Associate 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 an Associate Study Coordinator to join our team in Bangalore, Yashwantpur office.

Work Schedule

• Office-based
• 2nd Shift (2PM - 11PM)

Job Responsibilities

• Conduct or support noncompartmental analysis (NCA) for pharmacokinetic (PK) and toxicokinetic (TK) studies.
• Read and interpret study protocols, sample analysis outlines, amendments, study schedules, applicable regulatory requirements, and standard operating procedures (SOPs).
• Prepare, review, and maintain study documentation, ensuring accuracy, completeness, and timely delivery.
• Collaborate with Study Coordinators to support study finalization and archival activities, including maintaining study schedules.
• Perform study archival activities in compliance with established procedures.
• Prepare and edit technical documentation to ensure high-quality, error-free deliverables.
• Review tables and figures generated by team members and assist in preparing study-related tables and figures.
• Develop proficiency in data collection systems and reporting tools used for pharmacokinetic and toxicokinetic studies.
• Coordinate study phase scheduling with Study Directors, Principal Investigators, and laboratory operations teams.
• Support additional study coordination activities and perform other duties as assigned.

• Master's degree in Pharmacy, Life Sciences, or a related scientific field (or equivalent combination of education and experience).
• 1 year of relevant experience in a scientific, pharmaceutical, or CRO environment.

• Knowledge of pharmacokinetic (PK) and toxicokinetic (TK) principles is preferred.
• Experience with Phoenix WinNonlin
• Proficiency in Microsoft Office applications, including Word, Excel, and Outlook.

• Strong organizational skills with the ability to manage multiple priorities and meet deadlines.
• Excellent written and verbal communication skills.
• Ability to work effectively in a collaborative, team-oriented environment.