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 clinical trials and manage investigator sites as a contractor with Allucent. Support regulatory affairs, site activation, and compliant study start-up.
Description
- Oversee monitoring for assigned clinical trials, from site initiation through routine visits and close-out.
- Maintain compliance with study protocols, GCP, ICH, SOPs, and applicable regulations.
- Build strong site relationships, serve as a primary contact, and support high-quality data collection.
- Resolve site issues and escalate concerns to protect trial integrity and patient safety.
- Support regulatory affairs, site activation, and study start-up activities.
- Travel throughout Israel.
Requirements
- At least five years of experience leading monitoring activities in complex trials; oncology or rare disease experience is preferred.
- Strong knowledge of ICH-GCP and regulatory guidance.
- Confident communication skills in English and the local language.
- Ability to work independently and manage competing priorities.
- Willingness to travel as required.