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Careers

At ClinSearch, we are always interested to hear from job seekers with clinical research, medical writing, or biostatistics and SAS programming experience. At a minimum, our staff members have MS/PharmD/PhD in life sciences and speak French and English.
Fluency in an additional language such as Dutch, German, Swedish, Spanish etc. is beneficial when applying for a CRA job due to the pan-European focus of our monitoring department.

As an employer, ClinSearch is committed to offering:

  • Dynamic and truly international work and working environment. We currently have 20 nations represented on the team and most of our projects are international in scope
  • Opportunities for continued training and development in areas of company needs and individual interests. Regular training in new regulatory and technological developments
  • A flat management structure loosely focused around projects, where everyone can contribute new ideas
  • A beautiful, light and airy open office space at the border of Malakoff and Montrouge, with easy access to both Metro lines 4 and 13
  • Flexible work hours, with core hours 10-16
  • 1 day work from home weekly, confirmed in each individual job offer
  • Support with visa requirements for candidates outside the EU, confirmed in each individual job offer
  • Team buildings and company events

For ongoing evaluations, please send your CV to info@clinsearch.net or contact Ivelina Georgieva to discuss your unique situation: confidentially and in detail.

Specific job offers will be posted when available here and on our LinkedIn page.

OPEN POSITIONS AS OF FEBRUARY 2019

CRA with Danish - Entry level or experienced

We are a European Organization which develops innovative solutions and apps in Clinical Evaluation, Patient-Centered Healthcare Systems, Patient-Reported Outcomes Measures, Assessment of Patient Preferences, Health Market Access and Public Health. We are currently looking for a Clinical Research Monitor/CRA, fluent in Danish, English and French, to join our Clinical Research team. In brief, the successful candidate will have the opportunity to work alongside our experienced CRAs to obtain expertise in the direction in all clinical evaluation and regulatory matters and acquire good working knowledge in the application of ISO guidelines for the development of medical devices and ICH guidelines for the development of medicines.
DAY-TO-DAY JOB DUTIES
  • Monitor clinical sites in France, the UK and Nordic countries
  • Interact with Institutional Review Boards with respect to Protocols, Informed Consent Forms and other documents as required. Act as a secondary liaison between the company and the Institutional Review Board
  • Assist in the development of document templates, relevant Standard Operating Procedures (SOPs) and guidelines
  • Work closely with clinical personnel and the Principal Investigator to ensure that clinical documents are produced to the standard required by Good Clinical Practice (GCP)
  • Ensure accurate and complete documentation of all clinical study source documents and/or forms according to company’s SOP, GCP and other applicable guidelines
  • Conduct all work in compliance with SOP’s, GCP and to observe all regulatory guidelines
  • Compile study documents
  • Perform other work as assigned


QUALIFICATIONS
  • Bachelor’s or Master’s degree in Life Sciences
  • Some initial clinical research or clinical training experience
  • Fluency in Danish, advanced English and French
  • Excellent interpersonal and communication skills
  • Attention to detail, good initiative and ability to work with changing priorities
  • Scientific accuracy
  • Ability to work autonomously
  • Strong customer focus


ADVANTAGES
  • Competitive Salary Package
  • Exempt position
  • Group Insurance Coverages
  • 5 weeks of holidays plus 10 extra days


IF YOU ARE INTERESTED IN THIS CAREER OPPORTUNITY
Please apply now by sending a word document of your CV to reach.us@clinsearch.net.
Read more about our company on https://www.clinsearch.net.

CRA with Swedish - Entry level or experienced

We are a European Organization which develops innovative solutions and apps in Clinical Evaluation, Patient-Centered Healthcare Systems, Patient-Reported Outcomes Measures, Assessment of Patient Preferences, Health Market Access and Public Health. We are currently looking for a Clinical Research Monitor/CRA, fluent in Swedish, English and French, to join our Clinical Research team. In brief, the successful candidate will have the opportunity to work alongside our experienced CRAs to obtain expertise in the direction in all clinical evaluation and regulatory matters and acquire good working knowledge in the application of ISO guidelines for the development of medical devices and ICH guidelines for the development of medicines.
DAY-TO-DAY JOB DUTIES
  • Monitor clinical sites in France, the UK and Nordic countries
  • Interact with Institutional Review Boards with respect to Protocols, Informed Consent Forms and other documents as required. Act as a secondary liaison between the company and the Institutional Review Board
  • Assist in the development of document templates, relevant Standard Operating Procedures (SOPs) and guidelines
  • Work closely with clinical personnel and the Principal Investigator to ensure that clinical documents are produced to the standard required by Good Clinical Practice (GCP)
  • Ensure accurate and complete documentation of all clinical study source documents and/or forms according to company’s SOP, GCP and other applicable guidelines
  • Conduct all work in compliance with SOP’s, GCP and to observe all regulatory guidelines
  • Compile study documents
  • Perform other work as assigned


QUALIFICATIONS
  • Bachelor’s or Master’s degree in Life Sciences
  • Some initial clinical research or clinical training experience
  • Fluency in Danish, advanced English and French
  • Excellent interpersonal and communication skills
  • Attention to detail, good initiative and ability to work with changing priorities
  • Scientific accuracy
  • Ability to work autonomously
  • Strong customer focus


ADVANTAGES
  • Competitive Salary Package
  • Exempt position
  • Group Insurance Coverages
  • 5 weeks of holidays plus 10 extra days


IF YOU ARE INTERESTED IN THIS CAREER OPPORTUNITY
Please apply now by sending a word document of your CV to reach.us@clinsearch.net.
Read more about our company on https://www.clinsearch.net.

Ingénieur Qualité logiciel

Nous sommes une société européene qui developpe des solutions innovantes dans les domains de recherche clinique, de santé publique, d’économie de santé, et d’apps de santé.
A raison de notre expansion organique, nous cherchons un nouveau collègue pour notre departement informatique.

MISSIONS

Prendre en charge l'ensemble des tests des logiciels, d'établir les scénarios de test, organiser et réaliser leurs exécutions et de synthétiser les résultats
  • Test fonctionnels
    • Tester le bon fonctionnement global
    • Tester sur de multiple environnements (navigateurs, systèmes, devices,...)
  • Test métiers
    • Tester la cohérence entre data/querie
    • Tester la cohérence entre IHM/extraction
  • Test de monté en charge
    • Tester l'application avec un volume de donnée important
    • Vérifier l'absence de fuite mémoire
    • Réaliser des benchmark de performance
  • Test de non-régressions
    • Comparer l'ensemble des tests entre la version N avec la N-1
  • Gestion des tickets d'anomalie ou d'évolution
    • Tester puis valider ou rejeter les tickets
    • Rédiger des tickets pour toutes nouvelles anomalies
Administrer les serveurs d'applications
  • Interne, externe et production
  • Prévenir des anomalies (contrôle des logs)
Helpdesk
  • Régler les problèmes liés au système d’information des collaborateurs)


COMPETENCES TECHNIQUES
  • BAC+2 (BTS, DUT) en Qualité logiciel
  • Linux (Ubuntu)
  • Glassfich/Apache
  • Des notions en JAVA et SQL