Clinical Research Associate

The role

Main responsibilities

• 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.
• Haemophilia trial experience is must along with monitoring experience Haemophilia study .
• You’re an experienced CRA ready to take the next step with a company that truly values your expertise and independence. You thrive in an agile, collaborative environment and want to be part of a team making a real impact.
• Experience leading monitoring activities in complex trials, ideally in oncology or rare disease with a minimum of at least 5 years’ experience.
• Strong understanding of ICH-GCP and regulatory guidelines .
• Comfortable working independently and managing priorities.
• Willingness to travel, as required.

Benefits of working at Allucent include

• Comprehensive benefits package per location
• Competitive salaries per location
• Departmental Study/Training Budget for furthering professional development
• Flexible Working hours (within reason)
• Leadership and mentoring opportunities
• Participation in our enriching Buddy Program as a new or existing employee
• Internal growth opportunities and career progression
• Financially rewarding internal employee referral program
• Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
• Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees.

About Allucent

Disclaimers