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Associate Study Coordinator

Labcorp
0-2 years
Not Disclosed
Bengaluru, India
8 May 22, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Company

Labcorp

Job Title

Associate Study Coordinator

Location

Bengaluru

Employment Type

  • Full-time

  • Remote-based

  • 2nd Shift

  • 40 hours per week

Application Deadline

  • Apply by: May 24, 2026


Role Summary

Labcorp is hiring an Associate Study Coordinator to support pharmacokinetic (PK) and toxicokinetic (TK) studies. The role involves study coordination, documentation review, data analysis support, scheduling, and archival activities within a regulated research environment.


Key Responsibilities

Study & Data Support

  • Conduct or assist with noncompartmental analysis (NCA) for PK/TK studies

  • Support preparation of tables and figures

  • Learn and use data collection and reporting systems

  • Review study-related tables and figures prepared by team members

Documentation & Compliance

  • Read and interpret:

    • Study protocols

    • Sample analysis outlines

    • Study schedules

    • Amendments

    • SOPs and regulatory requirements

  • Prepare, edit, and review documentation for accuracy and completeness

  • Ensure timely submission of deliverables

Study Coordination

  • Coordinate study phase scheduling with:

    • Study Directors (SD)

    • Principal Investigators (PI)

    • Laboratory operations teams

  • Assist with study finalization activities

  • Support archival scheduling and maintenance

Archival Activities

  • Perform study archival tasks

  • Maintain study records and schedules

Additional Duties

  • Complete other assigned tasks and operational responsibilities


Required Qualifications

Education

  • Master’s degree in:

    • Pharmacy

    • Life Sciences

    • Related field
      (or equivalent experience)

Experience

  • 0–2 years of relevant experience

Technical Skills

  • Basic Microsoft Office skills:

    • Word

    • Excel

    • Outlook

  • Knowledge of Phoenix WinNonlin preferred

Soft Skills

  • Strong written and verbal communication

  • Ability to multitask in a fast-paced environment

  • Good organizational and deadline-management skills


Preferred Skills

  • Exposure to pharmacokinetic/toxicokinetic studies

  • Familiarity with clinical or bioanalytical research workflows

  • Experience with scientific documentation and reporting tools