Labcorp Hiring Coordinator Support I – B.Pharmacy Freshers
- Labcorp Hiring Coordinator Support I – B.Pharmacy Freshers | Bengaluru Clinical Documentation Jobs
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Clinical Documentation & Publishing Support
- Collaboration & Process Execution
- Quality & Compliance
- Eligibility / Qualifications
- Educational Qualification
- Experience
- Skills Required
- Preferred Qualifications
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- 1. Who can apply for this role?
- 2. Is prior experience required?
- 3. What are the main responsibilities?
- 4. What is the career growth?
- 5. Is this a good entry-level pharma job?
- Summary Table
Labcorp Hiring Coordinator Support I – B.Pharmacy Freshers | Bengaluru Clinical Documentation Jobs
Labcorp is hiring Coordinator Support I professionals for its Clinical division in Bengaluru, India (Brigade Twin Towers, Yeshwanthpur). This is a full-time, on-site opportunity ideal for B.Pharmacy freshers and candidates with around 6 months of clinical research experience. The role focuses on clinical documentation, investigator materials, and regulatory-compliant publishing support, making it a strong entry-level opportunity in clinical research and pharmaceutical documentation careers.
Company Overview
Labcorp is a globally recognized life sciences and diagnostics company that partners with pharmaceutical, biotechnology, and healthcare organizations to support clinical trials, laboratory testing, and drug development. With a strong global footprint and expertise in clinical research services, Labcorp plays a critical role in accelerating the development of new therapies.
The organization is known for maintaining high standards in regulatory compliance, clinical documentation, and data integrity. Working at Labcorp provides exposure to global clinical trials, regulatory publishing processes, and advanced clinical operations systems, making it a strong platform for career growth in healthcare and life sciences.
Job Role & Responsibilities
As a Coordinator Support I, you will be responsible for supporting clinical publishing and documentation activities while ensuring compliance with regulatory guidelines and project timelines.
Core Responsibilities
- Follow Standard Operating Procedures (SOPs), work instructions, and departmental guidelines
- Complete assigned tasks with high quality and productivity standards
- Create and update clinical investigator manuals, requisitions, and study-related documentation
- Support clinical documentation preparation as per project requirements and timelines
Clinical Documentation & Publishing Support
- Assist in preparation and modification of clinical trial documents
- Ensure timely completion of language translations for study-related materials
- Maintain accuracy, consistency, and compliance in all documentation outputs
Collaboration & Process Execution
- Work effectively with team members to ensure timely delivery of documentation
- Escalate issues proactively to maintain workflow efficiency
- Participate in required training programs and stay updated with clinical publishing practices
Quality & Compliance
- Ensure all deliverables meet regulatory and internal quality standards
- Handle multiple tasks and priorities in a fast-paced clinical research environment
- Support audit readiness and documentation accuracy
Eligibility / Qualifications
Educational Qualification
Candidates must have a degree in Pharmacy or related life sciences discipline.
Required courses include:
B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Biotechnology, Microbiology, Biochemistry, Life Sciences), Biomedical Sciences, Clinical Research
Experience
- Freshers can apply
- 6 months of clinical research or documentation experience preferred
Skills Required
- Basic understanding of clinical research and documentation workflows
- Strong attention to detail and organizational skills
- Good written and verbal communication skills
- Ability to manage multiple tasks and meet deadlines
- Proficiency in MS Office tools
Preferred Qualifications
- Master’s degree in Biotechnology or related discipline
- Exposure to clinical publishing or regulatory documentation
Location & Salary
- Job Location: Bengaluru, Karnataka, India
- Employment Type: Full-time (On-site)
- Work Schedule: Rotational shifts
- Salary: Competitive salary aligned with entry-level clinical research and documentation roles
Application Process
Interested candidates can apply through the official Labcorp careers portal:
Apply Here: https://careers.labcorp.com/global/en/job/268880 fileciteturn1file0
Frequently Asked Questions (FAQs)
1. Who can apply for this role?
Candidates with B.Pharmacy or Life Sciences backgrounds can apply. Freshers are eligible.
2. Is prior experience required?
No. Freshers can apply, though 6 months of clinical research experience is preferred.
3. What are the main responsibilities?
The role involves clinical documentation preparation, publishing support, and regulatory compliance tasks.
4. What is the career growth?
You can grow into Clinical Data Management, Regulatory Publishing, or Clinical Operations roles.
5. Is this a good entry-level pharma job?
Yes. It is a strong entry point into clinical research and regulatory documentation careers.
Summary Table
| Category | Details |
|---|---|
| Company | Labcorp |
| Vacancies | Coordinator Support I |
| Required Education | B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Biotechnology, Microbiology, Biochemistry, Life Sciences), Biomedical Sciences, Clinical Research |
| Experience | Freshers / 6 Months Experience |
To apply for this job please visit careers.labcorp.com.
