Medical Writer

Parexel's Regulatory Medical Writing Services works closely with our clients around the world to develop and launch new medicines and treatments that improve healthcare for millions of patients. We’re one of the largest providers of medical writing services worldwide, and have managed thousands of writing projects in more than 29 countries across North and...

Parexel's Regulatory Medical Writing Services works closely with our clients around the world to develop and launch new medicines and treatments that improve healthcare for millions of patients. We’re one of the largest providers of medical writing services worldwide, and have managed thousands of writing projects in more than 29 countries across North and...

Parexel's Regulatory Medical Writing Services works closely with our clients around the world to develop and launch new medicines and treatments that improve healthcare for millions of patients. We’re one of the largest providers of medical writing services worldwide, and have managed thousands of writing projects in more than 29 countries across North and...

The Publications and Scientific Communications team, a part of Medical Writing and Healthcare Communications at Evidera, prepares medical publications, abstracts, posters, presentations, and other scientific communications. Our dynamic, highly collaborative team focuses on providing quality writing to internal collaborators and external pharmaceutical and...

Medical Writer Intern - Health Blogging Location: Always Remote Duration: 6 Months Internship Education Requirement: Current Students Pursuing a Degree in Life Sciences (MBBS, BDS, BAMS, BHMS, B.Sc Nursing, B.Sc Zoology, B.Sc Botany, B.Sc Biotechnology, or other relevant life science fields) **Job Types**: Part-time, Fresher **Salary**: ₹6,000.00 per...

Job DescriptionProvides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. Demonstrates subject matter and therapeutic area expertise. May assist program manager. Collaborates with internal and external clients, supporting and enabling effective and efficient...

Job DescriptionProvides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. Demonstrates subject matter and therapeutic area expertise. May assist program manager. Collaborates with internal and external clients, supporting and enabling effective and efficient...

Parexel's Regulatory Medical Writing Services works closely with our clients around the world to develop and launch new medicines and treatments that improve healthcare for millions of patients. We’re one of the largest providers of medical writing services worldwide, and have managed thousands of writing projects in more than 29 countries across North and...

Content Writer Experience: 2-5 years **Salary**: 6-8.50 LPA JD of the position is - Craft a cohesive content strategy across our blog, social media, and communities - Write high-quality, SEO-friendly blog posts about common healthcare conditions women face and treatment options. Note: We can provide basic SEO guidelines. - Ensure information is medically...

Clinical Trial Protocol SpecialistThe Clinical Trial Protocol Specialist will research, create, and edit clinical trial protocols as well as provide expert support for protocol development.Operates as a lead medical writer or as a Subject Matter Expert (SME) to support Medical Writers and Clinical Trial Services management, as well as other Parexel...

Job DescriptionSummarized Purpose: Provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. Demonstrates subject matter and therapeutic area expertise. May assist program manager. Collaborates with internal and external clients, supporting and enabling effective and...

Job DescriptionSummarized Purpose: Provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. Demonstrates subject matter and therapeutic area expertise. May assist program manager. Collaborates with internal and external clients, supporting and enabling effective and...

Job Purpose: Responsible for management of scheduled and unscheduled aggregate reports including but not limited to Periodic Safety Reports (PSRs) including Periodic Safety Update Reports (PSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs), Addendum to Clinical Overviews (ACOs), Semi-Annual Safety Reports (SASRs), Corporate Addendum Reports, United...

**JOB DESCRIPTION - SEO WRITER** (0-1 Years) **About us**: Text Mercato is a company that specializes in developing high-quality content for its clients using a proprietary platform and advanced algorithms that allow for efficient delivery within set timeframes. One of the company's strengths is its ability to maintain consistent quality while scaling its...

Job Title**:Copywriter/Content Writer | Sector - Pharma/Medical/Healthcare** Location**:Remote/In-Office** **Company Overview**: We're a versatile creative agency specializing in design and film production across various industries. Our team thrives on crafting captivating narratives and visuals that leave a lasting impact. Currently, we're seeking a...

Providing high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. - Collaborating with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence. - Serving as primary author who writes and provides...

Job Description• Serves as primary author who writes and provides input on routine documents such as clinical study reports and study protocols, and summarizes data from clinical studies.• Ensures compliance with quality processes and requirements for assigned documents. May assist in determining best practices, methods and techniques for achieving...

Job Description• Serves as primary author who writes and provides input on routine documents such as clinical study reports and study protocols, and summarizes data from clinical studies.• Ensures compliance with quality processes and requirements for assigned documents. May assist in determining best practices, methods and...

Summarized Purpose: Responsible for the planning, coordination and delivery of safety writing services for multiple clinical trial and/or marketed product projects. Performs day-to-day safety writing and related activities within a highly regulated pharmacovigilance environment, driven by strict timelines. Activities include but are not limited to delivery...

Hims Hers is looking for a Public Relations/Communications Manager that can make a significant impact on our business A successful candidate views communications as a business driver and has a proven track record leveraging communications strategies to achieve business goals, specifically in increasing SEO E-A-T signals, like topical authority The role...