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  1. Home
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  5. Clinical Laboratory Study Manager - FSP
Parexel logo

Clinical Laboratory Study Manager - FSP

Not Disclosed•Full-TimeRemote

location_onVermont State Office Building, 118-120;120, State Street, Montpelier, Washington County, Vermont, 05602, United States

Apply Now

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 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 practical medicine.

You will act as a key liaison between project managers, central and specialty labs, and Clinical Trial Management (CTM) teams. Your expertise will be essential in guiding Clinical Research Organizations (CROs) to ensure sample collection strictly adheres to study protocols. Beyond technical oversight, you will manage operational aspects in alignment with core business strategies, from forecasting costs and timelines to reviewing invoices and ensuring budget alignment.

The day-to-day involves resolving complex sample-related queries, establishing workflows for sample analysis and data acquisition, and providing guidance to clinical sites on compliance with study protocols and Informed Consent Forms (ICF). You will also collaborate with internal Human Sample Management teams to ensure rigorous documentation, tracking, and proper disposal of all samples transferred to research groups.

Hiring Process

Qualified candidates will be invited to participate in a structured interview process designed to assess both technical expertise and cultural fit. This typically includes an initial screening, followed by a deeper dive into clinical research experience and operational problem-solving capabilities.

Equal Opportunity

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 location

Work model: Remote

location_on

Vermont State Office Building, 118-120;120, State Street, Montpelier, Washington County, Vermont, 05602, United States

Montpelier, Vermont

Key Responsibilities

  • check_circleAssess vendors and forecast sample operational costs to align with budget plans
  • check_circleProvide guidance to clinical sites regarding sample collection, storage, and shipping compliance
  • check_circleManage sample collection, processing, storage, shipping, and transfer operations per protocol
  • check_circleDetermine how sample and testing data will be captured, blinded, and transferred for clinical trials
  • check_circleCoordinate with clinical study and data management teams to ensure quality sample and data delivery
  • check_circleSupport clinical teams with technical and operational sample-related matters and document liaison
  • check_circleTrack and document all samples transferred to internal research groups for proper usage and destruction
  • check_circleEnsure sample collection and usage comply with study protocols and informed consent forms

Requirements

  • verified6-8 years clinical research experience
  • verifiedBachelor's degree in life science, nursing qualification, or other relevant experience
  • verifiedWorking knowledge of clinical trials and clinical databases
  • verifiedMicrosoft applications

Nice to Have

Laboratory sample management experience

Parexel logo
Company

Parexel

Industry

scientific & qa

View company profilearrow_forwardlanguageWebsite
Quick Overview

Experience

6-8 yrs (Senior)

Education

Bachelor's degree in a life science required

Job Type

Full-Time

Skills Required

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Skills, education and keywords

Skills: Clinical Trial Management, Clinical Research, Clinical Trials, Clinical Databases, Laboratory Sample Management, Microsoft Applications.

Education: Bachelor's degree in a life science required; Nursing qualification or other relevant experience.

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: Assess vendors and forecast sample operational costs to align with budget plans; Provide guidance to clinical sites regarding sample collection, storage, and shipping compliance; Manage sample collection, processing, storage, shipping, and transfer operations per protocol; and Determine how sample and testing data will be captured, blinded, and transferred for clinical trials.
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: 6-8 years clinical research experience; Bachelor's degree in life science, nursing qualification, or other relevant experience; Working knowledge of clinical trials and clinical databases; and 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 Vermont State Office Building, 118-120;120, State Street, Montpelier, Washington County, Vermont, 05602, United States. This is a remote role.
Is this Clinical Laboratory Study Manager - FSP job remote, hybrid, or on-site?expand_more
Parexel has listed this Clinical Laboratory Study Manager - FSP role as remote.
How much experience is required for this Clinical Laboratory Study Manager - FSP role?expand_more
Clinical Laboratory Study Manager - FSP at Parexel typically requires 6–8 years of relevant experience at the senior level.
What skills do you need for the Clinical Laboratory Study Manager - FSP role at Parexel?expand_more
Key skills for Clinical Laboratory Study Manager - FSP at Parexel include Clinical Trial Management; Clinical Research; Clinical Trials; Clinical Databases; Laboratory Sample Management; and Microsoft Applications.
What education is required for Clinical Laboratory Study Manager - FSP at Parexel?expand_more
Educational requirements for this role: Bachelor's degree in a life science required; and Nursing qualification or other relevant experience.
What category does the Clinical Laboratory Study Manager - FSP role belong to?expand_more
Clinical Laboratory Study Manager - FSP at Parexel is part of the scientific & qa job category on Recrutus.
Recrutus

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Search roles by city, category, skill, or job type — explore verified US employers, salary benchmarks, and remote-friendly teams hiring nationwide.

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Clinical Trial Management
Clinical Research
Clinical Trials
Clinical Databases
Laboratory Sample Management
Microsoft Applications
US privacy notice
Accessibility