Description
Syneos Health is seeking a Sr CRA I - Sponsor dedicated to work from home in Chile.
As a Sr CRA I, you will conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices. You will verify the accuracy and completeness of data collected and ensure adherence to study protocols.
Key responsibilities include:
- Developing and implementing tools, procedures, and processes to ensure quality monitoring
- Contributing to the design, implementation, and delivery of processes, programs, and policies
- Managing and directing the work of lower-level professionals or managing processes and programs
- Ensuring accurate and timely documentation and reporting of clinical trial data
- Collaborating with cross-functional teams to support clinical trial activities
- Identifying and resolving issues related to clinical trial conduct and data integrity
- Providing training and mentorship to junior staff members
Requirements:
- Bachelor's degree in a related field
- Minimum of 3-5 years of experience in clinical research or a related field
- 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 Professional (CCRP) or equivalent certification
Necessary skills:
- Proficiency in clinical trial management systems and software
- Strong organizational and time management skills
- Attention to detail and accuracy
- Ability to manage multiple projects and priorities simultaneously
- Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements