• The Clinical Research Associate will be responsible for the day-to-day activities associated with clinical trial management, including protocol review and participation in the design and implementation of clinical trials.
• Additionally, the Clinical Research Associate will liaise with clinical operations teams, conduct research, and provide support to the medical/scientific community.

• Strong knowledge and experience in clinical trials and clinical monitoring.
• 2+ years of experience as a CRA
• Demonstrated ability to create, review, and implement clinical trial protocols
• Experience in clinical operations, including site management, monitoring, and data management
• Ability to conduct research, analyze data, and interpret results
• Bachelor's or Master's degree in a related scientific field
• Excellent communication and organizational skills
• Ability to work independently and remotely

• Experience with regulatory compliance and submission preparation
• Familiarity with GCP and ICH guidelines
• Certification as a clinical research coordinator or associate

• Pharmaceutical Manufacturing