Managing Editor Salary at I-Connect007 BETA

Video editing is the final frontier of software tools moving to the cloud. We're making the next generation of modern creators tools to enable everyone to share their story online. Join us at Kapwing on our mission to make content creation fast, accessible, and collaborative. Everyone is a creator. The problem, however, is that today's tools get in the way of expressing our creativity fully. Especially when it comes to video, the gap between an idea and a video is wide enough that it's hard to even start. Our mission at Kapwing is to make content creation easier and more accessible. Our main product, Kapwing Studio, is an online video editor that is both powerful and easy to use. Millions of creators every month choose Kapwing to tell their story and bring their ideas to life. Our vision is to build a modern video editing platform that serves as the go-to tool for anyone creating video for Youtube, social media, or work. Kapwing turns video editing, traditionally a heavyweight, time co

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

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

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 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

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

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 San Francisco Standard is seeking a dynamic and enterprising editor to help oversee political coverage in our fast-growing, fast-moving newsroom. In this role, you will assist our politics editor in managing a small team of reporters focused on San Francisco government and elections. The ideal candidate has experience covering politics, as an editor or senior reporter, in the Bay Area or at the state level. You should be familiar with the most important local elected officials, candidates, organizations and donors, and be well-versed in the major issues facing San Francisco, including crime, corruption, homelessness, the housing shortage and the decline of downtown as a business district. Can you find in these topics fresh story ideas and angles that grab the attention of the 90% of San Franciscans who don't follow politics day-to-day? That's our mission. Your duties will include assigning and editing breaking news, features and investigations while helping to shape strategy and pl