The Report Writer Coordinator I position at Labcorp in Bangalore, India, is an entry-level role within the Laboratory Medicine Validation and Reporting Services (LMVRS) group. Here’s a detailed explanation of the role and its requirements:

Role Overview:

The position involves drafting, editing, and coordinating reports for clinical trials while adhering to Labcorp’s writing standards. It is primarily a learning and training opportunity for candidates to develop skills in clinical documentation, quality control, and compliance.

Key Responsibilities:

1. Learning and Training:
   • Develop expertise in Labcorp’s writing conventions and software tools.
   • Understand and adapt to changes in conventions, standard language, and style.
2. Report Drafting and Documentation:
   • Create report folders and gather necessary information from various departments.
   • Draft initial reports for lower-complexity clinical trials using predefined templates and client-supplied data.
   • Create data tables using the corresponding database.
3. Quality Control and Editing:
   • Perform review and QC of reports to ensure compliance with company conventions.
   • Edit client-facing or internal documents, ensuring consistency in style and terminology.
4. Task Management:
   • Use workload management tools to document data and track task progress.
   • Ensure effective time management and adherence to deadlines.
5. Compliance and Training:
   • Follow departmental SOPs and work instructions.
   • Contribute to training material development and maintenance.
6. Support:
   • Provide backup assistance to team members when required.
   • Perform additional duties as assigned.

Key Skills and Competencies:

• Attention to Detail: Ensure accuracy and quality in reports.
• Writing and Editing Skills: Proficiency in drafting, editing, and formatting documents.
• Software Proficiency: Ability to learn and use report-writing tools and databases efficiently.
• Time Management: Manage deadlines effectively and prioritize tasks.
• Collaboration: Work with multiple departments and provide support as needed.
• Compliance Knowledge: Adherence to SOPs and regulatory guidelines.

Opportunities:

This role provides:

• Exposure to the clinical trials domain.
• Training in report-writing standards and tools.
• A pathway to advance within the organization by gaining relevant skills and experience.

Application Link