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Senior Medical Writer

Pubblicato il 06-09-2026 - Parexel in Vercelli

About Parexel Parexel is a leading global clinical development partner delivering insights driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient focused clinical trials that broaden access and make research a care option for anyone, anywhere.
About Parexel Parexel is a leading global clinical development partner delivering insights driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient focused clinical trials that broaden access and make research a care option for anyone, anywhere. We work with focus, agility, and shared purpose, moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research.



We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart.
About The Role We are seeking an experienced Medical Writer to join a key functional service provider program supporting one of our key sponsors. As a Medical Writer, you will act as an integrated resource within the team, delivering Medical Writing Services for the creation of clinical documents including CTRs, CTPs and amendments, IBs and updates, biomarker reports, and submission documents. Working in a dedicated sponsor aligned environment, you will contribute to high-quality clinical development programs through close collaboration, scientific communication, and proactive project engagement.
Key Responsibilities
- Document management within the EDMS.
- Review and approval of Statistical Analysis Plans in the EDMS.
- Management of timelines and ongoing schedule updates.
- Preparation for and attendance at trial team and submi

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