Are you looking for an entry-level position in the clinical research or laboratory industry? Labcorp is hiring for two exciting roles in Bangalore, India: Report Writer Coordinator I and Informed Consent Codification Associate. These full-time positions offer a great opportunity to kickstart your career in a fast-paced, globally recognized organization. Read on to learn more about these roles, their responsibilities, and how to apply before the deadline on March 4, 2025.
1. Report Writer Coordinator I: An Entry-Level Role in Clinical Documentation
Job Overview
The Report Writer Coordinator I is an entry-level position within the LMVRS (Laboratory Manual and Report Writing Services) group at Labcorp. This role focuses on learning and applying Labcorp’s writing standards to draft, edit, and ensure consistency in clinical trial reports.
Key Responsibilities
- Learn and utilize software tools to efficiently complete job duties.
- Draft and edit lower-complexity clinical trial documents using pre-defined templates or client-supplied information.
- Create data tables using corresponding databases.
- Perform quality control (QC) and review documents to ensure compliance with company conventions, style, and terminology.
- Manage workload using tracking tools and ensure timely completion of tasks.
- Maintain and develop training manuals.
- Provide backup assistance to colleagues as needed.
Skills and Qualifications
- Strong attention to detail and organizational skills.
- Ability to manage time effectively and meet deadlines.
- Basic understanding of clinical trial protocols and SOPs (Standard Operating Procedures).
- Proficiency in Microsoft Office tools (Word, Excel).
- Excellent written and verbal communication skills.
2. Informed Consent Codification Associate: Ensuring Compliance in Clinical Trials
Job Overview
The Informed Consent Codification Associate role focuses on managing and codifying informed consent forms for clinical trials. This position ensures compliance with global regulations and maintains data integrity across multiple client instances.
Key Responsibilities
- Perform informed consent codification accurately and efficiently.
- Troubleshoot and resolve errors in codification processes.
- Maintain knowledge of SOPs and validation work procedures.
- Support process improvement initiatives, including Six Sigma projects.
- Mentor and train other employees on informed consent codification.
- Assist with special projects and other duties as assigned.
Skills and Qualifications
- 0-1 year of experience in clinical trials, laboratory, or specimen management.
- Knowledge of informed consent forms and global regulations.
- Strong analytical and problem-solving skills.
- Proficiency in Microsoft Office, especially Excel and Word.
- Excellent communication and interpersonal skills.
- Familiarity with 21 CFR Part 11 regulations is a plus.
Why Join Labcorp?
Labcorp is a global leader in life sciences and healthcare, offering a dynamic work environment with opportunities for growth and development. By joining Labcorp, you will:
- Gain hands-on experience in clinical research and documentation.
- Work with a team of experienced professionals.
- Contribute to impactful projects that improve patient outcomes.
- Enjoy a supportive workplace culture that values innovation and collaboration.
How to Apply
Don’t miss this opportunity to join Labcorp in Bangalore, India! The application deadline is March 4, 2025.
Application Link For Informed Consent Codification Associate
Application Link For Report Writer Coordinator I
