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.
Genomic Medicine Scientist II - Biomarker Data Steward and Sample Lifecycle Management (East Coast)
Job ID R0000029992Are you passionate about advancing genomic medicine and making a real impact on clinical trials?
Join our dynamic team as a Genomic Medicine Scientist II (Biomarker Data Steward and Sample Lifecycle Management) and play a crucial role in revolutionizing patient care through cutting-edge genetic and biomarker research.
This exciting role will work in partnership with a large global pharmaceutical client to operationally support the incorporation of genetics and biomarkers into clinical research.
Description of Role & Responsibilities:
Manage set-up, development, and maintenance of biomarker study plans for clinical trials in relevant systems
Support lifecycle management of samples collected as part of clinical trials.
Skills and Experience:
Experience with global clinical trials and associated systems (including LIMS)
Ability to understand and apply company policies and procedures to individual work
Strong attention to detail
Must be self-motivated, able to work independently and as part of a team
Ability to manage multiple assignments 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 client tools and databases used to support role responsibilities
Experience with MS Office Suite
Excellent communication skills, both written and oral
Educational Requirements: BA/BS and at least 5 years of relevant experience. Advanced degrees highly desirable.
East Coast candidates are highly preferred, but strong candidates living in CST with a willingness to work East Coast hours will also be considered.
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