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Clinical Trial Coordinator - sponsor dedicated

Employer
Labcorp
Location
Warsaw, Poland
Salary
Competitive
Start date
30 Apr 2021
Closing date
11 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 Clinical Trial Coordinator.In this position you will be fully dedicated to our sponsor in Poland, Warsaw.

At Covance, you can redefine what is possible and discover your extraordinary potential within our Functional Service Provider team (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:

  • Provide clinical support for projects according to sponsor's Standard Operating Procedures, ICH Guidelines and GCP
  • Act as contact for project team and study sites
  • Create, update, track, and maintain study-specific trial management files, tools, and systems
  • Assist CRAs and project team members with one site tasks (e.g. review of Case Report Forms and Study File Notebook, drug accountability) other administrative activities as required (e.g. payments to investigators, correspondence with clients, preparation of status reports, and organization of investigators' meetings)
  • May perform CRF review, query generation and resolution against established data review guidelines, under direct supervision on Covance or client data management systems, as assigned by management
  • Co-ordinate meetings with clients, investigators, and project team, including taking minutes
Education/Qualifications:
  • University/college degree (life science preferred),or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology etc.)
Experience:
  • Previous experience in a similar position will be an asset
  • Good organizational and time management skills
  • Good communication skills, oral and written
  • Exhibit general computer literacy
  • Works efficiently and effectively in a matrix environment
  • Fluent in local office language and in English, both written and verbal

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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