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CTA / Senior CTA - sponsor dedicated

Employer
Labcorp
Location
Budapest, Hungary
Salary
Competitive
Start date
30 Apr 2021
Closing date
29 May 2021

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Discipline
Finance / Administration, Administration
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details


Covance FSP are looking to hire a Clinical Trial Administrator/ Senior Clinical Trial Administrator in Hungary.In this position you will be fully dedicated to our sponsor and will be office based.

At Covance, you can redefine what is possible and discover your extraordinary potential within ourFunctional Service Providerteam (FSP).

As a Covance employee dedicated to an FSP project you will bring your specialized discipline to a core team working directly with one sponsor. Whether your specialization is in clinical monitoring, clinical project management, data management, biometrics or pharmacovigilance Covance has an FSP opportunity to match your area of expertise.

Each FSP offers a unique opportunity to be a part of the drug development cycle and see a product through to launch. We have multiple partnerships giving you the variety and the flexibility to stay with sponsors, try a new external secondment or work in house on Covance studies.

With the support of exceptional people and an energized purpose, you'll be empowered to own your career journey with dedicated mentoring, training and personalized development planning.

Core responsibilities:

1) Documenting and tracking study activities using relevant forms and tools, as well as relevant Project Management System.
2) Preparation of study site specific materials in accordance with relevant SOPs
3) Complete minute taking and documentation for sponsor/external or internal teleconferences as requested
4) Setting up and maintaining tracking systems for e.g. study supplies and investigator payments
5) Create and main contact list of study team members, study sites, and external suppliers/contract organizations
6) Support Investigator Meetings.
7) Train and mentor less experienced Clinical Trial Administrators
8) Set up and maintain clinical investigator files and documentation
9) Assist with coordinating study level vendors as requested
10) Organize/prepare for client meetings/teleconferences
11) Liaise with all other departments to ensure the smooth running of the study as needed
12) 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.)
13) Maintain paper trial master file documentation and tracking/archiving as applicable
14) Might be requested to work in a client facing environment
15) Perform other administrative duties as assigned by management
Education/Qualifications:
  • Diploma -Secondary Education or equivalent
Experience:
  • Previous administrative experience or equivalent training/experience in clinical trials
  • Good oral and written communication skills

Company

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.

 

 

 

 

Company info
Website
Location
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom

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