Parexel is looking to hire a Sample Management Specialist with experience in Clinical Trials to support centralized management processes!

This is a remote position and will be exclusively operational and computer based. In this role, you will support sample management by making sure study management plans are correct, overseeing sample chain of custody, and performing quality control and sample reconciliation. In this role, you will also work closely with early phase clinical specialists and scientists, as well as performing study closeout duties.

Description of Role & Responsibilities:

• Support centralized specimen management processes
• Responsible for compliance of specimen activities
• Understand the required assays and associated specimens as defined by protocols
• Ensure study specimen management plans are correct, including all planned specimen chain of custody
• Prepare study manifest templates and assist with specimen-related documents
• Track and reconcile specimens
• Assist with study closeout and final specimen disposition

Skills and Experience:

• Experience with clinical trials and clinical sample management required
• Must be self-motivated, able to work independently and as part of a team
• Ability to manage complex projects under accelerated timelines
• Ability to partner effectively with internal and external teams to achieve results
• Strong issue identification and resolution skills
• Able to learn quickly and be proficient in applicable tools and databases used to support the activities
• Experience with MS Office Suite
• Excellent communication skills, both written and oral

Educational Requirements: BS and at least 3 years of related experience