Recruitment Consultant at Green Life Science Job Title: Clinical Research Associate (CRA) – Oncology | Remote (Switzerland)
Job Type: Full-Time | Department: Clinical Operations
About Role:
This is a cutting-edge biotechnology company dedicated to developing innovative oncology therapies that target the most aggressive and treatment-resistant cancers. With a robust pipeline of first-in-class and next-generation assets, we aim to transform the standard of care for patients around the world.
We are looking for a Clinical Research Associate (CRA) based in Switzerland to join our growing Clinical Operations team. This is a remote position, with some travel required to support our Swiss clinical trial sites.
Position Overview:
In this role, you’ll be a key player in the execution of our clinical trials, ensuring compliance with regulatory standards and helping bring life-saving oncology treatments to patients. You will work closely with clinical sites, investigators, and internal teams to monitor study progress, ensure data integrity, and maintain high operational standards.
Key Responsibilities:
Perform qualification, initiation, routine monitoring, and close-out visits across oncology trial sites in Switzerland.
Ensure adherence to clinical protocols, ICH-GCP guidelines, Swissmedic requirements, and company SOPs.
Conduct source data verification (SDV) and monitor for protocol deviations, patient safety, and data quality.
Provide ongoing training and support to site staff on study procedures and expectations.
Collaborate with internal stakeholders including Clinical Project Managers, Medical Affairs, and Regulatory teams.
Contribute to risk-based monitoring strategies and continuous process improvements.
Document site visit outcomes and maintain accurate study records and reports.
Qualifications:
Bachelor’s degree or higher in Life Sciences, Nursing, Pharmacy, or related field.
Minimum of 2 years' experience as a CRA, with a strong preference for oncology trial experience (solid tumours or hematologic malignancies).
Demonstrated understanding of early- and/or late-phase oncology trial operations.
Strong working knowledge of GCP, ICH, and Swiss regulatory guidelines.
Fluent in English (written and spoken); German and/or French is a strong asset.
Excellent communication, time-management, and problem-solving skills.
Self-starter with the ability to work autonomously in a fast-paced, remote environment.
Willingness to travel within Switzerland (up to 30%).
What We Offer:
A chance to contribute directly to cutting-edge oncology research with real patient impact.
A collaborative, mission-driven environment where your voice matters.
Remote work flexibility with competitive salary, equity options, and comprehensive benefits.
Career growth opportunities in a rapidly expanding biotech company.
Regular engagement with a global network of experts in cancer research and development.
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