Remote CRA for Phase I-III Trials – China-based

Medpace; United States; Remote; USD 70,000 - 105,000; Full time

Benefits offered by this job

Competitive compensation

Office-based culture with WFH options

Training programs

Job summary

The company is seeking a full-time, home-based Clinical Research Associate to join our Clinical Operations team in China. This role offers the opportunity to be involved at every stage of drug development, with training provided to carry out duties confidently.

Responsibilities include feasibility visits, source data verification, regulatory document review, drug inventory, and adverse event reporting, plus assessing patient recruitment and retention.

Qualifications

• Bachelor of Science in health-related field (BSN preferred).
• Minimum 2 years of proven CRA experience.
• Broad knowledge of medical terminology and clinical patient management.
• Fluency in local language and English.

Responsibilities

• Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
• Perform source document verification and case report form review;
• Perform regulatory document review;
• Conduct study drug inventory;
• Perform adverse event and serious adverse event reporting and follow-up;
• Assess patient recruitment and retention.

Skills

CRA experience

Education

Bachelor of Science in health-related field

Job description

The company is seeking a full-time, home-based Clinical Research Associate to join our Clinical Operations team in China. This role offers the opportunity to be involved at every stage of drug development, with training provided to carry out duties confidently.

Responsibilities include feasibility visits, source data verification, regulatory document review, drug inventory, and adverse event reporting, plus assessing patient recruitment and retention.