Sponsor dedicated Oncology CRA - Netherlands
Syneos Health
6 dagen geleden


WhySyneos Health? Join a game-changing company that is reinventingthe way therapies are developed and commercialized. Created through the mergerof two industry leading companies, INC Research and inVentiv Health, we bringtogether more than 24,000 clinical and commercial minds to create a better,smarter, faster way to get biopharmaceutical therapies into the hands ofpatients who need them most.

Evolve in a global company that is always lookingfor ways to work smarter and more efficiently as the only fully integratedBiopharmaceutical Accelerator.

You'll be supported with comprehensive resourcesbased on today's emerging technologies, data, science and knowledge - insteadof practices from the past.

Teaming with some of the most talentedprofessionals in the industry, you'll gain exposure and work in a dynamicenvironment to over-deliver and outperform.

A career with Syneos Health meansyour everyday work improves patients’ lives around the world.

We arecurrently looking to strengthen our FSP 360 team in the Netherlands and areseeking a Single Sponsor Clinical Research AssociateOncology to be based at our client’s office in Utrecht or homebased.

A brief summary of duties you will beinvolved in :

  • Monitoringoncology clinical trials and participating in all types of site visits ensuringadherence to Good Clinical Practices, investigator integrity and compliancewith all study procedures
  • DataHandling, Reporting, Tracking and administrative tasks
  • Performingmanagement of study site activities to ensure the integrity of clinical data,in adherence to all applicable regulatory guidelines.
  • Qualifications

    Skills and attributes :

    To succeed in this role you will need the following skills / experience :

  • Education- BS / BA or equivalent with solid clinical trial monitoring experience,demonstrating successful performance of CRA position
  • Previousnominal practical experience in conducting clinical pharmaceutical researchstudies in a hospital setting, pharmaceutical company or CRO in oncology area
  • Basicunderstanding of SOPs, WIs, FDA, and local regulations as well as ICH GCPguidelines
  • NativeDutch speaker, and a good command of written and spoken English language
  • Whathappens next :

    If your application is successful you will be contacted by one of our dedicatedrecruiters who will arrange a suitable date and time to speak to you furtherabout this opportunity.

    Tasks, duties, and responsibilities as listed in this jobdescription are not exhaustive. The Company, at its sole discretion and with noprior notice, may assign other tasks, duties, and job responsibilities.

    Equivalent experience, skills, and / or education will also be considered soqualifications of incumbents may differ from those listed in the JobDescription.

    The Company, at its sole discretion, will determine whatconstitutes as equivalent to the qualifications described above.

    Further,nothing contained herein should be construed to create an employment contract.

    Occasionally required skills / experiences for jobs are expressed in brief terms.Any language contained herein is intended to fully comply with all obligationsimposed by the legislation of each country in which it operates, including theimplementation of the EU Equality Directive, in relation to the recruitment andemployment of its employees.

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