آریا تینا ژن

منتشر شده 5 سال پیش

Job Description

• Design, develop, and execute protocols for clinical trials that fit with existing regulations and standards. • Manage budget and schedule during clinical trials. • Write study documents, reports, and summaries of adverse events, progress, and employees. • Develop and implement enrollment strategies, monitoring to adjust for dropouts. • Monitor and track progress and obstacles during clinical trial, responding to day-to-day problems. • Liaison with the Trials Steering Committee and Data Monitoring and Ethics Committee with a particular view on compliance with Research Governance, Good Clinical Practice, Data Protection and Ethical Requirements.

Requirements

• Experience in the management and co-ordination of clinical trials; however, appropriate academic and/or vocational qualifications are necessary. • A minimum of a master’s degree in life science or closely related field or Doctorate degree in Medicine or Pharmacy. • Strong communication skills • Professional experience within the pharmaceutical industry • Excellent organization and ability to focus on detail are also essential as all paperwork must be filed systematically and submitted to the appropriate individual or organization

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