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Labcorp Hiring For Controlled Docs Coordinator | Clinical Trials

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Labcorp

B.Sc / M.Sc in Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharmacy (B.Pharm/M.Pharm), or other relevant Science disciplines.

Bengaluru, India

6 months

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Labcorp has announced a new Controlled Docs Coordinator job in Bengaluru for candidates with a Bachelor’s degree in Science and current or prior Labcorp internship experience. This full-time opportunity is suitable for candidates interested in clinical research documentation, controlled document management, regulatory compliance, and quality assurance.

As a Controlled Docs Coordinator at Labcorp, the selected candidate will support the administration and maintenance of controlled documents while ensuring documents are available to authorized end users and handled according to applicable Standard Operating Procedures (SOPs), Work Instructions, and regulatory requirements.

The position follows a Monday–Friday general shift. Candidates looking to build their careers in clinical research documentation and quality operations can review the eligibility requirements below and apply before August 21, 2026.

Labcorp Controlled Docs Coordinator Job Overview

Job DetailsInformation
CompanyLabcorp
PositionControlled Docs Coordinator
LocationBengaluru, India
Job TypeFull-Time
Work ScheduleMonday–Friday, General Shift
QualificationBachelor’s degree in Science
Preferred QualificationMaster’s degree in Science
ExperienceCurrent/prior Labcorp internship; 6 months relevant clinical research experience preferred
Job ID2627499
Application DeadlineAugust 21, 2026

About Labcorp

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

The organization combines laboratory science, data, technology, diagnostics, and clinical research capabilities to support healthcare decision-making, accelerate innovation, and improve patient outcomes globally.

The Labcorp Controlled Docs Coordinator position provides an opportunity to work in an environment focused on document control, quality, compliance, and clinical research operations.

Key Responsibilities

Candidates selected for the Controlled Docs Coordinator job at Labcorp will be responsible for:

  • Following applicable departmental Standard Operating Procedures (SOPs) and Work Instructions.
  • Completing mandatory training within established timelines.
  • Performing assigned day-to-day activities while maintaining productivity and quality standards.
  • Administering controlled documents and ensuring their availability to end users.
  • Maintaining an accurate inventory of controlled documents.
  • Conducting quality checks on completed work.
  • Identifying and escalating issues that could affect the timely release of controlled documents.
  • Supporting appropriate resolution management for document-release issues.
  • Ensuring applicable Regulatory Compliance and Quality Assurance (RC&QA) responsibilities are followed.
  • Completing other responsibilities assigned by management.

Eligibility & Qualifications

Minimum Qualifications

Applicants should have:

  • Bachelor’s degree in Science
  • Current or prior Labcorp intern experience

The prior Labcorp internship requirement is specifically included under the minimum qualifications in the job description and should be considered by candidates before applying.

Preferred Qualifications

Labcorp prefers candidates with:

  • Master’s degree in Science
  • Approximately 6 months of relevant experience in the clinical research industry

Candidates should carefully review the official application page for the final eligibility requirements before submitting their application.

Skills Required

Candidates interested in the Labcorp Controlled Docs Coordinator vacancy should demonstrate:

  • Strong organizational skills
  • Effective communication
  • Excellent attention to detail
  • Ability to collaborate with team members
  • Consistent delivery of high-quality work
  • Basic computer proficiency
  • Ability to use departmental systems and tools
  • Understanding of controlled documentation practices
  • Quality and compliance-oriented working approach

Knowledge of SOPs, document control, Quality Assurance, regulatory compliance, and clinical research documentation may be particularly relevant to the responsibilities of this role.

Why Consider This Opportunity?

The Controlled Docs Coordinator role can provide exposure to several important areas within regulated clinical research operations, including:

  • Controlled document management
  • SOP and Work Instruction compliance
  • Quality checks
  • Regulatory compliance
  • Quality Assurance processes
  • Clinical research documentation
  • Document inventory management
  • Issue escalation and resolution

This experience can be relevant for candidates interested in developing careers involving clinical documentation, Quality Assurance, document control, regulatory operations, and clinical research support.

Salary for Labcorp Controlled Docs Coordinator

Labcorp has not disclosed a salary range in the provided job description.

For structured-data purposes, an estimated market range of approximately ₹3.0 lakh to ₹5.0 lakh per year may be used as a clearly identified estimate rather than represented as an employer-disclosed salary.

Actual compensation may differ depending on the candidate’s qualifications, relevant experience, internal compensation policies, and other factors.

How to Apply

Application Link

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