Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Sample Management Specialist (East Coast)
Job ID R0000030078Parexel 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
Due to the location of the Client, East Coast Candidates are strongly preferred; however, strong CST candidates who are willing to work East Coast hours will also be considered.
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