Senior Medical Report Writer

Job Title: Cerner CCL Report Writer Location: Hyderabad Job Summary:We are looking for a skilled Cerner CCL Report Writer to join our India-based captive technology team supporting a leading global healthcare provider. In this role, you will be responsible for developing and maintaining Cerner CCL reports that support clinical, operational, and regulatory...

Company DescriptionJob Description QC and formatting of clinical trial protocols, informed consent forms (ICFs), clinical study reports (CSRs), investigator's brochures (IBs), and clinical data summaries for phase 1-phase 3 and post-marketing surveillance studies and as per agreed timelines. QC and formatting of clinical modules of eCTD dossiers for global...

Company DescriptionJob Description QC and formatting of clinical trial protocols, informed consent forms (ICFs), clinical study reports (CSRs), investigator's brochures (IBs), and clinical data summaries for phase 1-phase 3 and post-marketing surveillance studies and as per agreed timelines. QC and formatting of clinical modules of eCTD dossiers for global...

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the...

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the...

We are looking for a detail-oriented and motivated Medical Writer with an MBBS background (India or FMGE qualified/aspirants) to join our content development team. Fresh graduates passionate about transitioning into the medical content domain are welcome to apply.Key Responsibilities:Develop and review clinical course material including modules, assessments,...

JOB DETAILS 1) Lead preparation of global periodic safety reports for newly launched products. Lead coordination with GLFs to ensure information received, analyzed and incorporated into ARs as per the regulatory requirements. 2) Independent QC of ARs to ensure the information presented in AR is complete, consistent and compliant to regulatory and Hospital...

Job Responsibilities - Taking ownership and responsibility for development (write, review, proofread, and data-check) of high-quality, client-ready scientific and medical materials like manuscripts, abstracts, posters, congress and meetings materials, and literature searches and reviews according to client and audience needs with excellent a1enon to detail.-...

Job Description- As a Medical Writer at MakroCare, the role in the development and review of clinical and regulatory documents essential for the advancement of medical research and product development. Your responsibilities will include writing and reviewing a variety of documents such as clinical trial protocols, clinical study reports, investigator...

Job Description- As a member of the Global Digital Hub Team, you will play a crucial role in advancing the long-term outcomes and strategy of the Global Digital Hub, while also prioritizing the delivery of high-quality content.- In your capacity as a medical writer, you will focus on crafting medical writing and digital content solutions and focus on...