Clinical Laboratory Study Manager - FSP
Not Disclosed•Full-TimeRemote
location_onBeacon Street Mall, Beacon Hill, Boston, Suffolk County, Massachusetts, 02108, United States
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 such as 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 tangible medical applications.
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 technical oversight, you will drive overall project management aligned with the core business strategy, managing the full lifecycle of sample operations including collection, processing, storage, shipping, and transfer.
Your work involves a dynamic mix of operational support, data acquisition, and compliance management. You will liaise with internal stakeholders, such as ICF specialists, to address technical and operational sample-related matters for assigned projects. A significant portion of your time will be dedicated to establishing and overseeing the planning and integration of sample analysis, including exploratory analysis, while managing reporting and billing for study operations.
You will collaborate with Precision Medicine Strategy Leads and scientists to assess vendors, forecast operational costs and timelines, and review invoices to ensure budget alignment. Additionally, you will work directly with data management leads to define how sample and testing data are captured, blinded, and transferred for clinical trials. Providing guidance to clinical teams and sites regarding the collection, storage, and shipping of human samples is a key daily responsibility, ensuring all activities comply with study protocols and applicable Informed Consent Forms (ICF).
Qualified candidates will be considered for employment without regard to legally protected status. The application process involves reviewing your background in clinical research and laboratory sample management to ensure alignment with the 6-8 years of experience required in the academic, CRO, or pharmaceutical/biotech industry.
Work model: Remote
Beacon Street Mall, Beacon Hill, Boston, Suffolk County, Massachusetts, 02108, United States
Boston, Massachusetts
Laboratory sample management experience
Skills: Clinical Trial Management, Clinical Research, Clinical Trials, Clinical Databases, Laboratory Sample Management, Microsoft Applications.
Education: Bachelor's degree in a life science required.
PAREXEL is a global clinical development partner specializing in insights-driven clinical and consulting solutions for the pharmaceutical manufacturing industry. Based in Raleigh, North Carolina, the company collaborates with biopharmaceutical leaders, emerging innovators, and research sites to design and execute patient-focused clinical trials. By combining localized expertise with global regulatory and therapeutic knowledge, PAREXEL aims to improve access to clinical research for patients worldwide. With a workforce of over 22,000 professionals, the organization supports complex healthcare initiatives and streamlines clinical development processes through innovation. Recognized for its patient-centric approach, PAREXEL has received industry accolades including the 2025 Scrip Award for Best Contract Research Organization and the 2024 Fierce Biotech CRO Award for innovative patient research strategies. The company’s commitment to advancing life-changing treatments spans more than four decades of experience in clinical research.
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Experience
6-8 yrs (Senior)
Education
Bachelor's degree in a life science required
Job Type
Full-Time