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Clinical Research Coordinator/Research Assistant/Research Nurse - Bordeaux

IQVIA

Bordeaux

Sur place

EUR 40 000 - 60 000

Temps partiel

Il y a 12 jours

Résumé du poste

An industry-leading company in Bordeaux is looking for a candidate to support a data extraction project for a clinical trial. This part-time role involves 10 days of work at 8 hours per day, offering complete training. Ideal candidates should have a BS/BA in life sciences, knowledge of clinical trials, and strong IT skills. Excellent interpersonal and organizational abilities are also essential.

Qualifications

  • Relevant work experience in a clinical environment.
  • Ability to establish effective working relationships.
  • Attention to detail is essential.

Responsabilités

  • Support data extraction for a clinical trial.
  • Participate in 10 days of project work.
  • Receive full training for the role.

Connaissances

BS/BA in life sciences or equivalent
Basic knowledge of clinical trials
Basic knowledge of medical terminology
Strong IT competence
Excellent interpersonal skills
Good organizational skills

Formation

BS/BA in life sciences

Outils

MS Windows
MS Office (Access, Outlook, Excel, Word)

Description du poste

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us!

We have an upcoming temporary project for a clinical trial site where you would be responsible for a data extraction project. This part-time role is to support a clinical trial in Bordeaux. There will be 10 days' worth of work, working 8 hours per day. Full training will be given.

We are looking for candidates with the following skills and experience:

  • BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
  • Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
  • Basic knowledge of medical terminology
  • Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
  • Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client
  • Good organizational skills with the ability to pay close attention to detail.

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com

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