Medical Writer

**Medical Writer (Assay Development)**

**Summary**

Reporting to the Scientific Lead of Assay Development - Histopathology, the Medical Writer writer is responsible for completing different types of documents such as scientific plans and reports, needed for the development and validation of assays to be used for clinical sample testing. Those documents will need to comply with quality standards for internal documentation and for external stakeholders like healthcare professionals and/or authorities.

**Responsibilities**
- Adherence to company policy on patient and client confidentiality.
- Manage and plan activities to deliver in a timely manner and communicate proactively and effectively about the progress of your work with the different involved participants.
- Efficiently complete literature search and summarize these data.
- Formalize and standardize all scientific content delivered primarily by the assay development team.
- Proofread and edit documentation so that the content is direct, easy-to-read, and compelling, while maintaining technical accuracy.
- Convert raw data and data reports into an easy-to-understand and streamlined narrative.
- Provide support in defining and refining the workflow for report writing and associated tasks.
- To participate in the elaboration and continued improvement of report templates.
- Identify gaps and inefficiencies in the process and propose solutions.

**Education**
- Master in Life Sciences (preferably Biology, Biomedical Sciences, Bioengineering, Pharmaceutical sciences, Biochemistry) or equivalent through experience.

**Main Requirements**
- Previous experience in medical/scientific writing is preferred.
- Basic knowledge of histology/histopathology and/or microscopy is an asset.
- Strong computer skills and significant experience with Microsoft Excel, PowerPoint and Word are required.
- Excellent command of the English language and outstanding writing and communication skills.
- Exceptional attention to detail.
- You are highly organized, and able to manage and prioritize multiple projects.
- Methodically, meticulously and demonstrate quality of work including accuracy.
- Timeliness, professionalism, conciseness, and thoroughness.
- Must be able to understand complex scientific information.
- You are social, diplomatic, a team player and a strong communicator.

**Working Conditions**
- Hybrid role: 2-3 days onsite

**What can we offer**
- A dynamic and rapidly changing global environment allowing personal growth
- Training and personal development in a variety of (technical or people related) areas
- True career opportunities as the company grows fast. You can build on the road
- A healthy work life balance with on-site and remote working
- A company that is fit for the future
- A competitive salary and benefits
- A great team you can work with

**About CellCarta**

CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The company operates globally with over 1000 employees in its 11 facilities located in Canada, USA, Belgium, Australia, and China.

**Join us as we make an impact on the future of patient therapy**

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