Writer Salary at Learn It! BETA

Job Description Job Description Service Writer Duties and Responsibilities Service Writers answer questions from customers and service providers. They use their expert knowledge to understand the client’s problems and explain their needs to staff for satisfactory service delivery. Service Writers also schedule appointments, process orders, monitor delivery and handle customer complaints. Their duties include working with computers and building and maintaining relationships. Here are examples of Service Writer duties: Interact with customers, listen to their questions and concerns and provide timely responses. Educate clients about the company’s products, services and offers. Schedule appointments, take orders, monitor service progress, calculate charges and process payments. Review customer accounts and report changes to internal staff. Manage complaints, returns and resolve customer grievances. Record customer details and transactions. Serve as a customer relationship manager. Serve a

Job Description Job Description An AMLaw 100 firm is currently seeking skilled applicants with strong writing skills to join their practice as a Legal Writer. The ideal candidate will have outstanding writing skills and prior law firm or legal services experience. This is a contract role lasting through 01/20/2025 with an immediate hiring need. 100% remote - West Coast Hours Contract - ASAP start date through at least 01/20/2025 Pay starting at $30/hour (OT paid at time and a half) Legal Writing experience required Duties Responsibilities will be to write and edit immigration petition support letters, translate technical and legal language, develop 20-40 page legal case documents, update and maintain case related documents, and more. Individuals in this position will work frequently with National Interest Waiver (NIW) and EB1 work. Duties will include drafting petitions, NIW and EB1 documents, and other legal documents as assigned by attorneys and senior staff. Research, analyze, and w

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

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

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

Overview: Audacys KCBS All News Radio, The Bay Areas number one news station, is always looking for an intrepid and tech-savvy journalist with a positive attitude and impressive work ethic to join an elite news team in the capacity of part-time news writer. KCBS is a 24/7 live and local news station. The part-time news writer schedule varies and is based in part on station needs plus planned and breaking news events. Potential shifts can include 5a-12p and/or 11a-7p. Responsibilities: What Youll Do: Create (from scratch) and update existing broadcast and wire copy to create compelling, interesting, informative and accurate broadcast-style scripts for news anchors to deliver via radio broadcast and digital stream Write compelling teases (that dont give the story away!) Incorporate sound bites, music, sound effects and other elements to enhance your news copy Edit and produce newscasts (including but not limited to selecting, editing and/or writing news content) Edit audio for broadcast