Clinical Research Job at Labcorp Bangalore
Looking to build a stable and rewarding Clinical Research Job career in a global CRO? This is a premium opportunity for life science graduates to join Labcorp as a Senior Clinical Project Administrator. With hands-on exposure to clinical trials, project coordination, and quality systems, this role is perfect for professionals aiming to grow in the clinical research domain.
About Labcorp
Labcorp is a global leader in diagnostic testing and drug development services. The company supports healthcare providers and researchers worldwide with innovative solutions. Known for offering top-tier Clinical Research Job opportunities, Labcorp is a preferred employer for professionals seeking roles like Senior Clinical Project Administrator and a great opportunity for life science graduates.
Job Details:
- Job Title: Senior Clinical Project Administrator
- Job ID: 2612578
- Location: Bangalore, Karnataka, India
- Company: Labcorp
- Category: Clinical
- Job Type: Full-Time
- Work Mode: Onsite
- Work Schedule: Rotating shift (5-day work week)
Role Overview
The Senior Clinical Project Administrator provides administrative and technical support to clinical project teams, ensuring efficient execution of project activities. The role focuses on documentation management, quality compliance, training coordination, and process improvement within a clinical research environment.
Key Responsibilities
- Follow departmental Standard Operating Procedures (SOPs) and Work Instructions
- Complete all required training within defined timelines
- Manage daily tasks while ensuring quality and productivity standards
- Maintain and manage project and technical documentation appropriately
- Provide administrative and technical support to internal teams
- Perform quality checks to ensure accuracy of completed work
- Ensure timely escalation and resolution of issues
- Track and report performance metrics as per management requirements
- Support implementation of revised processes and procedures
- Develop subject-matter understanding and provide solutions to process-related challenges
- Guide and mentor team members to achieve required competencies
- Maintain training records and ensure audit readiness at all times
- Track weekly and monthly training compliance for the team
- Participate in knowledge-sharing sessions across departments
- Assess workload and assign tasks/projects based on priority
- Perform peer quality checks and identify process gaps
- Suggest improvements to enhance quality and compliance
- Plan and deliver training sessions, including preparation of training materials
- Review and update SOPs/Work Instructions and coordinate with QA teams for documentation control
Candidate Profile
The ideal candidate is organized, detail-oriented, and capable of managing multiple tasks in a structured clinical environment. The individual should demonstrate strong communication skills, mentoring ability, and a commitment to quality and compliance.
Educational Qualification
- Bachelor’s Degree in Science
Preferred Qualifications
- Master’s Degree in Science
- Approximately 3 years of experience in the clinical research industry
Key Skills & Competencies
- Strong planning, prioritization, and organizational skills
- Effective communication and interpersonal abilities
- High attention to detail and quality orientation
- Ability to work collaboratively in a team environment
- Consistent delivery of high-quality work
- Proficiency in computer systems and departmental tools
Work Environment
Office-based clinical operations role with rotational shifts in a structured team setting. Exposure to global clinical research processes and quality systems.
