ICON Clinical Research

Senior CRA - €7,000 sign on bonus available

4 days left

Location
Paris
Salary
Competitive
Posted
22 Apr 2021
Closes
22 May 2021
Ref
JR073588
Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
Senior Clinical Research Associate

At ICON, it's our people that set us apart.

Are you a dynamic, organized, rigorous Senior CRA, and want to join a dynamic team in France?

Location: Home based or office based (Paris)
Job Field: Clinical Operations
Employment Status: Permanent

About ICON:

ICON is a global provider of outsourced drug development and commercialisation solutions and services to the pharmaceutical, biotechnology, medical device and government and public health organisations. With headquarters in Dublin, Ireland, ICON currently, operates in 37 countries and has approximately 13 700 employees. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?

Position summary:

  • You will work within a large-scale, fast-paced international environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate, monitor and close-out investigational sites for clinical studies in phases I to IV, ensuring adherence to applicable SOPs, regulations and principles of ICH-GCP.
  • Manage sponsor generated queries efficiently and responsible for study cost effectiveness
  • Dependent on level of experience you may assist in training and mentoring less experienced CRA's and/or manage CRA's working on international projects


Profile:

  • With a University degree in science or equivalent, you have a minimum of 24 months experience as a Clinical Research Associate on clinical studies, across any therapeutic area for a CRO, Pharma industry or hospital environment.
  • You have a driving license and are available to travel throughout France.
  • Your dynamism, your autonomy, your relationship, your keen sense of organization and your willingness to deliver within required timelines and according to the desired quality, makes you ideally suited to evolve in this function.
  • Fluent in English (written, read, spoken).

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