Labcorp Hiring Clinical Report Writer Coordinator – Entry-Level Opportunity in Bangalore

Labcorp Clinical Report Writer Coordinator Job Vacancies

Labcorp, a global leader in life sciences and healthcare solutions, is hiring a Clinical Report Writer Coordinator in Bangalore, India. This entry-level position offers an exciting opportunity to develop expertise in clinical trial documentation, working within a dynamic team environment. If you have a passion for clinical writing and are ready to kick-start your career, this role is for you!

Labcorp Hiring Clinical Report Writer Coordinator

Labcorp is actively seeking a dedicated and detail-oriented individual to join their LMVRS (Labcorp Medical Writing and Reporting Services) team. As a Clinical Report Writer Coordinator, you will contribute to producing high-quality clinical trial documentation that supports research and innovation in healthcare.

Key Job Details

• Job Title: Clinical Report Writer Coordinator I
• Category: Clinical
• Location: Bangalore, India
• Job ID: 2444315
• Job Type: Full-Time

Job Responsibilities

As a Clinical Report Writer Coordinator, you will:

The Report Writer Coordinator is an entry level position in the LMVRS group, learning the Labcorp writing standard and learning to draft and edit reports to promote product consistency.

• Learns to use software tools to efficiently and accurately complete job duties.
• Learns and understands any new/changed conventions or standard language.
• Creates report folders and requests all needed information, documentation and any other relevant information from the respective departments.
• Creates part of the initial draft of lower complexity clinical trials internal or client facing documents using pre-defined templates or client-supplied information with guidance from more senior colleagues and using study protocol information, SOPs and/or lab data.
• Creates data tables, as needed, using the corresponding database(s).
• Performs review and quality control (QC) as applicable.
• Edits internal or client facing documents, as needed, after review, ensuring that company convention, style, format and terminology have been used.
• Independently utilizes workload management tool to track and document data and report completion activities.
• Ensures compliance to applicable departmental Standard Operating Procedures and Work Instructions.
• Maintains/develops training manuals.
• Effectively manages own time and deadlines.
• Effectively manages task status tracking and time recording.
• May provide backup assistance to colleagues, as appropriate.
• Performs other duties as assigned.

Eligibility Criteria

To apply for this role, candidates must possess:

• Strong writing and communication skills.
• Proficiency in using software tools for data management and document creation.
• Excellent time management abilities.

This position is ideal for individuals eager to grow in the field of clinical writing within a supportive and innovative organization.

How to Apply

To apply for the Clinical Report Writer Coordinator role, visit the official Labcorp careers page at the link below:

Apply Here

Equal Opportunity Employer Statement

Labcorp is proud to be an Equal Opportunity Employer. Employment decisions are based on qualifications and business needs, without discrimination based on race, gender, religion, or other protected characteristics.

Tagged as: Good Clinical Practice (GCP)