Clinical Trials Assistant

Clinical Trials Assistant

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

About Company

50-99 employees

Arya TinaGEN is an Iranian based biopharmaceutical company founded in 2005,aiming manufacturing high-tech products in biotechnology and related fields.as a biotechnology company and advanced R&D center, ATG is intent upon developing biomedicine products for the management of chemotherapy related adverse effects

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