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Journalism

106 jobs found

Nov 23, 2023  
REGIONAL DIGITAL SALES MANAGER (REMOTE/USA) - GDM (Gray Media Group)
About Gray Television: Gray Television is a leading media company that owns and operates high-quality stations in 113 television markets that collectively reach 36 percent of US television households.  We constantly strive for excellence. Through upgrading to the latest technology and seeking new ways to stay on top in our markets, we focus on training and development of the best and brightest employees in the business. About Gray Digital Media: It’s no secret that our industry is changing rapidly. The Gray Digital Media Sales team is tasked with keeping our station’s sales staff in the know and on the street selling. This position is fast-paced, challenging, strategic, and rewarding. We are looking for people who are self-starters and are interested in leading and developing great salespeople. You must be comfortable with handling big accounts, strategic decisions, and sometimes campaign issues, from start to finish. You must be confident with change and handle...
Gray Television Charlotte, NC, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing Portland, OR, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing CA, United States, CA, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing Nashville, TN, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing Orlando, FL, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing St. Louis, MO, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing San Diego, CA, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing Raleigh, NC, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing Cleveland, OH, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing Washington, DC, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing Denver, CO, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing Minneapolis, MN, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing Salt Lake City, UT, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing San Jose, CA, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing Irvine, CA, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing Las Vegas, NV, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing Charlotte, NC, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing San Antonio, TX, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing Kansas City, MO, USA
Nov 23, 2023  
Medical Writer II - REMOTE
Proclinical is seeking a Medical Writer II for a rare disease biotech company headquartered in San Francisco. This position can be fully remote. The Medical Writer II will focus on documentation preparation and document project management to assist in the development, review, and finalization of documents including protocols, protocol amendments, informed consent forms, and clinical study reports. Must be eligible to work in the US. Job Responsibilities: Draft and edit documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports Draft and edit documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator's brochures and periodic safety reports (PSURs, DSURs, etc.) Provide peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials Skills and...
Proclinical Staffing Phoenix, AZ, USA