Clinical Lab Study Manager — Biomarker & Data Ops

Parexel; United States; On-site; USD 90,000 - 130,000; Full time

Job summary

Parexel in the United States is seeking an experienced professional to support biomarker and non-biomarker sample operations within clinical trials. You will collaborate with Precision Medicine Strategy Lead, study teams, data management (DM), Samples, Kits, Data, Logistics (SKDL) and Clinical Laboratory Project Management (CLPM) to ensure samples and data are collected per protocol and issues resolved.

Responsibilities include establishing and overseeing collection, processing, storage,

Qualifications

• 6–8 years of clinical research experience with academic, CRO or pharmaceutical/biotech industry.
• Bachelor's degree in life science or related field required.
• Experience with clinical databases and sample management is a plus.

Responsibilities

• Oversee collection, processing, storage, shipping and transfer of samples and data.
• Lead operational sample management and budgeting forecasting.
• Ensure compliance with study protocol and informed consent forms (ICF).
• Collaborate with PMs, DM, SKDL, CLPM, and CROs to support trial delivery.

Skills

Communication

Project management

Organization

Interpersonal skills

Microsoft Office

Education

Bachelor's degree in life science

Tools

Clinical databases

Job description

Parexel in the United States is seeking an experienced professional to support biomarker and non-biomarker sample operations within clinical trials. You will collaborate with Precision Medicine Strategy Lead, study teams, data management (DM), Samples, Kits, Data, Logistics (SKDL) and Clinical Laboratory Project Management (CLPM) to ensure samples and data are collected per protocol and issues resolved.

Responsibilities include establishing and overseeing collection, processing, storage,