Technical Study Coordinator

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.

Labcorp is seeking a Technical Study Coordinator to join our team at Bangalore, Yeshwantpur office.

2nd Shift - 2 PM - 11PM

• 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.

• 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.

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 

We encourage all to apply

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