Scientific Writer

Scientific Writer to Galderma in Uppsala

Do you have a background within Life sciences and experience from scientific writing and literature surveillance of scientific databases? Are you interested in taking part in a small team of professionals focusing on post market clinical evaluation and monitoring? Then you should continue to read as we are now looking for a Scientific Writer for Galderma to be based in Uppsala.

The Clinical Evaluation and Monitoring team within Medical Affairs at Galderma generates data in the postmarket clinical follow up phase to fulfil the requirements for market authorization of approved Galderma aesthetic products in accordance with regulatory requirements.

Responsibilities

As a Scientific Writer within this team you will manage postmarket clinical follow up, including planning, analyzing and reporting, and contribute in overall postmarket surveillance processes. You will also contribute in compilation and periodic updates of clinical evaluation plans and reports for each product group. Other work tasks may include:

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Contributing, reviewing and approving documentation for regulatory purposes e.g. labeling material, design dossiers, annual reports, questions from Health Authorities worldwide
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Providing scientific expertise including generating clinical supportive data based on clinical literature and/or clinical studies
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Supporting cross functions in expertise review, for example risk management

Requirements

We are looking for an organized, motivated and detail-oriented person with a university degree in Biology, Pharmacy, or Medicine; preferably MSc or MD, followed by a few years work experience. If you have a PhD within life sciences/medical sciences it is considered meriting for this role, as is experience in compilation of documents for regulatory submissions in EU and worldwide, as well as knowledge in international medical device regulation including EU Medical Device regulation 2017/745. You have:

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Thorough experience in compilation, analysis and dissemination of scientific information (> 3 years)
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Thorough experience in literature surveillance of scientific databases
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Knowledge in Good Clinical Practice.
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Proven verbal and written communication skills and ability to work cross-functionally
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Good knowledge in MS Office applications

You will thrive in this role if you enjoy going through medical literature and scientific databases, and have the patience to read, understand, and communicate clearly (in writing and orally) with others what you have discovered. As a person, you must be used to working individually while also being part of the team and being there to answer questions and present data to a broad range of internal and external stakeholders.

Does this sound interesting? Please apply with CV and cover letter via this page, alternatively via the link Apply now, no later than November 21st. Selection and interviews might be done continuously so do not wait with your application. If you have any questions, please contact Birgitta Almegård,