Syneos Health
Life Sciences
CRAII
“CRA II at Syneos Health. Skills: Clinical research monitoring, GCP guidelines, Regulatory requirements. Conduct on-site and remote monitoring. Ensure compliance with clinical practices”
Industry & Context.
Problem-solving abilities; Critical thinking; Resolve issues
What They're Looking For.
Must Have
Bachelor's degree in a related field or equivalent experience, Minimum of 2-4 years of experience in clinical research monitoring, 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, Attention to detail and analytical skills, Problem-solving abilities and critical thinking, Ability to work effectively in a team environment, organizational and time management skills, Proficiency in Microsoft Office Suite
Nice to Have
Certified Clinical Research Associate (CCRA) or equivalent certification
What You'll Do.
Conduct on-site and remote monitoring
Ensure compliance with clinical practices
Review study protocols
Develop tools and processes for quality monitoring
Create monitoring plans
Contribute to process design and delivery
Participate in SOP development
Manage project components
Coordinate site visits
Ensure accurate documentation
Write monitoring reports
Write follow-up letters
Support clinical trial operations
Work with investigators
How You'll Work.
Team & Collaboration
Collaborate with cross-functional teams; Work with investigators; Work with site staff; Work with other stakeholders
Communication Scope
Excellent communication and interpersonal skills
Process & Methodology
Manage defined components of projects
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