Clinical Laboratory Study Manager - FSP
Not Disclosed•Full-TimeRemote
location_on948, Spencer Street, Makiki Kai, Honolulu, Honolulu County, Hawaii, 96822, United States
About the Role
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 (DM), 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, managing central and specialty laboratories to ensure samples are collected strictly according to protocol. Your expertise will be vital in resolving sample-related queries and supporting Clinical Trial Management (CTM) and CRO partners.
Beyond operational oversight, you will drive project management aligned with core business strategies. This includes establishing and integrating processes for sample collection, processing, storage, shipping, and data transfer. You will also provide guidance and training to vendors, collaborators, and clinical sites on best practices for sample handling, ensuring compliance with study protocols and applicable informed consent forms.
Work location
Work model: Remote
948, Spencer Street, Makiki Kai, Honolulu, Honolulu County, Hawaii, 96822, United States
Honolulu, Hawaii
Key Responsibilities
- check_circlePrepare RFPs, review bids and SOWs, and assess vendor invoices to align with budget plans
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Similar Job Opportunities
Skills, education and keywords
Skills: Clinical Trials, Clinical Databases, Laboratory Sample Management, Microsoft Applications.
Education: Bachelor's degree in a life science required; Bachelor's degree in nursing qualification required.
Frequently asked questions about Clinical Laboratory Study Manager - FSP at Parexel
What does a Clinical Laboratory Study Manager - FSP at Parexel do?expand_more
A Clinical Laboratory Study Manager - FSP at Parexel is responsible for the following: Prepare RFPs, review bids and SOWs, and assess vendor invoices to align with budget plans; Ensure sample collection and usage comply with study protocols and applicable informed consent forms; Collaborate with data management leads to determine how sample and testing data will be captured and transferred; and Manage central laboratory and specialty vendors to ensure quality sample and data delivery.
What are the requirements for this Clinical Laboratory Study Manager - FSP role?expand_more
Parexel is looking for candidates who meet the following requirements: Bachelor's degree in life science, nursing, or relevant field; 6-8 years direct clinical research lab study management experience; and Working knowledge of clinical trials and clinical databases.
Where is the Clinical Laboratory Study Manager - FSP role at Parexel located?expand_more
Clinical Laboratory Study Manager - FSP at Parexel is based in 948, Spencer Street, Makiki Kai, Honolulu, Honolulu County, Hawaii, 96822, United States. This is a remote role.