Clinical Laboratory Study Manager - FSP

About the Role

This position serves as a critical bridge between scientific strategy and clinical execution. Working alongside the Precision Medicine Strategy Lead, clinical study teams, and specialized groups including Data Management, Samples, Kits, Data, Logistics (SKDL), and Clinical Laboratory Project Management (CLPM), the 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 practical medicine.

In this capacity, you will partner closely with project managers from central and specialty labs, lending expertise to Clinical Trial Management (CTM) and Contract Research Organizations (CROs). Your focus will be on ensuring samples are collected strictly according to protocol and assisting in the resolution of any sample-related issues or queries. Beyond operational execution, the role involves overseeing overall project management to align with the core business strategy.

Day-to-Day Impact

You will act as a technical and operational liaison for assigned projects, supporting study teams with sample-related matters. This includes collaborating with Informed Consent Form (ICF) specialists to manage trial documents that impact sample testing. You will establish and oversee the planning for sample collection, processing, storage, shipping, and transfer, while managing reporting and billing for study operations.

A key part of your workflow involves assessing vendors, forecasting operational costs and timelines, and reviewing invoices to ensure budget alignment. You will work directly with data management leads to define how sample and testing data are captured, blinded, and transferred for clinical trials. Additionally, you will provide guidance to clinical teams and sites regarding the compliant collection, storage, and shipping of human samples, ensuring all activities adhere to study protocols and applicable ICFs.

Hiring Process

Qualified candidates will be invited to participate in a structured interview process designed to assess technical expertise, problem-solving abilities, and cultural fit. This typically includes an initial screening, followed by deeper discussions on clinical trial management and sample logistics.

Our Culture & Commitment

Parexel is an equal opportunity employer. We are committed to fostering a diverse and inclusive environment where qualified applicants receive consideration for employment without regard to legally protected status, including race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. We value effective relationships across platform lines, Business Units, and Research Units to facilitate effective portfolio delivery.