Medical Writer Ii-cds

**Job Overview**: - Lead writer responsible for preparation of clinical study protocols and clinical study reports (CSRs), and other clinical documents as needed. Provides support to more experienced writers with the preparation of complex clinical documents. Interpretation of clinical, pharmacokinetic, pharmacodynamic and statistical results as...

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. Conducting operations in...

Prepares protocols and CSRs, including interpretation of clinical data and statistical results as appropriate - Work under guidance from colleagues to assist development of protocols, CSRs and other clinical documents on complex studies and programs - Prepare and review patient safety narratives - Leads project management and coordination of narrative...

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. Conducting operations in...

**Job Overview**: Lead writer independently responsible for the preparation of clinical study protocols and clinical study reports (CSRs), and other documents as needed for lower complexity studies. Provides support to more experienced writers with the preparation of clinical study protocols and CSRs, and other clinical documents as needed. Interpretation of...

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...

**Designation: Medical Writer** - Should be responsible for preparation of qualitative medical writing deliverables in any therapeutic area - Should have good experience in scientific and regulatory writing (Protocol writing, CSR, Manuscript, Abstract, Review articles and Medico-marketing inputs) - Should be able to develop LBL, Poster, News-letters, KOL...

**Designation: Medical Writer** **Workspace: On site (Mumbai)** - Should be responsible for preparation of qualitative medical writing deliverables in any therapeutic area - Should have good experience in scientific and regulatory writing (Protocol writing, CSR, Manuscript, Abstract, Review articles and Medico-marketing inputs) - Should be able to develop...

Zexcel Medical Communications Pvt Ltd **Responsibilities**: Curate and execute medical communications, collaborate on content, and oversee freelance writers. **Qualifications**: Pharmacy/Science background, 3-4 years experience, digital design skills. **CTC**: 6-8 LPA

**Job Summary**: **Key Responsibilities**: - **Content Development**: - Create, write, and edit clinical study reports, patient narratives, manuscripts, regulatory documents (such as Clinical Study Protocols, Investigator’s Brochures, and Clinical Study Reports), and other scientific documents. - **Regulatory Submissions**: Assist in the preparation of...