Medical Writer - Des Plaines

This role focuses on authoring and editing technical documents to support domestic and international regulatory submissions. · ...

Author technical documents with a high level of detail and precision to support domestic and international regulatory submissions. · ...

This is a Medical Writer role that will be responsible for leading and executing all medical writing activities supporting Xeris' clinical programs.The individual will have a strong scientific background, exceptional writing skills, and the ability to translate complex clinical a ...

Dice is the leading career destination for tech experts at every stage of their careers. Our client, Source Infotech, is seeking the following. · Author technical documents with a high level of detail and precision to support domestic and international regulatory submissions. · ...

Reporting directly to the Vice President of Clinical Development, the Medical Writer will be responsible for leading and executing all medical writing activities supporting Xeris' clinical programs. · ...

Reporting directly to the Vice President of Clinical Development, the Medical Writer will be responsible for leading and executing all medical writing activities supporting Xeris' clinical programs. · ...

Write and edit high-quality medically relevant AMCP dossiers for assigned therapeutics areas or assets to fulfill medical scientific and health economic objectives. · ...

Write and edit high-quality medically relevant AMCP dossiers for assigned therapeutics areas or assets to fulfill medical scientific and health economic objectives. · ...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. · Creates/updates technical documents for medium-risk blood screening product international regulatory submissions (e.g., IVDR Class B). · ...

The AMCP Medical Writer specializes in developing, editing and managing evidence-based dossiers following the Academy of Managed Care Pharmacy (AMCP) format. · Write and edit high-quality, medically relevant AMCP dossiers for assigned therapeutics areas or assets to fulfill medic ...

Net2Source is hiring a Senior Medical Writer for one of our clients. The role involves writing and execution of clinical drug trial registrations on trial registries per regulatory and SOP requirements. · Bachelor's degree in health or biological science field. · Must have 2+ yea ...

The job requires a Medical Writer III with 5+ years of experience in medical or scientific writing to write and edit high-quality medically relevant AMCP dossiers for assigned therapeutics areas or assets. · Developing editing and managing the production of AMCP Dossiers and scie ...

+ Write and edit high-quality medically relevant AMCP dossiers for assigned therapeutics areas or assets to fulfill medical scientific health economic objectives · + Ensure successful preparation of high quality submission-ready documents effective implementation of writing proce ...

The Value & Access Principal AMCP Medical Writer is responsible for writing and editing high-quality, medically accurate AMCP dossiers and related payer-focused materials across assigned therapeutic areas or assets. · PharmD, PhD, or equivalent advanced scientific degree · 3-5 ye ...

This is a medical writing position for AMCP dossiers. · Developing managing production of AMCP Dossiers and scientific presentations · ...

+This role is a premier opportunity to write and edit high-quality medically relevant documents for assigned therapeutic areas. You will ensure the successful preparation of submission-ready documents and the effective implementation of the writing process. · ...

Responsibilities include researching and analyzing scientific information to answer escalated MI inquiries and creating scientific response documents ensuring that responses are medically and scientifically accurate timely fair balanced meet customers needs. · ...

The Senior Strategic Medical Writer is responsible for leading and writing clinical and regulatory documents for drug and/or device development in support of company objectives. · Prepares clinical and regulatory documents needed for the development of AbbVie drugs and/or devices ...

The Senior Strategic Medical Writer is responsible for leading and writing clinical and regulatory documents for drug and/or device development in support of company objectives. · Prepares clinical and regulatory documents needed for the development of AbbVie drugs and/or devices ...

· ,,,Maintains awareness of current industry practices that pertain to Corporate Policies and Procedures. · Must continually train/be compliant with all current industry and company requirements · , ...