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Clinical Trial Assistant

Employer
Labcorp
Location
Madrid, Spain
Salary
Competitive
Start date
21 Jul 2021
Closing date
30 Jul 2021

View more

Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details


We have a new sponsor dedicated position at Covance by Labcorp

As a Clinical Trial Assistant you will:

Assist the Clinical Project Leader and CRA in handling logistics and administrative matters related to a specific study. Participate in the study set up (administrative and logistic tasks): General administrative activities and archiving and filing.

Your main functions:

  • Participate in the study set up (administrative and logistic tasks) including management of the required documents for regulatory submission to Health Authorities (HHAA), Ethics Committee (EECC): correspondence, CTA forms, clinical study documents, templates, etc
  • Give support preparing required documents for monitoring visits.
  • Preparation of Investigator Study File.
  • Send documentation / material to sites/investigators upon request of CPL/CRA.
  • Participate in local filing and local archiving.
  • Collaboration, with the rest of the Monitoring Team, in the Investigators Meeting and related events.
  • Participate in logistic aspects of CRFs, SAEs and reports.
  • Provide internal and external communication support.
  • If applicable, provide support to the monitoring activities when applicable (i.e.: co-monitoring with CPL/CRA, administrative closure of the site, ...).
  • Management of DILs (according to periodical distribution of molecules among CPAs).
  • Courier management.
  • CSU purchasing for special trial site supplies.
  • Post the clinical trial financial agreement and subsequent goods receipt in eBUY
  • Support in investigators payments
  • Follow-up of invoices in eBUY and EasyInvoices
  • Technical handling of changes in personnel (lay-out, placement, equipment...)
Education/Qualifications:
  • Advanced level of English
Experience:
  • +1 year of experience as a CTA or similar role
  • Experience with eTMF ideally Veeva Vault
  • Solid background supporting clinical trials as a CTA or similar role in another CRO or Pharmaceutical company.
  • Based in Madrid ideally, otherwise Barcellona.

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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