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Allucent is a consulting and healthcare partner that helps small and mid-sized biotech companies advance therapies through the drug development process. Its services span clinical development, clinical pharmacology, regulatory strategy, drug safety, and pharmacovigilance, supporting programs from early research and clinical trials through post-marketing surveillance. With more than 30 years of experience and expertise across areas including oncology, infectious disease, neurology, autoimmune conditions, and rare diseases, Allucent works with biotech teams to address the scientific, regulatory, and operational challenges of bringing new treatments to market.
Senior Clinical Research Associate Contractor
Monitor investigational sites across clinical trial phases while maintaining GCP compliance and data quality. Support Allucent’s biopharmaceutical clients with site activation, regulatory activities, and study startup.
Description
- Lead monitoring activities for assigned clinical trials, from site initiation through routine monitoring and close-out visits
- Maintain compliance with study protocols, GCP, ICH, SOPs, and applicable regulations
- Develop trusted site relationships as a primary contact while supporting accurate, high-quality data collection
- Investigate and resolve site issues, escalating risks when necessary to protect trial integrity and patient safety
- Support regulatory affairs, site activation, and study startup activities
- Manage investigator-site relationships and coordinate effectively between sponsors and sites
- Travel throughout Israel
Requirements
- At least five years of experience leading monitoring activities in complex clinical trials, ideally in oncology or rare disease
- Strong knowledge of ICH-GCP and applicable regulatory guidelines
- Confident written and verbal communication in English and Hebrew
- Ability to work independently and manage competing priorities effectively
- Willingness to travel as required
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