Allucent
1001 - 5000 employees
💼 Consulting
🏥 Healthcare
📦 Logistics
Consulting • Healthcare • Logistics
Allucent is a leading partner for small and mid-sized biotech companies, offering innovative regulatory and clinical development solutions. With over 30 years of experience, Allucent specializes in therapeutic expertise, clinical pharmacology, regulatory strategy, drug safety, and the pharmacovigilance processes needed to bring new therapies to market. Their comprehensive services address challenges from early-phase drug discovery through clinical trials and post-marketing surveillance, supporting various therapeutic areas such as oncology, infectious disease, neurology, autoimmune diseases, and rare diseases. Allucent's commitment to fostering breakthrough science helps biotech companies navigate the complexities of drug development efficiently and effectively.
Senior Clinical Research Associate, Local Start-Up Specialist
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Allucent
1001 - 5000 employees
💼 Consulting
🏥 Healthcare
📦 Logistics
Consulting • Healthcare • Logistics
Allucent is a leading partner for small and mid-sized biotech companies, offering innovative regulatory and clinical development solutions. With over 30 years of experience, Allucent specializes in therapeutic expertise, clinical pharmacology, regulatory strategy, drug safety, and the pharmacovigilance processes needed to bring new therapies to market. Their comprehensive services address challenges from early-phase drug discovery through clinical trials and post-marketing surveillance, supporting various therapeutic areas such as oncology, infectious disease, neurology, autoimmune diseases, and rare diseases. Allucent's commitment to fostering breakthrough science helps biotech companies navigate the complexities of drug development efficiently and effectively.
📋 Description
• Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits • Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements • Build strong site relationships and act as a primary point of contact • Ensure high-quality data collection • Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety • Perform activities around regulatory affairs, site activation, and study start-up • Travel throughout Ukraine
🎯 Requirements
• Minimum of at least 5 years’ experience leading monitoring activities in complex trials • Experience ideally in oncology or rare disease trials • Strong understanding of ICH-GCP and regulatory guidelines • Clear and confident communication in English and local language • Ability to work independently and manage priorities • Willingness to travel as required
🏖️ Benefits
• Meaningful partnerships with clients • Collaboration with top minds across science, business, and operations • Opportunity to advance pharmaceuticals and biologics • Opportunity to contribute to life-changing treatments and improve patient lives
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