Clinical Research Job at Labcorp Careers | Associate Study Coordinator role | M Pharm freshers | Apply Now
Looking for a Clinical Research Job in the pharmaceutical and research industry? Labcorp is hiring for the Associate Study Coordinator role in Bangalore under Labcorp Careers. This opportunity is ideal for Pharmacy candidates seeking hands-on experience in pharmacokinetics, toxicokinetics, study coordination, and clinical research operations in a global healthcare organization.
- Job Title: Associate Study Coordinator
- Category: Research and Development
- Location: Bangalore, India
- Job ID: 2616691
About the Company
Labcorp is a leading global life sciences and healthcare company providing laboratory services, diagnostic solutions, and drug development support. Through innovation and scientific expertise, the company supports healthcare providers and pharmaceutical organizations worldwide. Labcorp Careers offers excellent growth opportunities for professionals interested in research, diagnostics, and clinical development.
Job Description
Labcorp is seeking an Associate Study Coordinator to join its Bangalore office. This Clinical Research Job involves supporting pharmacokinetic (PK) and toxicokinetic (TK) studies, reviewing documentation, assisting in study archival activities, and coordinating with research and lab operations teams. Candidates will gain practical exposure to clinical research workflows and reporting systems through Labcorp Careers.
Key Responsibilities
- Conduct or support noncompartmental analysis (NCA) for pharmacokinetic (PK) and toxicokinetic (TK) studies.
- Learn to read and interpret study protocols, sample analysis outlines, amendments, study schedules, and applicable regulatory requirements and SOPs.
- Assist in preparing and reviewing documentation, ensuring accuracy, completeness, and timeliness.
- Collaborate with other Study Coordinators to manage study finalization and archival activities, including maintaining associated schedules.
- Perform tasks related to study archival.
- Prepare and edit documentation to ensure error-free deliverables.
- Learn to review tables and figures prepared by team members.
- Assist in the preparation of tables and figures, developing proficiency with data collection systems and reporting tools.
- Support study phase scheduling in coordination with Study Directors/Principal Investigators (SD/PI) and lab operations.
- Carry out additional tasks and responsibilities as assigned.
Qualifications
- Master’s degree in Pharmacy, Life Sciences, or a related field (or equivalent experience).
- 0–2 years of relevant experience.
- Ability to manage multiple tasks and meet deadlines in a fast-paced environment.
- Basic proficiency in Microsoft Office (Word, Excel, Outlook).
- Experience with Phoenix WinNonlin is preferred.
- Strong written and verbal communication skills.
