-
ID
#29052374 -
Job type
Full Time -
Salary
TBD -
Source
Labcorp -
Date
2021-12-31 -
Deadline
2022-03-01
Global Study Manager Project Manager II - CLS
Maryland, Baltimore, 21276 Baltimore USAVacancy expired!
Job Overview:
Get ready to redefine what’s possible and discover your extraordinary potential. Here at Labcorp Drug Development, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.
Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career.
The Study Manager is responsible for the successful delivery of the study management activities related to companion diagnostic studies in their specific area of the world.
The Study Manager coordinates, plans, organizes and oversees, in his regional location, the completion of administrative and technical tasks during the companion diagnostic study life time in collaboration with the Principal Investigator, the regional laboratory testing site and the various internal departments involved in the deliverables of the study.
The Study Manager ensures the three ways communication with the regional Diagnostic Client in their specific area of the word, the Global Study Manager appointed to the Pharma Sponsor and the regional laboratory operations testing site
.
The Study Manager acts as consultant/Technical Expert in providing recommendations/advice to all parties, a-day-to-day project management oversight by managing, planning and coordinating all projects related as well as maintaining study documentation in accordance with customer expectations and in compliance with regulatory requirements.
In his Global Study Manager role, the Study Manager II is accountable to ensure global consistency of the Diagnostic program across the different laboratory principal investigator testing sites where the diagnostic trial is conducted. He is in charge to coordinate the regulatory aspects with the appropriate operational groups including Medical Affair and Quality Assurance departments
This is FT remote position with possible travel.
Education/Qualifications:
Minimum Required:
- BS degree in Biology, Chemistry or other Life Science; or Medical Technologist degree.
Preferred:
- Computer literate
- Professional certification (ASCP,PMP or other) in area(s) expertise
- Geneva site: qualification by the Foederation Analyticorum Medicilanium Helveticorum (FAMH) or by the Foederation Medicorum Helveticoruma (FMH)
Experience:
Minimum Required:
3-5 years of clinical laboratory experience or customer service experience, preferable in pharmaceutical industry. Experience with multidisciplinary lab background is a plus.
Vacancy expired!
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