Desired profile:
- Life Science graduate
- Moderate clinical research experience in a contract research organization, pharmaceutical, or biotechnology company.
- Clinical research organization (CRO) and relevant therapeutic experience preferred.
- Previous technical and managerial experience in conducting multi-national and/or local clinical trials in a hospital setting, pharmaceutical company, or CRO preferred. Thorough knowledge of regulatory requirements, drug development, and clinical monitoring procedures.
- Demonstrated proficiency with ICH/GCP guidelines. Keen insight, independent judgment, and tactful discretion. Presentation, documentation, and interpersonal skills as well as a team-oriented approach. Proficient computer skills in Word, Excel, PowerPoint, email and Internet. Basic computer skills using MS Project.
- Flexibility and the ability to handle multiple tasks to meet deadlines while delivering high quality work in a dynamic environment.
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