Covance

In-house CRA I/ II - sponsor dedicated

Company
Covance
Location
Budapest, Hungary
Salary
Competitive
Posted
30 Apr 2021
Closes
19 May 2021
Ref
10024_65219
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Covance FSP are looking to hire In house CRA I/II. In this position you will be fully dedicated to our sponsor in Hungary, Budapest.

In this role you will be able to gain exposure to contractr negotiation activities and in future grow into CRA position.

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