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Initiation Clinical Research Associate- FRENCH SPEAKING

Argentina - Buenos Aires - Buenos Aires Date posted 09/09/2020 Job ID 62616BR

Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction.

As a CRA at Parexel, you‘ll be joining a team with a wide variety of experiences and knowledge. We’re looking for people like you to take the initiative to do things better and smarter—people who want to grow personally and professionally. We recognize and uphold the importance of all people, the way we do things, our quest for innovation, and most importantly, our patients.

  • Full Time
  • Level: Mid
  • Travel: Yes
  • Glassdoor Rating 3.5

Success Profile

Check out the top traits we’re looking for and see if you have the right mix.

  • Innovative
  • Problem-Solver
  • Communicator
  • Tech-Savvy
  • Confident
  • Independent

"The harmonious environment at Parexel contributes to our success; the great collaboration helps to achieve the goals as one team, and to keep positivity, interest and development alive."

Nicla – Sr Clinical Research Associate


  • Global Impact

    We are one truly global team working together to propel each client´s journey ahead faster.

  • Balance

    We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.

  • Collaboration

    Work with industry leaders and subject matter experts.

  • Freedom

    The ability to innovate, ask “what if” and try new solutions without fear of failure.

  • Variety

    Opportunities to work on multiple accounts – never boring!

  • Compensation

    Competitive salaries and bonus structure based on individual metrics.


Working from our office location in Buenos Aires, as an Initiation Clinical Research Associate (ICRA) you will be the direct point of contact with assigned sites and accountable for quality and delivery during the start-up phase. Duties will include Preparation, negotiation, and facilitation of Confidentiality Agreements (CDA), Clinical Site Agreements (CSAs) and any amendments, Informed Consent Forms (ICF); Conduct remote Qualification Visits (QVs), Update and maintain appropriate Clinical Trial Management systems (CTMS) in a timely manner.

To be considered for this opportunity you must have clinical trials experience as a CRA, study nurse or site coordinator ideally with a university degree in a health-related discipline. Understanding of GCP and relevant regulations plus knowledge of submissions and ICF customizations is expected. This is a virtual team environment and your strong interpersonal and communication skills will help you to succeed. Fluency in English and FRENCH is required as you will support sites in Canada.


  • Significant regulatory and/or site experience in clinical trials
  • Educated to degree level preferred (biological science, pharmacy or other health-related discipline preferred), nursing or other relevant qualification/experience
  • Sound awareness of all relevant regulations, including GCP
  • Fluency in English and FRENCH is required

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