Role Description

This is a Remote role for a Clinical Research Associate (Consultant) located in Shanghai, China. But monthly 1 or 2 times site visits.

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.

Qualifications

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

The following skills and qualifications would be beneficial:
Experience with regulatory compliance and submission preparation
Familiarity with GCP and ICH guidelines
Certification as a clinical research coordinator or associate

Industry:
Pharmaceutical Manufacturing

Qualification Any Life Sciences Degree
Experience 2+ Years
Job Category CRA
Posted On 8/30/2024
Expires On 9/30/2024