Job Overview
The role of a Senior Clinical Research Associate I involves overseeing the execution of clinical research studies to ensure adherence to widely accepted best practices.
* Conduct thorough on-site and remote monitoring of clinical research studies, encompassing review of study protocols, case report forms, and regulatory documents.
* Develop effective tools, procedures, and processes to guarantee quality monitoring, including creation of monitoring plans, checklists, and standard operating procedures.
* Contribute valuable insights and feedback during the development and review stages of processes, programs, and policies.
* Direct junior staff members or oversee processes and programs, incorporating training and mentoring into their professional development.
This position requires a Bachelor's degree in a related field and at least 5 years of experience in clinical research monitoring. Strong analytical and problem-solving skills, excellent communication and interpersonal abilities, and the capacity to work independently and collaboratively are essential for success.