This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies. Find out more here.

Close Message for pharmaceutical industry jobs
NonStop Recruitment is dedicated to putting job seekers looking for pharmaceutical industry jobs in touch with recruiters and employers.

Similar jobs you may be interested in:

Madrid - CRO Data Manager - Biotech (HomeBased)
CRA - Personal CRO
Madrid - CRO Data Manager - Biotech (HomeBased)
CRA II / Senior CRA - Pharma - Paris
Madrid - CRO Data Manager - Biotech (HomeBased)

To receive a FREE weekly email alert of all the latest pharmaceutical industry jobs added to our database enter your email address below.

Submit | Tell me more...

Sister sites:
Our sister site Our sister site
Partner sites:

At Burntsky Limited we work with a number of third parties in order to maximise the reach of the jobs posted with us including but not limited to:

JooblePartner Jooble
UK Jobs
Science Jobs

Job Details
back Back    save job Save Job      apply for job Apply Online      contact recruiter Contact Recruiter            print Print

Madrid - Clinical Data Manager - HomeBased

Business Type: Clinical Research Organisation
Job Type: Clinical Research Associate (CRA)
Job Level: Experienced (non manager)
Position: Full Time
Location: Italy
Reference: AL.249065.2
Closing Date: 07/07/20
Job Details:

A permanent position for you if you like to be in control of your time and manage the information that your teams and you will work with along the research projects.

Among your responsibilities:

  • Implementation and supervision of data management activities.
  • Provide adequate sponsor oversight to data management CRO''s or external data providers
  • Inputs into the data capture tools for a clinical study, including the eCRF and ePRO.
  • Develops and manages the execution of the validation and integration plans, including the validation plan, data set definition and external data sources.
  • Collaboration in creating offers and participating in bid defence meetings.

Key Requirements:

  • At least 2 years of experience in all relevant clinical data management activities in clinical trials.
  • Fluent level of English.
  • Fluent level of Spanish.
  • Experience in leading CDM activities on trial level and managing and supervising external CROs / vendors.
  • Eligible to work in the EU.
  • Good knowledge of MedidataRAVE.
  • An ability to multi-task, under pressure on tasks with varying degrees of difficulty.

Does it feel like the role that you''ve been looking for? Forward us your updated CV at or call us at: +41 43 508 0817 Extension: 3347 and ask for Alejandro Lopez to talk more about it.

NonStop Consulting Posted by:: NonStop Consulting (View all our vacancies)
Unless otherwise stated, if applying for a job, you must ensure that you are already authorised to work in the country in which the job is based
Posted: 30/06/2020 | NPJ Ref: 255730
line graphic

Compatible with:

JobMate   Broadbean   Idibu

Site optimised for Internet Explorer 8+ / Firefox 3+
View a complete Jobs Listing

Credit cards image