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Hello, nice to meet you

I´m Jacqueline and I grew up surrounded by the Italian Alps. I have a strong passion for writing about science in all its shapes. With 4+ years of experience in preclinical R&D and Oncology, I now combine scientific knowledge with my passion for writing and communication to build informative stories and content for different targets. 

After completing a Master's degree in Pharmacy, I attended a Postgraduate program in Drug design and development, which enabled me to work in preclinical R&D in several industrial environments. I then earned a PhD in Oncology and most recently acquired hands-on experience in the Regulatory field.

My broad background knowledge enables me to tackle your projects from various angles and complete tasks according to your requirements competently.

I strongly value continuous learning and professional growth. I regularly attend workshops and courses to learn new content and strengthen my skills in Medical writing.
I am a fast learner and a precise and organised work partner who enjoys learning always new things and meeting people from different backgrounds.

​Something I realized during these years: although becoming the smartest guy in the room is the ultimate goal, I’m very satisfied when I’m not.

My Scientific Qualifications

4+ years of experience in preclinical R&D, Oncology and Regulatory affairs in industrial environments 

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PhD in Cancer Biology funded by the Marie Skłodowska-Curie grant

Charles River Laboratories and Albert-Ludwigs-Universität Freiburg, Germany

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Postgraduate Professional Program in Drug design and Development

Università di Pavia, Italy

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MSc in Pharmacy

Università degli studi di Torino, Italy

Other qualifications and certificates

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"Clinical Study Reports - Mastering the Essential Skills"

EMWA

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"Beginner’s Guide to Key Clinical Documents in the EU Drug Development Process"

EMWA

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​“Sharpen Up Your Writing Skills”

EMWA

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"Communicating Research: Paper Writing And Short Presentation" ​EMBO solution GmbH

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"Good Clinical Practice"

National Drug Abuse Treatment Clinical Trials Network

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"Regulatory Medical Writing Basics"

Udemy

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“Design and Interpretation of Clinical Trials”

The Johns Hopkins University

Work experiences

I feel satisfied to have had the opportunity to work in various environments over the years. Each experience has been invaluable in shaping my professional and personal growth. I’ve learned to adapt, collaborate with diverse teams, and develop a deeper understanding of my field. This also increased my ability to work on different tasks simultaneously, be an active listener, and develop a proactive mindset.

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Employment History​

Freelance Medical Writer - April 2024 - Present

QM Associate – Regulatory affairs at Dr. Langer Medical, Waldkirch (DE) - December 2023 — May 2024

Marie SkÅ‚odowska-Curie PhD fellow at Charles River Laboratories, Freiburg im Breisgau (DE) - February 2020 — January 2024

Visiting PhD researcher at Medical University of Vienna, Vienna (AT) - October 2021 — December 2021

Associate researcher at RBM Merck S.p.A., Colleretto Giacosa (Turin), (IT) - July 2019 — February 2020

Research Intern at APHAD S.r.l and Mario Negri Institute of research, Milan area, (IT) - September 2018 — March 2019

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Contact

I'm always looking for new and exciting opportunities. Let's connect.

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