Medical Writer

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...

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...

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 Hiring *******************************Work Location: AIG Hospital, GachibowliInterview Location: Writer Information, KukatpallyEmployment Type: Full-timeInterview Details:Venue: Writer Information, KukatpallyDate & Time: 22-Aug-25 to 23-Aug-25 [11am to 2PM]Contact Person: [HR Vinay]Landmark : 8th FLOOR, Vijay Sai Towers, opp....

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 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...

About this Opportunity:We are seeking an Associate Project Specialist to support our Medical Communications team. This role will be responsible for providing project management support to scientific writers, ensuring the effective delivery of medical education and publication projects.

We are seeking an experienced and detail-oriented Medical Reviewer to join our team. The role involves reviewing, analyzing, and ensuring accuracy, consistency, and compliance of medical and scientific content in alignment with regulatory, clinical, and organizational standards.Key ResponsibilitiesReview medical, clinical, and regulatory documents for...