Medical Writer

As a highly motivated individual with a passion for communication and a desire to make a difference in the healthcare industry, you are encouraged to apply for this exciting opportunity. Your impact will involve utilizing your minimum 2 years of experience in medical writing or equivalent experience in the life sciences domain. Specifically, you will be responsible for the End-to-End authoring of periodic aggregate reports, including PBRERs, DSURs, SUSAR, PADERs/PAERs, ACOs, RMPs, and ad-hoc regulatory and safety reports. Key Responsibilities: - End-to-End authoring of periodic aggregate reports such as PBRERs, DSURs, SUSAR, PADERs/PAERs, ACOs, RMPs, and ad-hoc regulatory and safety reports - Demonstrating knowledge of regulatory documentation, drug development process, and global regulations and guidelines - Utilizing good knowledge of document management systems and other relevant applications such as Excel and Outlook Qualifications Required: - Medical/M. Pharm/Pharm D/Life sciences degree - Minimum 2 years of experience in medical writing or equivalent experience in the life sciences domain - Knowledge of regulatory documentation, drug development process, and global regulations and guidelines - Good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook) No additional details about the company were provided in the job description.,