This listing was posted on The Resumator.
Medical Writer (Assay Development)
Location:
Wilrijk
Description:
Medical Writer (Assay Development) 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. 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! The information collected to review your application will be processed by the human resources services of CellCarta Biosciences Inc. and its affiliates (collectively, “CellCarta”). The legal basis for this processing is the legitimate interest of CellCarta to evaluate the suitability of candidates for the roles available at CellCarta. CellCarta will only process that information which is necessary to evaluate your application. This information includes identifying information such as your name, address, email address and phone number, as well as information about your education and professional experience, including previous positions and your CV. Such information is required for us to complete your applicant file, assess your suitability for the role and comply with applicable laws. CellCarta may obtain personal information from other sources, such as during reference, background, or employment checks, with your permission, and from third party sources such as recruitment and assessment sites or professional social media sites, in each case only if such information is relevant to reviewing your application. Your personal information will be retained only for so long as reasonably necessary and in accordance with applicable laws. This information will be processed confidentially and only accessed by those who have a need for the recruitment process. Please note that the information comprising your applicant file may be processed in a country that is not where you are located (for example, you might be in the European Economic Area or Québec, Canada, whereas your applicant file may be reviewed by CellCarta in the United States). If you are offered and accept employment with CellCarta Biosciences Inc. or one of its affiliates, the information collected will become part of your employment record. If you do not want us to retain your information, or want us to update it, please contact XXXX@cellcarta.com . Powered by JazzHR
Company:
Cellcarta
Posted:
April 6 on The Resumator
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