In House CRA

Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that’s shaping the future of healthcare and science.

R&D Partners is seeking an In-House Clinical Research Associate (CRA) to support the successful execution of global clinical trials. In this role, you will coordinate regulatory and trial documentation, assist with site activation, and ensure that all clinical records are accurate, complete, and ready for inspection throughout the study lifecycle. You will work closely with clinical study teams, research sites, and other stakeholders to ensure smooth operations, compliance with regulations, and timely achievement of study goals.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Help manage clinical trial activities, including starting, maintaining, and closing studies.
• Organize and maintain essential regulatory documents to meet compliance standards.
• Assist with submitting documents to ethics committees and track approvals.
• Work with research sites to prepare and customize consent forms and other required documents.
• Collaborate with internal teams to ensure smooth study execution.
• Build strong relationships with research sites and provide guidance on processes and requirements.
• Keep clinical trial systems updated with accurate and complete documentation.
• Monitor study progress, identify potential issues, and suggest solutions.
• Support quality checks, audits, and inspections by ensuring all documentation is ready and compliant.
• Follow all relevant regulations and company policies.

Key Skills and Requirements:

• Background in life sciences, nursing, pharmacy, or a related field.
• Experience in clinical research, site activation, or regulatory documentation.
• Knowledge of clinical research regulations such as ICH-GCP, ISO 14155, MDR, and GDPR.
• Strong organizational skills to manage multiple tasks and priorities.
• Excellent communication and teamwork abilities.
• Attention to detail and commitment to high-quality documentation.
• Familiarity with clinical trial management systems (e.g., CTMS, eTMF) and Microsoft Office tools.
• Problem-solving skills and ability to work independently.

Salary:

• $45 to $50 per hour.

For more information, please contact Antonia Ray.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/