Eva Massamiri
About Eva Massamiri
Eva Massamiri is a Clinical Trial Associate with extensive experience in the pharmaceutical industry, currently working at AstraZeneca and TFS Trial Form Support since 2017. She has held various roles in clinical trials and contract administration, contributing to her expertise in the field.
Work at TFS HealthScience
Eva Massamiri has been employed at TFS Trial Form Support as a Clinical Trial Associate since 2017. In this role, she contributes to the management and oversight of clinical trials, ensuring compliance with regulatory requirements and organizational standards. Her experience in this position spans over seven years, during which she has developed a strong understanding of clinical trial processes and methodologies.
Current Role at AstraZeneca
Since 2017, Eva Massamiri has also been working at AstraZeneca as a Clinical Trial Associate. In this capacity, she is involved in the planning and execution of clinical trials, focusing on the development of new therapies. Her tenure at AstraZeneca has allowed her to gain valuable insights into the pharmaceutical industry and the intricacies of clinical research.
Previous Experience at Servier
Prior to her current roles, Eva Massamiri worked at Servier as a Contract and Budget Administrator from 2017 to 2018. During her one-year tenure, she was responsible for managing contracts and budgets related to clinical trials, which provided her with essential skills in financial oversight and project management.
Background in Intellectual Property
Eva Massamiri began her career as a Paralegal Trademark Assistant at Zacco - 360° Intellectual Property from 2006 to 2007. This role involved assisting with trademark registrations and intellectual property matters, laying a foundation for her analytical and administrative skills in the legal field.
Long-Term Role at ICON plc
Eva Massamiri has been working at ICON plc as a Clinical Trial Assistant since 2007. With over 17 years of experience in this position, she has developed expertise in supporting clinical trial operations, including participant recruitment, data collection, and compliance monitoring. Her extensive background in clinical trials enhances her contributions to the industry.