The CRA II - Chile Home Based position at Syneos Health plays a key role in ensuring the integrity and quality of clinical research studies. You will conduct monitoring activities, support cross-functional teams, and uphold compliance with Good Clinical Practice (GCP) and regulatory requirements, all within a supportive and inclusive global organization.
What You'll Do
- Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms
- Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates
- Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials
- Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues
- Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans
- Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct
What We're Looking For
- 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
- 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
Nice to Have
- Certified Clinical Research Associate (CCRA) or equivalent certification
Technical Stack
- clinical trial management systems
- Microsoft Office Suite
Team & Environment
- Work within cross-functional teams
Benefits & Compensation
- career development and progression
- supportive and engaged line management
- technical and therapeutic area training
- peer recognition
- total rewards program
- Total Self culture – where you can authentically be yourself
- diversity of thoughts, backgrounds, cultures, and perspectives
- a place where everyone feels like they belong
Work Mode
- Home based position in Chile
The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Further, the Company complies with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive.
