Competitive sign-on bonus considered for qualified candidates
Join Us as a Clinical Research Associate – Make an Impact at the Forefront of
Innovation
We're hiring CRA (Level II) to Sr CRA (Level II) in Madrid and Barcelona, Adecuado
candidates will have at least 2 years experience.
We have successfully supported the top 50 pharmaceutical companies and more than
750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5
years.
As part of our global team, you’ll have the opportunity to perform and
coordinate different aspects of the clinical monitoring and site management
process. As a Clinical Research Associate I, you'll conduct remote or on-site
visits to assess protocol and regulatory compliance and manage required
documentation. You will manage procedures and guidelines from different sponsors
and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a
site processes specialist, you will ensure that the trial is conducted in
accordance with the approved protocol, ICH-GCP guidelines, applicable
regulations, and SOPs to guarantee subjects' rights, well-being, and data
reliability. You will ensure audit readiness and develop collaborative
relationships with investigational sites. Detailed tasks and responsibilities
assigned to your role are outlined in the task matrix.
What You’ll Do:
* Monitors investigator sites with a risk-based monitoring approach: applies
root cause analysis (RCA), critical thinking and problem-solving skills to
identify site processes failure and corrective/preventive actions to bring
the site into compliance and decrease risks.
* Ensures data accuracy through SDR, SDV and CRF review as applicable through
on-site and remote monitoring activities.
* Assess investigational product through physical inventory and records review.
Documents observations in reports and letters in a timely manner using
approved business
📌 CRA (Level II) to Sr CRA (Level II)
🏢 Thermo Fisher Scientific
📍 Madrid
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