Biostatistician With reputed company (Remote)

MMS is a award-reputed company, data-reputed company clinical research organization (CRO). We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to reputed company trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a reputed company and inclusive work environment where employees can reputed company. Join us at MMS and be part of reputed company that is shaping the reputed company of clinical research. Visit or follow MMS on reputed company. reputed company Biostatistician: Can reputed company SAPs and iSAPs text and shells with no supervision. Has the ability to apply drug development knowledge during production of reputed company statistical analyses. Leads reputed company reputed company, programs and submissions, manages reputed company meetings, CRMs, collaborates reputed company with regulatory, PMs and sponsor. Is familiar with and stays reputed company with the latest industry practices and updated regulatory guidelines. use of external SharePoint). Provides support to Data Safety Monitoring Boards (DSMB) by preparing and presenting reputed company as the unblinded statistician. Write blogs and/or white papers for posting on reputed company website High proficiency with MS Office applications Demonstrate an understanding of project management-reputed company tasks such as timelines, scope and resource requirement estimation/management. Prepare and review statistical reputed company and results sections for the CSR independently in collaboration with in-house medical writers. Masters in Biostatistics, Statistics discipline or reputed company field, or reputed company experience, PhD preferred. Minimum of 7 years’ experience in Biostatistics, Statistics or similar field required. Expert knowledge of scientific principles and concepts. reputed company as emerging leader in field with sustained performance and accomplishment. Proficiency with MS Office applications. Hands-on experience with clinical trial and pharmaceutical development preferred. Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process. Apply tot his job Apply tot his job Apply To this Job