Allucent
Biotechnology • Pharmaceuticals • Science
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.
1001 - 5000 employees
🧬 Biotechnology
đź’Š Pharmaceuticals
🔬 Science
Clinical Research Associate II
Job not on LinkedIn
September 12
🇬🇧 United Kingdom – Remote
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🚫👨‍🎓 No degree required
🇬🇧 UK Skilled Worker Visa Sponsor
Allucent
Biotechnology • Pharmaceuticals • Science
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.
1001 - 5000 employees
🧬 Biotechnology
đź’Š Pharmaceuticals
🔬 Science
đź“‹ 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, acting as a primary point of contact and ensuring high-quality data collection. • Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety. • Activities around regulatory affairs, site activation and study-startup. • Travel throughout The UK to perform monitoring and site activities.
🎯 Requirements
• Experience leading monitoring activities in complex trials, ideally in oncology or rare disease with a minimum of at least 2 years’ experience. • Strong understanding of ICH-GCP and regulatory guidelines. • Clear and confident communicator in English. • Comfortable working independently and managing priorities. • Willingness to travel, as required.
🏖️ Benefits
• Competitive salaries and a comprehensive benefits package • Departmental Study/Training for furthering professional development • Mentoring opportunities • Internal growth opportunities and career progression • Financially rewarding internal employee referral program • Eligibility for our internal employee recognition programs for going above and beyond on projects • Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees
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