- Merck & Co. (Rahway, NJ)
- …and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for developing ... regulatory requirements, and health literacy principles.With minimal oversight, the Senior Informed Consent Medical Writer :Demonstrates independence… more
- Merck & Co. (Rahway, NJ)
- …and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for developing ... with internal policy, regulatory requirements, and health literacy principles.With oversight, the Informed Consent Medical Writer :Demonstrates growing… more
- Merck (Carson City, NV)
- …and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for developing ... requirements, and health literacy principles. **With minimal oversight, the Senior Informed Consent Medical Writer :** + Demonstrates independence in… more
- Merck (Carson City, NV)
- …and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for developing ... policy, regulatory requirements, and health literacy principles. With oversight, the Informed Consent Medical Writer : + Demonstrates growing independence… more
- University of Miami (Miami, FL)
- …including but not limited to clinical trial protocols and informed consent documents (ICFs). The Scientific Writer is integrally involved with managing ... has an exciting opportunity for a Full Time Scientific Writer ( Medical Writer ) to work...research including, but not limited to study protocols and informed consent forms. 2. Collaborate with PI,… more
- System One (New Haven, CT)
- Job Title: Medical Writer (part time) Location: Northeast (EST) candidates preferred Hours: 30 hours/month (7-8 hours/week) Type: Contract (C2C or W2) Job ... Purpose The Translational Research Medical Writer plays a key role in...finalization of clinical research documents, supporting the creation of Informed Consent Forms (ICFs), clinical protocols, and… more
- Astrix Technology (Chicago, IL)
- ** Medical Writer ** Medical ...Investigator's Brochures (IBs) + Clinical Study Reports (CSRs) + Informed Consent Forms (ICFs) + Clinical sections ... a diverse range of clients across various industries. We're seeking talented Clinical Medical Writers to join us! Our partners range from emerging biotech firms to… more
