Regulatory Writer

  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...

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...

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...

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 Description for Senior Medical Writer Key Responsibilities:Develop and deliver high-quality regulatory documents for Medical Devices across therapeutic areasEngage with internal stakeholders and client business teams for customized solutionsManage project timelines and train junior team membersRequirements:Bachelor's/Master's degree in Life Sciences with...

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...

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 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...

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...

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,...

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,...

About this roleWe are looking for a talented Regulatory Writer to join our team at Lilly. As a key member of our scientific communications team, you will play a critical role in creating high-quality, regulatory-grade documents that support clinical development and product registration.Key responsibilitiesDevelop and write regulatory documents, including...

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...

Clinical Documentation SpecialistAt ClinChoice, we are seeking a highly skilled Clinical Documentation Specialist to join our team. As a key member of our medical writing team, you will be responsible for creating, editing, and coordinating the production of clinical and regulatory submission documents.Key Responsibilities:Research and create clinical...

We're seeking a highly skilled Regulatory Writer to join our team at Lilly, contributing to the development of documents for regulatory audiences.Key Responsibilities:Develop and execute content strategies for writing projects, collecting and evaluating data from various sources.Plan, write, edit, review, and coordinate regulatory documents supporting...

Parexel is seeking a highly skilled Regulatory Medical Writing Lead to join our team.The successful candidate will have experience in creating and editing documents associated with clinical research, including protocols, clinical study reports, and investigator's brochures.Key responsibilities include:Researching and authoring high-quality...

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...

Job Title: Principal Medical WriterJob Summary: We are seeking a highly skilled Principal Medical Writer to join our team at ScaleneWorks. The ideal candidate will have a strong background in clinical regulatory writing and experience in managing complex writing assignments.Key Responsibilities:Develop and execute complex writing assignments involving...

Job Title: Principal Medical Writer, Medical Writing ServicesJoin our team of experts in medical writing and content development.The Principal 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...