Global healthcare and drug development leader Labcorp has announced multiple hiring opportunities in Bengaluru, India. The company is currently recruiting for Document Coordinator I, Clinical Publishing Coordinator (Coordinator Support I), and Associate Programmer (Workfront Administrator II) positions.
These openings offer excellent career opportunities for candidates with backgrounds in life sciences, clinical research, quality documentation, and technology support. Professionals looking for clinical research jobs in Bangalore, document management jobs in pharma, and Workfront administrator jobs in India should consider applying.
About Labcorp
Labcorp is one of the world’s leading life sciences and healthcare companies, providing diagnostic testing, drug development solutions, and clinical research services globally. The organization supports pharmaceutical, biotechnology, and healthcare companies in advancing patient care and accelerating medical innovation.
1. Document Coordinator I
Location: Bengaluru, Karnataka, India
Work Model: Hybrid
Shift Timing: 9:00 AM โ 6:00 PM
Key Responsibilities
- Reformat and prepare controlled documents including SOPs and policies.
- Ensure document accuracy, consistency, and compliance.
- Manage documentation within Veeva QualityDocs and quality systems.
- Coordinate document reviews and approvals with SMEs and QA teams.
- Support implementation of approved documents.
- Maintain documentation records and compliance standards.
- Utilize Microsoft Office applications for document management.
- Handle multiple assignments while meeting deadlines.
Qualifications
- 1โ2 years of experience in document management or document control.
- Experience with document management systems.
- Knowledge of Veeva Vault QualityDocs preferred.
- Understanding of QMS processes.
- Familiarity with GLP/GCP regulations is advantageous.
- Strong communication and organizational skills.
2. Clinical Publishing Coordinator (Coordinator Support I)
Location: Bengaluru, Karnataka, India
Shift: Rotational
Key Responsibilities
- Prepare and update clinical investigator manuals and requisitions.
- Support creation of project-related clinical documentation.
- Coordinate language translations for study documents.
- Follow departmental SOPs and quality standards.
- Ensure timely delivery of clinical publishing activities.
- Escalate project issues when necessary.
- Maintain documentation quality and productivity targets.
Qualifications
- Bachelor’s Degree in Science.
- Master’s Degree preferred.
- 6 months or more experience in clinical research preferred.
- Strong attention to detail.
- Ability to manage multiple priorities.
- Excellent communication and teamwork skills.
3. Associate Programmer (Workfront Administrator II)
Location: Bengaluru, Karnataka, India
Work Schedule: MondayโFriday
Shift Timing: 2:00 PM โ 11:00 PM
Key Responsibilities
- Manage Adobe Workfront administration and support.
- Configure projects, templates, dashboards, and reports.
- Handle Level-1 and Level-2 support tickets.
- Create and maintain SOPs and governance standards.
- Support Workfront Fusion automation initiatives.
- Develop dashboards and reporting solutions.
- Manage user permissions and workflow configurations.
- Train end-users and provide technical support.
Overall Qualification (All 3 Roles)
Bachelor’s Degree in Science, Life Sciences, Pharmacy, Biotechnology, Biotechnology-related disciplines, Technology/Engineering, or relevant equivalent qualification.
Experience Required (Role-wise)
- Document Coordinator I โ 1โ2 years experience in document management, document control, quality documentation, or related field.
- Clinical Publishing Coordinator (Coordinator Support I) โ 0โ6 months to 1 year experience (Freshers with B.Sc. eligible; clinical research experience preferred).
- Associate Programmer (Workfront Administrator II) โ 3+ years experience in Adobe Workfront development and 1.5+ years experience in Workfront support/administration.
Why Join Labcorp?
Labcorp offers employees the opportunity to work with a globally recognized healthcare and drug development organization. Benefits include:
- Global career growth opportunities
- Exposure to pharmaceutical and clinical research projects
- Hybrid work opportunities for selected roles
- Learning and development programs
- Inclusive and diverse workplace culture
- Competitive compensation and benefits
How to Apply
Application Link For Document Coordinator I
Application Link For Clinical Publishing Coordinator (Coordinator Support I)
Application Link For Associate Programmer (Workfront Administrator II)
