Labcorp Hiring Clinical Document Coordinator – Bangalore

Labcorp; Bengaluru; On-site; INR 400,000 - 600,000; Full time

Job summary

Labcorp is seeking a detail-oriented Clinical Document Coordinator for Bangalore. The role focuses on managing controlled documents, formatting, and quality control in support of Safety Assessment Operations.

Qualifications include an associate degree in the laboratory or medical nursing and at least one year of quality control/assurance or pre-clinical experience, with proficiency in MS Office and familiarity with GLP/GCP regulatory requirements.

Qualifications

• Associate degree in the laboratory, medical nursing, or equivalent is required.
• Minimum 1 year of experience in quality control/assurance or pre-clinical work.
• Knowledge of GLP/GCP and regulatory requirements is advantageous.
• Proficiency with MS Office applications.

Responsibilities

• Document Preparation and Formatting: Reformat and prepare controlled documents to meet templates.
• Coordination and Quality Control: Review by SMEs and ensure timely acceptance into use.
• System Management: Be conversant with Labcorp Quality Systems including Veeva Quality Docs.

Skills

Attention to detail

Organizational skills

Time management

Communication skills

Analytical thinking

Education

Associate degree in laboratory/medical nursing

Tools

MS Office

Job description

Labcorp Hiring Clinical Document Coordinator – Bangalore

Labcorp is seeking a dedicated and detail-oriented Clinical Document Coordinator to join our team in Bangalore. This full-time role requires candidates with a background in quality control, quality assurance, or pre-clinical experience. If you have an Associate degree in Laboratory or Medical Nursing and are passionate about clinical documentation, we encourage you to apply.

Job Overview

As a Clinical Document Coordinator at Labcorp, you will be crucial in supporting Safety Assessment Operations. Your responsibilities will include managing administrative tasks, documentation, and quality control related to controlled document formatting and processing. This position ensures that all documents meet the required standards and templates, adhering to regulatory requirements and company guidelines.

Key Responsibilities

• Document Preparation and Formatting:
  • Reformat and prepare controlled documents, such as Policies and Standard Operating Procedures (SOPs), to ensure they meet current requirements and established templates.
  • Review document formats to ensure quality standards are met.
• Coordination and Quality Control:
  • Coordinate the review of controlled documents by Subject Matter Experts (SMEs).
  • Work with SMEs and Quality Assurance to successfully drive the acceptance of controlled documents into operational use.
  • Ensure the quality and timeliness of all personal work performed meets required standards.
• System Management:
  • Be fully conversant with Labcorp Quality Systems, including Veeva Quality Docs.
  • Perform other related duties as assigned.

Qualifications

• Education:
  • An associate degree in the laboratory, medical nursing, or equivalent is required.
  • Experience may be substituted for educational requirements.
• Experience:
  • Minimum 1 year of experience in quality control/assurance or pre-clinical experience.
  • Competency with MS Office applications.
  • Knowledge of GLP/GCP and regulatory requirements is advantageous.
• Skills:
  • Excellent attention to detail.
  • Good organizational and time management skills.
  • Strong communication skills.
  • Good verbal, numerical, and visual skills.
  • Ability to foster a high professional standard and encourage good staff relationships.
  • Conscientious, disciplined, flexible, and adaptable.

Equal Opportunity Employer

Labcorp is proud to be an Equal Opportunity Employer. We strive for diversity and inclusion in the workforce and do not tolerate harassment or discrimination. Employment decisions are based on our business’s needs and the individual’s qualifications. We encourage all qualified candidates to apply.

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