Clinical Medical Writer

Spectraforce Technologies
United States, Illinois, Lake Forest
Mar 22, 2025
Title: Clinical Medical Writer Duration: 9 months Location: Lake Forest, IL 60045 One candidate will be recruited to work in Lake Forest, Chicago, and two candidates will be recruited to work in Europe. The US candidate is sought to fill one of the following positions: 1) Medical Writing: Additional clinical resource is required to support the ongoing IVDR remediation program, to ensure IVDR compliance in a timely manner. The Contingent Worker will support data generation through literature searches and data collation and dissemination. This will be in support of on-market products going through IVDR remediation. It is expected that the Contingent Worker will generate the initial clinical performance report, which then will be updated on an annual basis. The candidate will be skilled in medical writing, developing literature search protocols, and interpreting and selecting relevant scientific literature. Proficiency in Microsoft Word, including creating, tracking changes, and formatting documents to a final signable state, is essential. 2) Medical Writing and Study Execution: Additional clinical resource is required to support the ongoing IVDR remediation program, to ensure IVDR compliance in a timely manner. The Clinical Project Manager will support data generation through literature searches and data collation and dissemination. This will be in support of on-market products going through IVDR remediation. It is expected that the Clinical Project Manager will generate the initial clinical performance report, which then will be updated on an annual basis. The Clinical Project Manager will be skilled in medical writing, developing literature search protocols, and interpreting and selecting relevant scientific literature. Proficiency in Microsoft Word, including creating, tracking changes, and formatting documents to a final signable state, is essential. Furthermore, the Clinical Project Manager will also be skilled in clinical study start-up and execution. The Clinical Project Manager will provide support for IVDR study execution, as needed. The activities of this role will be in support of on-market products going through IVDR remediation as well as for new product requiring studies to comply with IVDR requirements.