- System One (Park Ridge, NJ)
- Title: Sr Regulatory Writer - R&D Location: Park Ridge, NJ area Schedule: M-F Full Time Type: Direct Hire Responsibilities: Our client is seeking Regulatory writing ... (EPA, DIN) and general household products areas. The Senior Writer will lead and drive the technical (CMC) writing...Prepares and/or assists in the coordination and preparation of scientific documents under minimal supervision to meet or exceed… more
- OPEN Health (NJ)
- Medical Writer , Medical Communications Job Summary Our Medical Writers provide research and writing support to assigned brand teams and new business efforts. They ... support and/or repurposing technically high-level projects. Projects include abstracts, scientific posters, oral presentations, outlines, primary and review articles… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Senior Medical Writer (SMW) works with team members and independently to write the content of clinical documents that may include CSRs, protocols, ICFs, ... Plans, TFLs) to help ensure appropriate content for inclusion. **As a Senior Medical Writer , a typical day may include:** + Works with the clinical team, to write… more
- RELX INC (Trenton, NJ)
- …RFPs/RFQs/RFIs and other proposal documents. About the Role: The Senior Proposal Writer responses to state and local government (SLG) agencies' Requests for ... is to benefit society by developing products that help researchers advance scientific knowledge; doctors and nurses improve the lives of patients; lawyers promote… more
- Actalent (Cranbury, NJ)
- Job Title: Technical WriterJob Description The role of Technical Writer involves developing, reviewing, and maintaining technical documents related to Analytical ... PowerPoint. + Strong attention to detail and ability to translate complex scientific information into clear documentation. + Ability to work independently and… more
- Vitalief (Newark, NJ)
- …result, we are seeking a talented and enthusiastic Senior level Senior Pre-Award Grants Writer for a variety of short-term (ad hoc, meaning could be either part-time ... Vitalief: + You can actively contribute to our clients' mission of advancing scientific discoveries that have the potential to change patients' lives for the better.… more
- Publicis Groupe (Morristown, NJ)
- …management and attention to detail + Has the ability to digest scientific data/information and interpret its application for formulary decision-makers + Ensures ... deliverables are properly prepared for submission to medical/legal/regulatory review, including referencing, annotating, and adherence to regulatory requirements + Can effectively present and sell their work, both internally and to clients + Maintains… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve ... and commercial product lifecycle management and contributes strategic, expert input into scientific and regulatory content that is used for a variety of purposes,… more
- EBSCO Information Services (Trenton, NJ)
- …and regular review of content collection + Support culture of teamwork and writer development through effective editing and feedback + Maintain quality of content ... setting + > 2 years of writing experience related to medical or scientific content + Demonstrated understanding/use of principles of evidence-based practice and use… more