Medical Writer

Role Overview: As a Medical Writer at our company, you will play a crucial role in creating high-quality documents for various medical and scientific projects. Your expertise in scientific writing and in-depth knowledge of medical and healthcare concepts will contribute to the success of clinical trials, regulatory submissions, publications, and other scientific materials. You will collaborate closely with cross-functional teams to ensure the accuracy and compliance of all written documents. Key Responsibilities: - Write and edit various medical and scientific documents such as clinical study reports, regulatory submissions, and research papers. - Ensure that all documents adhere to regulatory requirements and company standards while maintaining clarity and accuracy. - Collaborate with researchers, clinicians, and regulatory professionals to gather essential information for document creation. - Stay informed about industry standards, medical literature, and regulatory guidelines to incorporate the latest information into your writing. - Provide scientific input to align all documents with project goals and target audiences effectively. Qualifications: - Hold a degree in Biotechnology, Pharm-D, or other relevant fields. - Demonstrate proven experience as a Medical Writer within the healthcare or pharmaceutical industry. - Possess strong writing, editing, and proofreading skills to deliver high-quality documents. - Have familiarity with medical terminology, clinical research processes, and regulatory guidelines. - Showcase the ability to work independently, meeting deadlines in a fast-paced environment. - Exhibit excellent communication and collaboration skills to work effectively with cross-functional teams. In addition, the job is full-time with a day shift schedule and requires in-person work at the specified location.,