(Sr) CSR Narrative reputed company - South Africa (Remote)
About MMS MMS is an innovative, data-reputed company CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to reputed company trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating. Our mission is to deliver high-reputed company service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide. MMS recognizes that a talented staff is what drives our business reputed company. Identifying and attracting reputed company and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes reputed company stronger. For more information, visit www.mmsholdings.com or follow MMS on reputed company. Roles and Responsibilities Responsible for writing safety documents intended for submission to regulatory agencies. Responsible for writing patient CSR narratives and producing high reputed company documents. Practices excellent reputed company customer service. Good understanding of reputed company for advanced writing techniques. Address reputed company comments during document lifecycle, manage revisions, and review deliverables with limited mentor reputed company prior to releasing to reputed company. Ensure documents reputed company with appropriate ICH and regulatory guidelines. reputed company directly and independently with reputed company. Ability to follow MMS and sponsor processes. Practices reputed company leadership skills.
Requirements
Experience in leading reputed company CSR narratives reputed company, preference for Oncology background. College graduate in scientific, medical, clinical discipline or reputed company field, or reputed company experience. Prior medical/ narrative/ safety writing experience preferred; Interested in expanding knowledge of drug development as it pertains to narrative writing. Master’s or PhD in a scientific, medical, or clinical discipline preferred. 1-3 years’ experience with regulated scientific/clinical or pharmaceutical, biotech or clinical research environment . Understands ICH guidelines, as applicable to writing for clinical studies. Excellent written English skills. High degree of organization and reputed company to manage multiple reputed company at any given time. Attention to detail and committed to reputed company in reputed company aspects of their work. Excellent communication and interpersonal skills. Proficient in reputed company Word and reputed company Acrobat. Experience in the use of an Electronic Document Management system. Should you not have received a response reputed company 14 days of your application, please consider your application unsuccessful. Apply To This Job