Remote Clinical Lab Study Manager Biomarker Trials

Parexel; Honolulu (HI); On-site; USD 90,000 - 130,000; Full time

Job summary

Parexel in Honolulu seeks an experienced Clinical Operations professional to coordinate sample management and data flows across Precision Medicine Strategy, DM, SKDL and CLPM groups. Role ensures quality samples and data support biomarker evaluation and translation of science to medicine.

Requires 6–8 years clinical research, bachelor’s in life sciences, strong project management and communication, and ability to liaise with CROs and vendors to resolve sample-related queries.

Qualifications

• 6–8 years clinical research experience with academic, CRO or pharmaceutical/biotech industry.
• Working knowledge of clinical trials and clinical databases.
• Laboratory sample management experience is a plus.

Responsibilities

• Supports individual clinical study teams for technical and operational sample-related matters by liaising with internal stakeholders.
• Establishment, oversight, planning and integration of collection, processing, storage, shipping and transfer of samples and data, including reporting/billing.
• Liaises with Precision Medicine Strategy Leads and other scientists re vendors, forecasts sample operational costs, timelines and reviews invoices.
• Works with the data management lead to determine how sample and testing data will be captured, blinded and transferred for clinical trials.
• Provides guidance on collection, storage and shipping of samples, ensures protocol and ICF compliance, documents sample transfers.
• Keeps training, timesheets, expense reports, CV updates and maintains relationships across lines to support portfolio delivery.

Skills

Excellent communication

Project management

Independent work

Interpersonal skills

Microsoft Office

Education

Bachelor's degree in life science

Tools

Microsoft Office Suite

Job description

Parexel in Honolulu seeks an experienced Clinical Operations professional to coordinate sample management and data flows across Precision Medicine Strategy, DM, SKDL and CLPM groups. Role ensures quality samples and data support biomarker evaluation and translation of science to medicine.

Requires 6–8 years clinical research, bachelor’s in life sciences, strong project management and communication, and ability to liaise with CROs and vendors to resolve sample-related queries.