Advance your career as a Clinical Research Associate II in a fast-evolving CRO, specializing in dermatology. Monitor clinical trials while ensuring adherence to ICH-GCP and regulatory standards.

With 2-5 years of hands-on experience in clinical monitoring, you'll conduct vital site qualifications and maintain quality throughout the research process. Your ability to prioritize tasks and communicate effectively will be essential in building relationships and meeting recruitment goals. Work autonomously while making a meaningful impact in this focused therapeutic area.

Key Responsibilities:
• Monitor and evaluate clinical trial sites
• Initiate and finalize site visits as per protocols
• Compile reports and maintain study documentation
• Build effective relationships to meet study targets
• Ensure accuracy in data collection and regulatory compliance

Requirements:
• Relevant B.Sc. or nursing degree
• Proven C...