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Coordinator Support I

Labcorp
0-2 years
₹2.5-6 LPA
Bangalore, India
10 June 10, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Apache Spark, Artificial Intelligence (AI), Big Data, Data Governance, Data Literacy, Data Management, Data Quality, Data Science, Data Strategies, Data Visualization, Machine Learning (ML), Master Da, Auditing, Audit Management, Audits Compliance, Communication, Continued Learning, Decision Making, Gmp Procedures, Inspection Readiness, Managing Ambiguity, Organizing, People Management and Leadershi, Bachelor’s Degree (BS) or Master’s Degree (MS) in: Life Sciences Pharmacy Biotechnology Biomedical Sciences Chemistry Regulatory Affairs Or related scientific disciplines, Budget Management, Clinical Trials, Negotiation Skills, Process Improvement, Project Planning, Vendor Management, Waterfall Model, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Causality Assessment, Change Control, Continual Improvement Process, Data Analytics and Digital, GDP Knowledge, gmp knowledge, HSE Knowledge, Manufacturing Process, Manufacturing Production, Operational Excellence, Process, Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems, Clinical Trials, Collaboration, Data Integrity, Decision Making Skills, Lifesciences, Clinical Research, Clinical Trials, Curious Mindset, Databases, Drug Development, Job Description, Lifesciences, Medical Communication, Medical Information, Medical Writing, Military Intelligence, Pat, Clinical SAS Programming, Clinical Trials, Cross-Functional Teams, Drug Development, Lifesciences, Negotiation Skills, People Management, Problem Solving Skills, Regulatory Compliance, Risk Management, Strategy Execution, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Clinical Trials, Functional Teams, Literature Review, Management Skills, Medical Information, Medical Records, Medical Strategy, Pharmacovigilance, Regulatory Compliance, Risk Management, Safety Scien, Coaching Skills, Data Science, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Pro, Collaboration, Communication Skills, gmp, GMP Guidelines, Operational Excellence, Problem Solving Skills, Quality Agreements, Quality Compliance, Quality Management, Quality Standards, Regulatory Requ, Communication Skills, Continual Improvement Process, Master Data, Material Requirements Planning (Mrp), Materials Management, People Management, Production Planning, Supplier Relationship Management (Srm), Supply-Chain Man, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, 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

Clinical Publishing Coordinator

Company Overview

Labcorp is a global leader in diagnostic testing and drug development solutions, supporting healthcare providers, researchers, and patients in improving healthcare outcomes.


Position Summary

The Clinical Publishing Coordinator is responsible for supporting clinical documentation activities by preparing, updating, and managing clinical trial-related documents. The role ensures accuracy, compliance, and timely delivery of all documentation required for clinical studies.


Key Responsibilities

1. Documentation Management

  • Create and modify:

    • Clinical Investigator Manuals

    • Requisitions

    • Other study-related documents as per SOW requirements

  • Ensure timely delivery of high-quality clinical documentation


2. Translation & Quality Support

  • Ensure assigned clinical documents are translated accurately and on time

  • Maintain consistency and quality in all documentation outputs


3. Compliance & SOP Adherence

  • Follow departmental:

    • Standard Operating Procedures (SOPs)

    • Work Instructions

    • Internal quality guidelines

  • Complete mandatory trainings within timelines


4. Coordination & Teamwork

  • Work effectively with cross-functional teams

  • Support smooth delivery of document packages

  • Escalate issues or delays when required


5. Operational Tasks

  • Complete daily assigned tasks with focus on quality and productivity

  • Perform additional duties assigned by management


Key Skills Required

  • Strong attention to detail

  • Good written and verbal communication

  • Ability to manage multiple priorities

  • Basic computer and documentation skills

  • Team collaboration

  • Time management

  • Ability to work in rotational shifts


Work Environment

  • Office-based role

  • Rotational shifts

  • Requires extended screen time

  • Multitasking and deadline-driven environment


Additional Requirements

  • Ability to handle interruptions while maintaining accuracy

  • Strong organizational skills

  • Consistent quality-focused work approach

  • Willingness to learn clinical documentation processes


Equal Opportunity Statement

Labcorp provides equal employment opportunities and promotes inclusion, diversity, and fairness in all hiring practices.