Clinical Research Job at Labcorp
Ready to take the next step in your research career? This Clinical Research Job at Labcorp Careers offers an exciting opportunity for life science graduates to join one of the world’s leading healthcare and laboratory service organizations. As a Technical Study Coordinator in Bengaluru, you will support nonclinical research studies, coordinate study documentation, and contribute to innovative scientific projects. If you’re searching for a rewarding Life Science Job with global exposure and career growth, this opportunity is worth exploring.
About Labcorp
Labcorp is a global leader in laboratory services, diagnostics, and life science innovation. The company partners with healthcare providers, pharmaceutical organizations, researchers, and biotechnology companies to improve patient outcomes through advanced diagnostics, scientific expertise, and cutting-edge technologies. With operations across multiple countries, Labcorp Careers provides professionals with opportunities to contribute to meaningful healthcare innovations while building successful careers in research, diagnostics, and laboratory sciences.
Job Details:
- Job Title: Technical Study Coordinator
- Category: Research and Development
- Location: Bangalore, India
- Job ID: 2621786
- Job Type: Full-Time
- Remote: No
Job Responsibilities
- Support the execution of nonclinical studies by coordinating study support activities.
- Assist with the compilation of Historical Control Data to support the DART business.
- Support Study Director management in monitoring departmental and Study Director workloads.
- Provide administrative backup support for Study Directors on day-to-day study-specific activities and tasks.
- Maintain complete, organized, and current study files, including study schedules, protocols, amendments, and study correspondence.
- Draft study protocols and protocol amendments for Study Director review and approval, as applicable.
- Perform basic data quality checks to ensure accuracy and completeness of study data.
- Ensure study documentation is maintained in compliance with applicable procedures and study requirements.
- Provide general administrative and non-study-specific support to key clients and other functions within DART Scientific Support.
Minimum Qualifications
- Bachelor’s degree in a related scientific field, or an equivalent combination of education and experience. Relevant experience may be substituted for education.
- Minimum of 1 year of experience supporting preclinical and/or clinical research studies.
- Prior experience with Historical Control Data compilation is preferred but not required.
- Strong organizational skills with exceptional attention to detail and accuracy.
- Effective written and verbal communication skills with strong interpersonal abilities.
- Proficiency with Microsoft Office applications and the ability to learn electronic data capture (EDC) systems and other research software.
- Ability to manage multiple priorities while working independently and collaboratively in a fast-paced environment.
