Description
Syneos Health is seeking a Senior Clinical Research Associate (CRA) to work remotely from Argentina.
As a Sr CRA, you will conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices. You will develop tools, procedures, and processes to ensure quality monitoring, and contribute to the design, implementation, and delivery of processes, programs, and policies.
Key responsibilities include:
- Conducting on-site and remote monitoring of clinical research studies
- Developing monitoring plans, checklists, and standard operating procedures
- Providing expert input and feedback during development and review stages
- Directing the work of lower-level professionals and managing processes and programs
- Ensuring trials are conducted in accordance with regulatory requirements and company standards
- Providing guidance and support to clinical research teams
- Maintaining accurate and timely documentation of monitoring activities
- Identifying and resolving issues related to clinical trial conduct
- Collaborating with cross-functional teams to ensure successful trial execution
Requirements:
- Bachelor's degree in a related field
- Minimum of 5 years of experience in clinical research monitoring
- In-depth knowledge of clinical trial processes and regulations
- Strong analytical and problem-solving skills
- Excellent communication and interpersonal skills
- Ability to work independently and as part of a team
Preferred certifications:
- Certified Clinical Research Associate (CCRA) or equivalent certification
Necessary skills:
- Proficiency in clinical trial management systems and software
- Ability to manage multiple projects and priorities
- Strong attention to detail and organizational skills
- Ability to travel as required for on-site monitoring
- Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements