet the following minimum qualification:

Master’s degree in Pharmacy, Life Sciences, or a related scientific discipline, or an equivalent combination of education and relevant experience.

The position requires approximately 1 year of relevant experience in a scientific, pharmaceutical, or CRO environment.

Preferred Skills

Candidates with the following skills and knowledge may be particularly suitable for the Associate Study Coordinator role:

• Knowledge of Pharmacokinetics (PK)
• Knowledge of Toxicokinetics (TK)
• Understanding of Noncompartmental Analysis (NCA)
• Experience with Phoenix WinNonlin
• Study protocol interpretation
• Scientific and technical documentation
• Study data review
• SOP and regulatory compliance
• Microsoft Excel
• Microsoft Word
• Microsoft Outlook
• Study scheduling and coordination
• Documentation and archival activities

Who Can Apply?

This Labcorp job may be suitable for candidates with postgraduate qualifications such as:

• M.Pharm
• M.Sc. Life Sciences
• M.Sc. Biotechnology
• M.Sc. Biochemistry
• M.Sc. Pharmacology
• M.Sc. Toxicology
• M.Sc. or equivalent qualification in another relevant scientific discipline

Candidates should ensure that their educational background and experience satisfy Labcorp’s stated requirements before applying.

Experience Required

Labcorp specifies 1 year of relevant experience in a scientific, pharmaceutical, or CRO environment.

Candidates with experience involving pharmacokinetics, toxicokinetics, study coordination, scientific documentation, preclinical research, bioanalysis, or related areas may find their background particularly relevant.

Work Schedule

The position is office-based at Labcorp’s Yashwantpur office in Bengaluru.

The scheduled shift is:

2:00 PM to 11:00 PM

Applicants should consider their ability to work this shift before submitting an application.

Benefits of This Opportunity

While specific compensation and employee benefits for this vacancy have not been disclosed in the job description, the role can provide valuable professional exposure to:

• Pharmacokinetic and toxicokinetic studies
• Noncompartmental analysis
• Phoenix WinNonlin
• Scientific study coordination
• Study documentation
• Regulatory and SOP-driven processes
• Technical documentation
• Study archival and finalization
• Cross-functional collaboration with scientific and laboratory teams

This experience can be valuable for professionals interested in building careers across pharmacokinetics, toxicokinetics, preclinical research, bioanalysis, CRO operations, and scientific study coordination.

Estimated Salary

Labcorp has not disclosed the salary for this position in the provided job posting.

For structured-data purposes only, an estimated market range of approximately ₹4,00,000–₹7,00,000 per year may be considered for a Bengaluru-based early-career study coordination role. This is an estimate and should not be represented as Labcorp’s advertised salary.

How to Apply

Application Link