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Clinical Trials Assistant

Arya Tina Gene Tehran

Posted 9 months ago

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

-Minimum of a Master’s degree in life science or closely related field or Doctorate degree in Medicine or Pharmacy -Experience in the management and co-ordination of clinical trials; however, appropriate academic and/or vocational qualifications are necessary -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

Job Category:

Healthcare - Nursing

Quality Control, QA & Inspection

Product Development, Research & Development (R&D)

Employement type:

Job Category:

Healthcare - Nursing

Quality Control, QA & Inspection

Product Development, Research & Development (R&D)

Employement type:

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