Senior Clinical Research Associate (Sr. CRA)

Adecco

  • Sinyi, Taipei City
  • Permanent
  • Full-time
  • 2 months ago
  • Apply easily
Global CRO companies are hiring experienced CRAs to implement clinical research operations.

Location: North Taiwan

- Our clients are Global CRO companies, providing career development, good packages and benefits.

- Currently our clients are hiring experienced CRAs to implement clinical research operations.

Responsibilities:

- Conduct site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.

- Ensure compliance with SOPs, protocols, ICH/GCP and related regulatory requirements.

- Support inputs to Country/Site Trial Master Files (TMF). Monitor the completeness and quality of Regulatory Documentation.

- Perform site document verification.

- Conduct good collaboration with stakeholders in the company, sites and sponsor(s) and perform excellent communication and problem-solving skills.

Requirements:

- Bachelor’s degree in medical science, pharmacy, nursing or related life science/healthcare discipline.

- 4+ years of global clinical trial experience. Site visit experience is a must.

- Proactive and good interpersonal skills.

- Fluent in English.

For further information, please contact Claire Wei ( ). Thanks and look forwards to hearing from you.

Adecco

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