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Clinical Research Associate
医疗健康·医疗科技
Clinical Research Associate (CRA) oversees trial execution, ensures data integrity and compliance, and coordinates sites, sponsors, and regulators.
Daily work
- 01Review clinical trial protocols and case report forms
- 02Conduct on-site monitoring visits to verify source data
- 03Write monitoring reports and track issue resolution
- 04Communicate with investigators, CRCs, and sponsors on progress
- 05Assist in handling adverse event and serious adverse event reports
Ability requirements
Hard skills
- Proficient in GCP and ICH guidelines
- Knowledge of full clinical trial lifecycle
- Basic data analysis and statistical software (e.g., SAS, SPSS)
- Medical English reading and writing
- Electronic Data Capture (EDC) system operation
Soft skills
- Excellent communication and coordination
- Strong attention to detail and accountability
- Stress tolerance and time management
- Balance between teamwork and independence
- Logical thinking and problem-solving
Best suited for
Ideal for detail-oriented, organized individuals with strong communication and coordination skills, who can handle frequent travel and fast-paced project management.
Less suited for
Not suitable for those who dislike repetitive documentation, resent business trips, or have low stress tolerance.
Salary (monthly)
Pre-tax estimate, tier-1 cities with social insurance · reference only
Profile
MBTI Fit
Resume examples for this role
Disclaimer: Salary figures on this page are estimated pre-tax monthly pay for positions with social-insurance contributions in China's tier-1 cities; other cities are converted using regional coefficients. Dimension scores and MBTI fit are editorial estimates, provided for reference only, and do not constitute any promise or advice.