Description
Syneos Health is seeking a CRA II - Single Sponsor based in Bucharest. As a CRA II, you will conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.
Responsibilities:
- Conduct on-site and remote monitoring of clinical research studies
- Develop and implement tools, procedures, and processes to ensure quality monitoring
- Contribute to the design, implementation, and delivery of processes, programs, and policies
- Manage defined components of projects or processes within the area of responsibility
- Ensure accurate and timely documentation of monitoring activities and findings
- Collaborate with cross-functional teams to support clinical trial operations
Qualifications:
- Bachelor's degree in a related field or equivalent experience
- Minimum of 2-4 years of experience in clinical research monitoring
- Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements
- Excellent communication and interpersonal skills
- Ability to work independently and manage multiple priorities
- Proficiency in using clinical trial management systems and other relevant software
Certifications:
- Certified Clinical Research Associate (CCRA) or equivalent certification preferred
Necessary Skills:
- Attention to detail and strong analytical skills
- Problem-solving abilities and critical thinking
- Ability to work effectively in a team environment
- Strong organizational and time management skills
- Proficiency in Microsoft Office Suite