Medical Writer (Assay Development)

CellCarta

Antwerp, Belgium

Are you looking for an exciting new opportunity? CellCarta, a renowned Contract Research Organization, is actively seeking a highly skilled and motivated Medical Writer to join our dynamic team. In this role, you will play a pivotal role in building out our company's assay development strategy, ensuring compliance with industry standards, and driving continuous improvement. Join us and collaborate with a team of dedicated professionals who are passionate about advancing patient therapy and making a real difference in the world. Apply today!

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;
Ability to rapidly learn and apply knowledge in previously unfamiliar areas;
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.

Apply Now

Don't forget to mention EuroPharmaJobs when applying.

Share this Job