Get AI-powered advice on this job and more exclusive features. This range is provided by Rezolute, Inc.. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $180,000.00/yr - $195,000.00/yr Location: Redwood City, California or remote Rezolute is a late-stage rare disease company focused on significantly improving outcomes for individuals with hypoglycemia caused by hyperinsulinism (HI). Our antibody therapy, RZ358 (ersodetug), is designed to treat all forms of HI and has shown substantial benefit in clinical trials and real-world use for the treatment of congenital hyperinsulinism (cHI) and tumor hyperinsulinism (tHI). We are seeking an experienced and detail-oriented Senior Medical Writer to join our dynamic team. In this role, you will be responsible for developing high-quality, scientifically accurate, and regulatory-compliant documents for clinical trials, regulatory submissions, and medical affairs. You will collaborate with cross-functional teams, including clinical researchers, regulatory professionals, and subject matter experts, to produce materials that support the advancement of clinical trials, product development, and regulatory submissions. Responsibilities: Serves as medical writing lead on assigned projects. Works closely with in-function and cross-functional team(s) on project strategies. Implements all activities related to the preparation of writing projects. Coordinates the review, approval, and other appropriate functions involved in the production of writing projects. Negotiates with functional areas on project outcomes and deliverables to meet conflicting demands. Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or elevation as appropriate. Arranges and conducts review meetings with the team. Ensures required documentation is obtained. Scientific Writing & Documentation: Prepare and author clinical trial protocols, investigator brochures, clinical study reports, patient narratives, and regulatory submission documents (e.g., INDs, NDAs, CTDs). Develop clear, concise, and scientifically accurate documents that communicate complex medical and scientific information to both expert and non-expert audiences. Ensure compliance with regulatory guidelines, industry standards, and client specifications. Work closely with clinical, regulatory, and medical affairs teams to ensure the timely delivery of high-quality documents. Liaise with clients to understand project requirements and ensure that their expectations are met. Lead or contribute to client meetings and presentations, providing strategic advice on writing-related matters. Review & Editing: Review and edit documents prepared by junior writers, ensuring consistency, clarity, and scientific accuracy. Project Management: Manage multiple writing projects simultaneously, ensuring deadlines and quality standards are met. Identify potential challenges in document preparation and proactively address them. Research & Analysis: Conduct in-depth literature reviews to gather relevant background information. Interpret complex data from clinical trials, laboratory studies, and medical research to present findings clearly and accurately. Regulatory Knowledge: Stay up-to-date with changes in regulatory requirements, guidelines, and industry trends. Ensure that all documents comply with the latest FDA, EMA, ICH, and other relevant regulatory requirements. Qualifications: BA or higher degree. A Master’s or PhD in life sciences, pharmacology, medicine, or a related field is preferred. Minimum of 10 years of experience as a medical writer, with a focus on clinical, regulatory, or scientific writing in the pharmaceutical, biotechnology, or healthcare industries. Demonstrated experience in preparing regulatory documents and publications for submission to regulatory agencies (e.g., FDA, EMA). Strong understanding of clinical trial methodology and regulatory requirements. Excellent written and verbal communication skills. Proficient in Microsoft Word (including the use of templates), Microsoft Copilot, Excel, Adobe Acrobat, MS Project/Project Server, and PowerPoint. High attention to detail, with the ability to critically evaluate and edit scientific content. Ability to work independently and as part of a team, managing multiple priorities effectively. Preferred: Experience in writing for multiple therapeutic areas, including endocrinology, metabolism, and/or rare diseases. Knowledge of medical writing software (e.g., EndNote, Adobe Acrobat, and other document management tools). American Medical Writing Association (AMWA) certification or other is preferred, with a specialty in Editing/Writing or Pharmaceutical. Rezolute (RZLT) currently anticipates the base salary for the Senior Medical Writer role could range from $180,000 to $195,000 and will depend, in part, on the successful candidate’s geographical location and their qualifications for the role, including education and experience. This position will also be eligible for an annual performance bonus in accordance with the terms of the applicable plan. The compensation described above is subject to change and could be higher or lower than the range described based on current market survey data and the qualifications, education, experience, and geographical location of the selected candidate. Rezolute offers competitive compensation, stock options, and a rich benefits package. Qualifying employees are eligible to participate in benefit programs such as: Health Insurance (Medical / Dental / Vision) Holiday Pay Tracking Free Vacation Program Educational Assistance Benefit Fitness Center Reimbursement We are an Equal Opportunity Employer and do not discriminate against applicants due to race, ethnicity, gender, veteran status, or on the basis of disability or any other federal, state, or local protected class. Seniority level Mid-Senior level Employment type Full-time Job function Writing/Editing, Science, and Research Industries Pharmaceutical Manufacturing #J-18808-Ljbffr Rezolute, Inc.
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