Editor's Salary at The Press Democrat BETA

Medical Writer Location: San Rafael, CA. (Hybrid) 7 month assignment (Potential to extend) Pay Rate: $52/hr. On behalf of our client a pharmaceutical company specializing in the development of therapeutics for patients dealing with rare genetic life threatening diseases. The Contract Medical Writer applies advanced expertise in document preparation and project management to support the development, drafting, review, and finalization of clinical study documents. These documents are critical for regulatory submissions and publications, ensuring the accurate reporting of clinical study results. Main Responsibilities: Draft and edit documents for regulatory submissions, including Common Technical Documents (CTDs) and Responses to Questions (RtQs). Develop and refine documents used in clinical studies, such as protocols, protocol amendments, and informed consent forms. Prepare documents for reporting aggregate safety and efficacy data, including investigator brochures and periodic safety re

The Contract Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications. Responsibilities: Drafts and edits documents used for submissions including CTDs and RtQs Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, and informed consent forms Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PSURs, DSURs, etc.) Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes Adheres to departmental procedures and

Job Title: Medical Writer Location: San Rafael, CA 94901 (Hybrid) Duration: 6 months assignment Hourly pay range: $55-$57/hr Responsibilities: Drafts and edits documents used for submissions including CTDs and RtQs. Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, and informed consent forms. Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PSURs, DSURs, etc.). Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes. Adheres to departmental procedures and practices and technical and industry standards during all aspects of work. Works effectively with cross-functional groups within client. Other tasks as assigned. Skills: Fulfils one of

Job Description RH at its core is about taste, and we believe the idea of scaling taste is large and far reaching. The RH brand attracts the best designers, artisans, manufacturers and talent in our industry, scaling and rendering their work more valuable across our integrated platform, enabling us to curate the most compelling collection of luxury home furnishings in the world. We are moving the brand beyond curating and selling products to conceptualizing and selling spaces by building an ecosystem of products, places, services and spaces that elevates and establishes the RH brand as a global thought leader, taste and place maker. At RH we believe deeply that the "right" people are our greatest asset. We value people with high energy, who possess the ability to energize others. People who are smart, creative and have a point of view. People who see the answer in every problem, versus those who see the problem in every answer. People who are driven, determined and won't take "no" for

The Contract Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications. RESPONSIBILITIES Drafts and edits documents used for submissions including CTDs and RtQs Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, and informed consent forms Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PSURs, DSURs, etc.) Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes Adheres to departmental procedures and

The Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications. RESPONSIBILITIES Drafts and edits documents used for submissions including CTDs and RtQs Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, and informed consent forms Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PSURs, DSURs, etc.) Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes Adheres to departmental procedures and practices

Position: Medical Writer, Req#: 35551628 Location: San Rafael, CA (Remote or hybrid depending on the location of the candidate (1-2 days in office to align with company policy)). Duration: 6+ Months Contract Job Description: The Contract Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications. Education and Experience: Bachelor’s or higher degree; scientific focus desirable. Evidence of medical writing career development desirable, eg, American or European Medical Writers Association certificate, Editor in Life Sciences certificate, or relevant training through Drug Information Association. At least 5 years of experience required Medical writer in the pharmaceutical industry Medical or scientific writing experience as a primary job responsibilit

Job Description About the Team Digital Web Creative is a dynamic team of talented, digital marketing designers and digital production coordinators. We work closely with our editorial team members to make our websites, emails and digital assets come alive with the Pottery Barn Kids' brand voice. We also collaborate closely with our cross-functional partners in eCom, Development, Brand Marketing and Merchandising to name a few! We are all about sharing creative ideas and supporting each other to not only do our best work, but also to build a strong sense of family and community. Come join our team! About the Role Responsible for editing video content for the Pottery Barn Kids and Pottery Barn Teen digital platforms and channels. This is an onsite role based in our Richmond, CA photo studio. You're excited about this opportunity because you will... Create engaging vertical videos for usage across our social platforms like Instagram and TikTok Have a digital first and socially lead approac