Senior Clinical Research Associate (Oncology)

TL;DR

Senior Clinical Research Associate (Oncology): Managing study sites and project teams for clinical research studies with an accent on patient safety, data quality, and regulatory compliance. Focus on conducting site visits, managing site start-up procedures, and ensuring ICH-GCP adherence in oncology and rare disease trials.

Location: Remote, China (60-70% travel required)

Company

hirify.global is a specialized CRO that integrates clinical trial execution with deep scientific knowledge and advanced data sciences, focusing primarily on Oncology and Rare Diseases.

What you will do

• Oversee all aspects of study site management to ensure patient safety and high data quality.
• Conduct pre-study, initiation, routine monitoring, and close-out visits in accordance with protocols and local laws.
• Manage site start-up procedures, including feasibility, recruitment, and regulatory document collection.
• Perform investigational product (IP) inventory, reconciliation, and security reviews.
• Perform data review activities, including remote EDC CRF review and query resolution.
• Identify and process Serious Adverse Events (SAE) and escalate site risks to management.

Requirements

• Bachelor's degree in a business, scientific, or healthcare discipline.
• Minimum of 2 years of on-site monitoring experience.
• Minimum of 1 year of oncology experience.
• Experience with Global Clinical Trials.
• Fluency in English communication, both verbal and written.
• Must be based in China and available for 60-70% travel.

Nice to have

• Solid overall experience in clinical research.
• Excellent organizational skills.
• Ability to work efficiently in a remote work environment.

Culture & Benefits

• Opportunity to work with cutting-edge technologies in life sciences.
• Focus on high-impact areas like oncology and rare diseases.
• Professional environment emphasizing scientific expertise and operational scale.
• Equal Opportunity Employer commitment.