
location_on2925, H Street, Marshall School, East Sacramento, Sacramento, Sacramento County, California, 95816, United States
The Clinical Laboratory Study Manager serves as a critical bridge between scientific strategy and operational execution. Working closely with the Precision Medicine Strategy Lead, clinical study teams, and specialized groups such as Data Management, Samples, Kits, Data, Logistics (SKDL), and Clinical Laboratory Project Management (CLPM), this role ensures the delivery of high-quality samples and data. The primary mission is to support biomarker and non-biomarker evaluations, enabling the translation of scientific discoveries into effective medicines.
In this position, you will oversee the entire lifecycle of clinical sample management, from collection and chain of custody to usage per informed consent forms, tracking, and eventual destruction. You will act as a key liaison between internal stakeholders and external vendors, ensuring that sample collection aligns strictly with study protocols. Your expertise will be vital in resolving sample-related queries and supporting Clinical Trial Management (CTM) and CRO partners to maintain data integrity throughout the trial.
Your work involves active participation in cross-functional study teams, collaborating on the development of informed consent forms (ICF) and addressing regulatory escalations. You will build and manage lab databases to meet specific clinical trial needs, monitoring the acquisition and testing of diverse sample types, including human tissue, whole blood, plasma, and serum.
A significant portion of your time will be dedicated to operational planning and vendor oversight. This includes assessing vendors, forecasting costs and timelines, reviewing invoices, and preparing Requests for Proposals (RFPs). You will guide vendors, collaborators, and clinical sites on best practices for sample collection, processing, shipping, and storage. Additionally, you will work with data management leads to define how sample and testing data are captured, blinded, and transferred, ensuring seamless data flow from vendors to internal systems.
Qualified candidates will be considered for this remote opportunity. The selection process focuses on identifying individuals with a strong background in clinical research lab study management who can demonstrate the ability to work independently while contributing to group initiatives.
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Work model: Remote
Skills: Clinical Trials, Clinical Databases, Laboratory Sample Management, Microsoft Applications.
Education: Bachelor's degree in a life science required; Nursing qualification (Bachelor's level) required.
2925, H Street, Marshall School, East Sacramento, Sacramento, Sacramento County, California, 95816, United States
Sacramento, California
Laboratory sample management experience
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