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Labcorp Hiring Associate Study Coordinator | Clinical Trials

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Labcorp

Master's degree in Pharmacy, Master's in Life Sciences, equivalent scientific qualification

Bengaluru

1 year in Clinical Research

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Labcorp, one of the world’s leading global life sciences and laboratory services companies, has announced recruitment for the position of Associate Study Coordinator at its Bengaluru (Yeshwanthpur) office. This opportunity is ideal for candidates with an M.Pharm, Life Sciences, or related scientific degree and around 1 year of experience in pharmaceutical research, pharmacokinetics (PK), toxicokinetics (TK), or a CRO environment.

If you’re looking for a Labcorp Associate Study Coordinator job in Bengaluru, this role offers exposure to pharmacokinetic studies, study coordination, technical documentation, and collaboration with global clinical research teams.


Job Overview

DetailsInformation
CompanyLabcorp
PositionAssociate Study Coordinator
Job TypeFull-Time
LocationBengaluru (Yeshwanthpur), Karnataka
Shift2:00 PM โ€“ 11:00 PM
ExperienceMinimum 1 Year
QualificationM.Pharm, Life Sciences, or related scientific degree
IndustryClinical Research / CRO / Pharmacokinetics
Application DeadlineJuly 27, 2026

About Labcorp

Labcorp is a globally recognized leader in laboratory services, diagnostics, clinical research, and drug development solutions. The company partners with pharmaceutical, biotechnology, and healthcare organizations worldwide to accelerate innovation and improve patient outcomes through advanced science, technology, and data-driven healthcare solutions.

Working at Labcorp provides opportunities to contribute to global clinical research while developing expertise in pharmacokinetics, toxicology, laboratory sciences, and study coordination.


Key Responsibilities

The selected Associate Study Coordinator will be responsible for:

  • Supporting pharmacokinetic (PK) and toxicokinetic (TK) studies
  • Conducting or assisting with Non-Compartmental Analysis (NCA)
  • Reading and interpreting study protocols and amendments
  • Preparing and reviewing study documentation
  • Maintaining study schedules and documentation
  • Supporting study archival activities
  • Reviewing technical reports, tables, and figures
  • Preparing high-quality scientific documentation
  • Coordinating with Study Directors and laboratory teams
  • Assisting in study finalization and reporting
  • Learning Labcorp’s data collection and reporting systems
  • Ensuring compliance with SOPs and regulatory requirements

Required Qualifications

Applicants should possess:

  • Master’s degree in Pharmacy
  • Master’s in Life Sciences
  • Or equivalent scientific qualification

Experience required:

  • Minimum 1 year in Pharmaceutical Industry
  • Clinical Research Organization (CRO)
  • Pharmacokinetics
  • Toxicokinetics
  • Scientific Research

Preferred skills include:

  • Pharmacokinetic (PK) knowledge
  • Toxicokinetic (TK) understanding
  • Phoenix WinNonlin software
  • Microsoft Excel
  • Microsoft Word
  • Microsoft Outlook
  • Technical documentation
  • Strong communication skills
  • Time management
  • Team collaboration

Preferred Technical Skills

Candidates with exposure to the following areas will have an advantage:

  • Non-Compartmental Analysis (NCA)
  • PK Data Analysis
  • TK Studies
  • Phoenix WinNonlin
  • Study Scheduling
  • Scientific Documentation
  • Regulatory Compliance
  • SOP Management
  • Clinical Research Documentation
  • Laboratory Coordination

Why Join Labcorp?

Working with Labcorp offers several career advantages:

  • Global CRO and laboratory services leader
  • International research exposure
  • Structured career growth
  • Pharmacokinetics specialization
  • Scientific documentation experience
  • Collaborative work environment
  • Exposure to regulated research processes
  • Opportunity to work on global pharmaceutical projects
  • Stable multinational organization
  • Competitive compensation and employee benefits

Salary (Estimated)

Based on similar Associate Study Coordinator roles in Bengaluru, the expected annual salary is:

โ‚น5.5 Lakhs โ€“ โ‚น8.5 Lakhs per annum (CTC)

Actual salary may vary depending on experience, qualifications, and internal compensation policies.


Work Schedule

  • Office-Based Role
  • Second Shift
  • 2:00 PM โ€“ 11:00 PM

Who Should Apply?

This position is suitable for:

  • M.Pharm graduates
  • Life Sciences postgraduates
  • Pharmacology professionals
  • Clinical Research professionals
  • CRO professionals
  • Pharmacokinetic Analysts
  • Toxicokinetic Researchers
  • Study Coordinators
  • Drug Development professionals
  • Candidates with 1 year of pharmaceutical research experience

How to Apply

Application Link

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