Clinical Laboratory Study Manager - FSP
Not Disclosed•Full-TimeRemote
location_on6317, West Markham Street, Little Rock, Big Rock Township, Pulaski County, Arkansas, 72205, United States
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 effective medical treatments.
In this capacity, you will partner closely with project managers from central and specialty labs, offering 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, ensuring seamless operations from sample collection and processing to storage, shipping, and data transfer.
Day in the Life
Your work involves a dynamic mix of operational support, compliance, and strategic planning. You will liaise with internal stakeholders, including Informed Consent Form (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 flow of sample analysis, including exploratory analysis, while managing reporting and billing for study operations.
You will also collaborate with Precision Medicine Strategy Leads and scientists to assess vendors, forecast operational costs, and review invoices to maintain budget alignment. On the data front, you will work 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 collection, storage, and shipping of human samples, ensuring all activities comply with study protocols and applicable informed consent forms.
Hiring Process
Qualified candidates will be evaluated based on their clinical research experience, knowledge of clinical trials and databases, and ability to work independently within a matrixed organization. The selection process focuses on identifying professionals who can resolve problems spontaneously and contribute effectively to group initiatives.
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
6317, West Markham Street, Little Rock, Big Rock Township, Pulaski County, Arkansas, 72205, United States
Little Rock, Arkansas
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
Similar Job Opportunities
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.
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 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 6317, West Markham Street, Little Rock, Big Rock Township, Pulaski County, Arkansas, 72205, 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.
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.