Snr Clinical Trials Administrator - Medical Devices

Employer
Covance
Location
munich, , Germany
Salary
Competitive
Closing date
18 Sep 2020

View more

Discipline
Finance / Administration, Administration
Hours
Full Time
Contract Type
Permanent
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Job Overview:
Senior Clinical Trial Administrator Medical Devices - Office based Munich or Edinburgh

Joining our established team you will have some experience of working within clinical trials but a keen interest in Medical Devices. This role offers excellent career progression with an opportunity in the future to move into an InHouse CRA position.

Main Responsibilities:

  • Documenting and tracking study activities using relevant forms and tools, as well as relevant Project Management System.
  • Preparation of study site specific materials in accordance with relevant SOPs
  • Complete minute taking and documentation for sponsor/external or internal teleconferences as requested
  • Setting up and maintaining tracking systems for e.g. study supplies and investigator payments
  • Support Investigator Meetings.
  • Train and mentor less experienced Clinical Trial Administrators
  • Set up and maintain clinical investigator files and documentation
  • Assist with coordinating study level vendors as requested
  • Organize/prepare for client meetings/teleconferences
  • Liaise with all other departments to ensure the smooth running of the study as needed
  • Provide clerical support to project team (e.g., proof-reading and editing correspondence,large and small documents, mailings, shipment of study files, fax and photocopy documents, assemble study documents, and arrange meetings, etc.)
  • Maintain paper trial master file documentation and tracking/archiving as applicable
Education/Qualifications:
To allow this position to devleop at a future stage into a IHCRA/CRA position, the following quaifications are required.
  • BSc or BA degree in a biomedical or related life science, or nursing qualification
  • Or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
Experience:
  • Previous clinicaladministrative experience or equivalent training
  • Good oral and written communication skills
  • Aptitude for handling and proof-reading numerical data, some spreadsheet software competency
  • Good organizational and time management skills
  • Previous expereince with supporting Clinical Research Associates and Project Managers is essential.
  • German Language skills would be an advantage

Covance Profile Page image

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.

Please visit our Careers Hub

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

https://youtu.be/Wx2wxyLd7no

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