Clinical Trial Medical Writer

We are looking for a skilled Clinical Trial Medical Writer!Experience: 3+ years working in the field of clinical trial medical writingDevelop case report formats, protocol letters, and record forms crucial for clinical trialsPrepare all required documentation for the initiation, execution, and completion of clinical trialsConduct literature reviews and...

Experience: 3+ years in clinical trial medical writingResponsibilities:Develop case report formats, protocol letters, and record forms essential for clinical trials.Prepare all necessary documentation for clinical trial initiation, execution, and completion.Conduct literature reviews and data analysis to support trial design and manuscript development.Draft...

Experience: 3+ years in clinical trial medical writingResponsibilities:Develop case report formats, protocol letters, and record forms essential for clinical trials.Prepare all necessary documentation for clinical trial initiation, execution, and completion.Conduct literature reviews and data analysis to support trial design and manuscript development.Draft...

Experience: 3+ years in clinical trial medical writing   Responsibilities:   Develop case report formats, protocol letters, and record forms essential for clinical trials. Prepare all necessary documentation for clinical trial initiation, execution, and completion. Conduct literature reviews and data analysis to support trial design and manuscript...

Experience: 3+ years in clinical trial medical writing Responsibilities: Develop case report formats, protocol letters, and record forms essential for clinical trials.Prepare all necessary documentation for clinical trial initiation, execution, and completion.Conduct literature reviews and data analysis to support trial design and manuscript...

Experience: 3+ years in clinical trial medical writing Responsibilities: Develop case report formats, protocol letters, and record forms essential for clinical trials.Prepare all necessary documentation for clinical trial initiation, execution, and completion.Conduct literature reviews and data analysis to support trial design and manuscript...

Experience: 3+ years in clinical trial medical writing   Responsibilities:   Develop case report formats, protocol letters, and record forms essential for clinical trials. Prepare all necessary documentation for clinical trial initiation, execution, and completion. Conduct literature reviews and data analysis to support trial design and manuscript...

Labcorp Drug Development As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired...

**We are Growing**! Let us support your career journey the Biorasi way. Innovative, Collaborative, Dynamic and Evolving. Capitalizing on your strengths while encouraging work-life balance. Biorasi is an award-winning, customer-focused, full-service clinical research organization, and we are unlike any CRO you’ve ever heard of. Biorasi is looking for top...

**Medical Writer - Clinical**: - From 2 to 3 year(s) of e - Contact Company:_Alkem Laboratories - Address:_Alkem Laboratories, Taloja Police Station, C-6/1 C-6/2 C-17/7, Dist, Industrial Estate, Taloja, Navi Mumbai, Maharashtra 410208 - Reference Id:_Medical Writer 1

105,000 people reimagining medicine for more than 766 million people globally. To provide country clinical strategic guidance and feasibility assessment for GDD trials. Your responsibilities include, but are not limited to - To provide clinical strategic and tactical leadership in the country to support GDD trials, clinical development plans which change the...

100,000+ That’s how many patients participate in our clinical trials at any given time. GCO is Novartis’ powerhouse of Global Clinical Operations, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link between science and medicine -...

**Essential Job Duties**: 1) Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support 2) Assist in the preparation of study and site specific materials in accordance with relevant SOPs 3) Complete minute taking and documentation for sponsor/external or internal teleconferences...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

As a medical writer, you will be responsible for writing documents, articles, journals, brochures, and product manuals for our organization. You will cover topics in clinical trials, treatments, procedures, medical devices, pharmaceutical drugs, medical research/breakthroughs, and other educational materials. Roles and Responsibilities - Write and edit...

393172BR **Clinical Research Medical Advisor**: India **About the role** Novartis is a pioneer in drug development with a robust pipeline across therapy areas. CRMAs work closely with Investigators and ensure scientific engagement with the Investigator community to drive our programs and trials across the globe. Your responsibilities include, but are not...

Mumbai, Andheri East - Medical Content Writer/ Doctor of Pharmacy/ - Required: 10 Content Writers - Job location Andheri East Mumbai Maharashtra Research of online drug and medical databases. - Creation of medical information content for Active pharmaceutical ingredients, general products (OTC). - Content creation for various surgical and laboratory...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Clinical trials are the actual experimental studies in which human volunteers are included, after their consent, to test new treatments, instruments,Read More

ICON plc is a leading healthcare intelligence and clinical research company. We take pride in creating a diverse and innovative work environment, and we invite you to be part of our journey to influence the future of clinical development.Clinical Trial AssistantLocation : Mumbai, On-siteResponsibilities:- Document collection and submission support- Vendor...