Was Sie mitbringen sollten
We are looking for a proactive and detail-oriented Clinical Research Associate (CRA) to join our client’s clinical operations team in Basel. In this role, you will monitor clinical trials to ensure compliance with regulatory guidelines, protocols, and good clinical practices (GCP). This is an excellent opportunity for professionals passionate about clinical research and patient safety.
What You’ll Do
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Monitor clinical trial sites to ensure adherence to protocols and GCP
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Conduct site qualification, initiation, monitoring, and close-out visits
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Review site documentation and resolve queries related to data accuracy
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Liaise with investigators, site staff, and internal project teams
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Ensure timely and accurate reporting of trial progress
What You Bring
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Degree in life sciences, nursing, pharmacy, or related field
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2+ years of experience in clinical trial monitoring
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Strong understanding of ICH-GCP and Swiss regulations
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Excellent organizational and communication skills
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Fluency in German is mandatory, English is also required
What We Offer
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A meaningful role in advancing clinical research and patient care
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Competitive salary and travel allowances
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Exposure to cutting-edge studies and therapeutic areas
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Supportive team environment and ongoing training opportunities