You are a talented professional with a sound scientific academic background. You will be challenged with numerous and diverse projects that include conducting researches, writing and editing clinical reports, analysing and summarizing statistical data from clinical studies, writing clinical study protocols and sections of regulatory submission documents, writing paper for submission to high level scientific journals.

Take your time in reading this job post and if you see an opportunity for your career do not hesitate to get in touch.

A day in the job

Your daily activity will be very diverse and will include the following activities:

  • Analysing clinical evidence of all kinds (public, proprietary, published or unpublished, etc.) from all sources (journals, internal documents, regulatory submissions, etc. ) in order to assist customers, colleagues and management.
  • Understanding levels of evidence required to achieve regulatory, marketing, and regulatory goals.
  • Supporting publication of high-quality articles featuring results of clinical studies and other forms of clinical evidence in medical journals.
  • Creating and maintaining Clinical Evaluation Reports (CERs) and others scientific documentation in compliance with the regulations for product clearance/certification in Europe and other selected geographies. Assessing on an ongoing basis the quality, scientific validity, and audit-readiness of customers’ CERs.
  • Conducting comprehensive literature searches to support research, clinical evidence, product development, risk analysis, regulatory submissions. Writing ad hoc reports based on these literature searches.
  • Compiling, analysing and summarizing data applying simple statistics and using statistical software packages such as R, Origin, G*Power, etc.
  • Conceive and design tables, charts, figures, and other visual display elements for presenting scientific and clinical data.
  • Supporting preparation of abstracts and/or scientific exhibits, posters and presentations.
  • Remaining current with UE regulatory framework and with medical writing hot topics, including ethics and best practices.
  • Assisting other members of the team in effective visual and written scientific communication
  • Other non-routine duties as required by the business.

What we expect

The candidate must ensure services are rendered to customers in a timely manner and according to the high quality standard expected by the company. Reporting to a senior manager, the candidate will show a clear ability to work both autonomously and in close collaboration with the corresponding functions in the other areas in which the company operates: regulatory affairs, quality management systems, scientific communication & marketing.

What we give in return

In return the candidate will be exposed to a buoyant, stimulating professional environment, will be rewarded with a competitive salary, and other benefits. Clariscience supports continuous educations and as such encourages employees to improve existing skills and acquire new ones through a personalised learning path including both internal and external courses.


The candidate holds a degree in a scientific discipline, such as Biological Sciences, Pharmacy, Medicine and Biotechnology. A PhD in one of these disciplines is welcome but not mandatory.

We expect only people with 2+ years of medical writing experience (gained within the academic or industry sector) to apply for this position.

The candidate speaks fluently and writes in Italian and English. The knowledge of another European language (French, German, Spanish) is welcome but not necessary.

To qualify, applicants must be legally authorized to work in the European Union.

This offers refers to a full time position. Workplace is located in Padua city centre.


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