Clinical Laboratory Study Manager - FSP
Not Disclosed•Full-TimeRemote
location_on1463, West Indianhead Drive, Tallahassee, Leon County, Florida, 32301, 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, storage, and final destruction. You will act as a key liaison between internal stakeholders and external vendors, including 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 vendor relationships, forecasting operational costs, reviewing invoices, and managing the setup of lab databases to meet specific trial needs. You will also provide guidance and training to vendors, collaborators, and clinical sites on best practices for sample collection, processing, and shipping, ensuring compliance with study protocols and informed consent documents.
Work location
Work model: Remote
1463, West Indianhead Drive, Tallahassee, Leon County, Florida, 32301, United States
Tallahassee, Florida
Key Responsibilities
- check_circleAssess vendors, forecast operational costs, and review invoices to align with budget plans
Similar Job Opportunities
Skills, education and keywords
Skills: Microsoft Applications, Clinical Trials, Clinical Databases, Laboratory Sample Management.
Education: Bachelor's degree in a life science required; Nursing qualification (Bachelor's level) 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
Day-to-day, the Clinical Laboratory Study Manager - FSP at Parexel will assess vendors, forecast operational costs, and review invoices to align with budget plans; prepare rfps and review bids and sows for sample and testing related items; monitor acquisition and testing of clinical trial samples including human tissue and blood products; and guide vendors and clinical sites on sample collection, processing, shipping, and storage protocols.
What are the requirements for this Clinical Laboratory Study Manager - FSP role?expand_more
To qualify for the Clinical Laboratory Study Manager - FSP at Parexel position, applicants should have: Bachelor's degree in life science, nursing, or relevant field; 6-8 years direct clinical research lab study management experience; Working knowledge of clinical trials and clinical databases; and Experience with Microsoft applications.
Where is the Clinical Laboratory Study Manager - FSP role at Parexel located?expand_more
Clinical Laboratory Study Manager - FSP at Parexel is based in 1463, West Indianhead Drive, Tallahassee, Leon County, Florida, 32301, United States. This is a remote role.