Associate study coordinator (Labcorp)

Roles and Responsibilities

• Job 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.

• Minimum Qualifications

• Master’s degree in Pharmacy, Life Sciences, or a related field (or equivalent experience), with 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.