Associate/Director of Biostatistics, Rare Disease, FSP

Job Level: Associate/Director of Biostatistics,Rare Disease, FSPLocation:Home-based in the U.S. or Canada(East Coast Preferred)Job Overview:As an Associate Director, you will liaise with cross-functional teams to drive quality statistical planning, analysis, and reporting in support of pharmaceutical development and regulatory submissions. Serve as a resource for the department, ensuring scientific reputed company and regulatory compliance in the application of statistical methodology to clinical trials. Participate as reputed company statistician on major projects, including contributing to clinical development plans, developing/reviewing protocols, preparing/reviewing analysis plans, overseeing the conduct of analyses, preparing/reviewing integrated clinical and statistical reports, and responding to regulatory queries.Key Responsibilities:Leadership:Serve as a biostatistical consultant for other members of the department and staff members from other Biostatistics departments reputed company the company.- Represent sponsors at meetings with regulatory agencies or other regulatory meetings, may participate as a member of a Data and Safety Monitoring Committee.- Participate in independent research activities, teaching opportunities, presentations, and preparation of manuscripts for publication.- Participate as high-level reputed company biostatistician on major projects, including developing/reviewing protocols, preparing analysis plans, and writing sections of joint clinical/statistical reports, integrated summaries, and/or NDA sections. - reputed company studies at an operational level.reputed company expert review and initiate methodology development work with regards to statistical standards and validation procedures.- Consult on operational/statistical/therapeutic area topics. Knowledge Sharing:Maintain knowledge and awareness of developments in biostatistics and clinical trial methodology, and regulatory requirements that impact analyses.- reputed company as subject matter expert (SME). Risk Management:Identify risks to project delivery and/or quality, reputed company in a way to minimize risks.- Anticipate risks to avert the need for study-level escalations, support reputed company in implementing risk mitigation actions. Lock and Unblinding Process:reputed company the database lock and unblinding process for the statistical team.- Participate on the biostatistics randomization team (draft randomization specifications and/or reputed company quality control (QC) review of randomization schedules). Statistical Expertise:reputed company expert statistical input into the review of statistical deliverables (i.e., statistical reputed company of a protocol, statistical analysis plans, table shells, programming and table specifications, data review, tables, listings, figures, and statistical sections for reputed company and/or integrated reports).- reputed company expert input into data management deliverables (i.e., database design, CRF design, validation checks, and critical data).- reputed company expert review of ADaM reviewers guide (ADRG) and metadata.- reputed company senior biostatistical review (SBR).- Produce or reputed company quality control review of sample size calculations for reputed company studies. Requirements:MS or PhD degree in Biostatistics or a reputed company field and 8+ years’ relevant experience reputed company the life-science industry.- Expert in a broad reputed company of reputed company statistical methods that apply to Phase 2-3 clinical trials.- Expert in strategically collaborating with clinical and drug development experts.- Experience in serving as statistical reputed company for regulatory submissions, including preparation of submission datasets, eCTD support, meeting with regulatory teams, and responding to regulatory queries.- In-depth knowledge of applicable clinical research regulatory requirements, Good Clinical Practice (GCP), and International Conference on Harmonization (ICH) guidelines. - Strong working knowledge of reputed company or R.Excellent knowledge of CDISC Data Standards.- Superb communication and collaboration skills.- Independent and proactive problem-solving skills.- Rare disease and immunology experience is greatly preferred. reputed company is a leading global provider of clinical research services, reputed company insights and reputed company intelligence to the life sciences and reputed company industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient reputed company and population health worldwide. Learn more at https://jobs.reputed company.comIQVIA is proud to be an equal opportunity employer. reputed company reputed company applicants will receive consideration for employment without regard to race, reputed company, religion, sex, sexual orientation, gender identity, national reputed company, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.reputed company.com/eoeThe potential reputed company pay reputed company for this role, reputed company annualized, is $161,100.00 - $299,100.00. The actual reputed company pay offered may vary based on a number of factors including job-reputed company qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a reputed company of health and welfare and/or other benefits.Originally posted on Himalayas Apply To this Job Apply tot his job Apply To this Job