Project Manager Medical Devices - Flexible location EMEA - "CRO Medical Device Project Management e

Employer
Covance
Location
Maidenhead, , United Kingdom
Salary
Competitive
Closing date
7 Oct 2020

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Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
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Job Overview:
Project Manager - Medical Devices - candidates must have Medical Devices Project Management experience working for a Cinical Research Organisation.

The Project Manager is responsible for the day−to−day cross−functional operations of the assigned study or studies for one or more clients. As the team leader, the Senior Project Manager will ensure assigned studies are delivered successfully, on−time, within budget, according to client expectations and with the highest level of quality possible. The Senior Project Manager may manage any combination of the following: single or limited services study or a small regional cross−functional study. Furthermore, a Senior Project Manager may also manage a portion of a larger global study within a given geographical region (i.e. North America, Western Europe, etc.).

Duties & Responsibilities:

Manage, lead and motivate cross-functional project teams, facilitating the team's ability to complete their responsibilities in accordance with project contracts, contract amendments, applicable regulatory, GCP and SOP requirements as well as company policies and procedures

You shall function as the primary liaison between client, third party vendors and the Chiltern project team for project issues

Developing and maintaining project metrics, timelines, budget and deliverables including project plans, trackers and tools for assigned projects

You must proactively manage project budgets, including scope and scope changes, costs, forecasts and margin evaluations

Manage day-to-day operational aspects of assigned projects including third party vendor activities

#LI-NC1
Education/Qualifications:
A successfully completed university degree preferably in science, nursing or applicable industry-related experience
Experience:

  • Candidates must have Medical Device Project Management experience working in a CRO setting.
  • Working knowledge of local regulatory requirements and GCP/ICH guidelines or ISO guidelines
  • Demonstrate good presentation skills
  • Proficiency in Microsoft Office and familiarity with standard project management tools/applications
  • Fluent in English and local language (written & spoken)

 


THERAPEUTIC FOCUS:

Experience in Device/Cardiac-Device is needed.

Additional information:

Office or home based as appropriate

20% travel availability nationally and potentially internationally clients, attendance at conferences and presentations

No freelance applications or agency enquiries will be considered

 

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Join our growing team and discover your extraordinary potential


We are recognized as a leader in drug development because of our exceptional people. At Covance, we embrace and celebrate the different strengths, experiences and perspectives of our 20,000+ team members across the globe. Our team is driven by an energizing purpose to improve health and improve lives. Here, you can play a role in bringing new scientific discoveries to life and make a difference in the lives of millions. And, our comprehensive service portfolio provides the opportunity to explore diverse projects and unique career paths across the drug development spectrum.

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Learn more about our work to improve health and improve lives:

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Contact Us
  • Maidenhead Office Park
  • Westacott Way
  • Maidenhead
  • SL6 3QH
  • United Kingdom
  • Mini-site: Covance
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