Please find attached my CV and PL duly updated for any vacancy related to my educational and professional background. My standard rates per hour are 80€/h. I am currently seeking for new opportunities, I have plenty of availability at the moment of 1.0 FTE. I am open to both freelancer and permanent roles. You can contact me at any time convenient to you, between 10-12 am CET or between 16:30 to 18:30 pm CET in the afternoon. My experience and professional background is focused on the Regulatory Affairs/ Clinical trials & Pharmaco-Vigilance fields, and have over 31 years of experience in regulatory affairs and pharmaceutical development, with specific experience of EU registrations, CMC regulatory requirements and multiple clinical aspects related to successful registration of drug products. I have also deep experience in life-cycle management and significant experience in generic development, ATMP, as well as global clinical development. Clinical trials monitoring according to ICH-GCP, SOP and study protocol: Site Management, identifying, selecting, initiating and closing-out investigational sites and acting as liaison between study site and in-house team. Study Management, working independently and proactively coordinating all necessary activities required to set up and monitor a study. For further details, please see the attached CV and presentation letter duly updated. I am currently looking for a job that matches my experience and professional background, availability for remote working. If you need any further information, do not hesitate to contact me.
Best Regards,
Pilar Corraliza Pérez
Reg. Affairs & Clinical Research Services
pilar.corraliza@regpharma.net
pilarcorralizap@gmail.com
Mobile 727787065------------------------------
María del Pilar Corraliza Pérez
Consultor Senior
Madrid
Spain
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