Senior Medical Writer FULL-TIME- REMOTE

KorInsight, Inc. is looking to hire a Senior Medical Writer who will help provide full-time, remote consulting services to our biopharmaceutical client partner in the gene therapy space. Contract Duration: 6-month contract role, with opportunity to extend or convert to FTE Weekly Hours: 40 Responsibilities will include but are not limited to the following: • Write, review, and edit clinical regulatory documents such as study synopses, clinical study protocols, clinical study reports (CSRs), interim analyses, etc • Write, review, and edit regulatory and pre-clinical documents including briefing books, INDs, and related collateral documents • Critically assess and interpret statistical and clinical data • Help prepare for meetings with regulatory agencies • Work closely with cross-functional teams to ensure documents are high quality and that there is team alignment on their content and progress • Develop and carefully track timelines for document submission • Contribute to the development and implementation of medical writing best practices, policies, and SOPS to improve standards for authoring, reviewing, and finalizing documents Qualifications • Advanced degree (M.S.) in relevant scientific discipline, Doctoral level degree (Ph.D., Pharm.D., or M.D.) preferred with minimum of 3-5 years of scientific or medical writing experience at a biotech/pharmaceutical company • Familiarity with current regulatory requirements and guidelines that affect medical writing • Excellent written and verbal communication skills • Scrupulous attention to detail • Ability to simplify complex information and present it in an engaging manner • Exceptional work ethic and organizational, time, and project management skills • Ability to foster relationships, build alignment, negotiate, and collaborate with cross-functional client partners • Ability to work independently with minimal supervision Apply Job! For more such jobs please click here!