Senior Regulatory Writer

Job Title: Senior Medical WriterAt Celegence, we are seeking a highly skilled Senior Medical Writer to join our team. As a Senior Medical Writer, you will be responsible for developing high-quality regulatory documents for medical devices across various therapeutic areas.Key Responsibilities:Develop and deliver regulatory documents compliant with MEDDEV...

Job Title: Senior Medical Writer/Medical WriterVCLS is a leading provider of medical writing services in the pharmaceutical industry. We are seeking a highly skilled Senior Medical Writer/Medical Writer to join our team.Key Responsibilities:Author high-quality medical documents for client projects, including study protocols, investigator brochures, and...

Job SummaryClinChoice is seeking a skilled Senior Medical Writer to join our team. The ideal candidate will have experience in medical writing for regulatory documents, such as clinical study reports, protocols, and CTD sections.Key Responsibilities:Research and create high-quality clinical documents for regulatory submissions.Collaborate with project teams...

  Job Title: Regulatory Scientific Writer Job Summary:We are seeking a highly skilled Regulatory Scientific Writer to join our Medical Affairs team at Lilly. As a Regulatory Scientific Writer, you will be responsible for developing high-quality, regulatory-grade documents that support the development and approval of pharmaceutical...

We're seeking a skilled Regulatory Writer to join our team at Lilly. As a key member of our Scientific Communications team, you'll play a critical role in developing high-quality regulatory documents that support our clinical development and product registration efforts.Key Responsibilities:Develop and maintain a deep understanding of regulatory guidelines...

Senior Medical Writer/Medical WriterVCLS is seeking a highly skilled Senior Medical Writer/Medical Writer to author high-quality medical documents for various client projects. The primary goal is to deliver accurate and timely documents that meet regulatory standards and guidelines.Key Responsibilities:Act as the lead medical writer on client programs,...

Job SummaryThe Principal Medical Writer - Clinical Regulatory Documents is a key member of our team at ScaleneWorks, responsible for creating high-quality, compliant clinical regulatory documents. This role requires a strong understanding of clinical trial designs, data interpretation, and regulatory requirements.Key Responsibilities Develop and maintain a...

Job SummaryThe Principal Medical Writer is a highly skilled and experienced professional responsible for creating high-quality clinical regulatory documents. This role requires a deep understanding of clinical trial designs, statistical analysis, and regulatory requirements. The ideal candidate will have a strong background in clinical regulatory writing,...

ClinChoice is seeking a highly skilled Regulatory Document Medical Writer to join our team.About the Role:The Medical Writer will be responsible for researching, creating, editing, and coordinating the production of clinical and regulatory submission documents, including clinical study reports, protocols, CTD sections, IB, and safety update...

Clinical and Regulatory Submissions Medical WriterAt ClinChoice, we are seeking a highly skilled Medical Writer to join our team.About the RoleThe Medical Writer will research, create, edit, and coordinate the production of clinical and regulatory submission documents, including clinical study reports, protocols, CTD sections, IB, and safety update...

ClinChoice Medical Writing RoleJob SummaryClinChoice is seeking a highly skilled Regulatory Medical Writer to support our clinical research initiatives. The ideal candidate will have strong clinical/scientific writing skills and experience in medical writing for regulatory submissions.ResponsibilitiesResearch, create, edit, and coordinate the production of...

Parexel Career OpportunitySenior Medical WriterThe Senior Medical Writer is responsible for creating, editing, and managing all documents associated with clinical research. This role may act as the project lead writer/submission coordinator and primary client contact, overseeing contributions from multiple writers working on related documents. The Senior...

Medical Writing Expertise at ParexelThe Senior Medical Writer will be responsible for researching, creating, and editing all documents associated with clinical research. This role may involve operating as the project lead writer/submission coordinator and primary client contact to manage contributions of multiple writers working on related documents.Key...

Parexel seeks a highly skilled Principal Medical Writer to lead the creation and editing of clinical research documents.The successful candidate will have 10+ years of experience in regulatory medical writing and be proficient in authoring protocols, clinical study reports, and other documentation.Main Responsibilities:Research and create high-quality...

About the RoleThe Senior Medical Writer will be responsible for researching, creating, and editing all documents associated with clinical research. This includes protocols, clinical study reports, investigator's brochures, informed consent forms, and summary documents. The ideal candidate will have experience in regulatory medical writing and be able to...

Parexel: A Leading Provider of Medical Writing ServicesSenior Medical Writer RoleThe Senior Medical Writer will be responsible for creating and editing all documents associated with clinical research. As part of the Medical Writing Services team, this individual will operate as the project lead writer/submission coordinator and primary client contact to...

• At ScaleneWorks, we are seeking a Senior Clinical Writer to drive the creation and review of high-quality clinical documents, including protocols, clinical study reports, and regulatory submission documents. • The ideal candidate will have a strong understanding of clinical trial designs, statistical analysis, and regulatory requirements. • Key...

Delivering High-Quality Clinical Research DocumentsThe Senior Medical Writer will be responsible for researching, creating, and editing all documents associated with clinical research. This includes protocols, clinical study reports, investigator's brochures, informed consent forms, and summary documents. The ideal candidate will have experience in...

Senior Medical Writer/Medical WriterVCLS is seeking a highly skilled Senior Medical Writer/Medical Writer to contribute to the development of high-quality medical documents for various client projects.Key Responsibilities:Act as the lead medical writer on client programs, ensuring the highest quality of deliverables.Review draft and final documents prepared...

Job DescriptionWe are seeking a highly skilled Senior Technical Writer to join our team at Actian Corporation. As a Senior Technical Writer, you will be responsible for developing, writing, and maintaining technical documentation for our database management systems, including Actian Ingres, Vector, and Actian X.Key Responsibilities:Gather information from...