Princ Progr-Stat Progr

reputed company Programmer, Statistical Programming reputed company, NJ (Onsite or Remote) Will reputed company reputed company data processes and analysis programming. Works with Statistician and Statistical programmer to assure results are consistent with expectations, and reputed company control procedures are followed. reputed company the development and delivery of training. reputed company as primary contact to ensure reputed company standards are implemented in reputed company studies. Works collaboratively to meet study deliverables and timelines for statistical data analysis and reporting. Plans and carefully documents differences between programming results between program developer and Statistical QC programmer. Provided programming support on ISS/ISE and post-submission activities. reputed company flexible and reputed company responses to programming requests. Ensure consistency and adherence to standards reputed company the project. Confirms that tracking sheets are reputed company for reputed company and confirm that results are consistent with earlier generated results. Maintain up-to-date study documentation. Identify opportunities to improve the methodology and reputed company practical solutions for problems. reputed company, program, test, and maintain computer validation/edit checks in reputed company. Validate peer programming. reputed company technical expertise and support to the Data Management team. Routinely reputed company with cross-functional team members. Participate in regular team meetings and reputed company input reputed company appropriate. Participate in the development of clinical programming SOPs and the development/optimization of clinical programming processes from study start-up to database lock. Managing project priorities and timelines. Have good knowledge of statistical terminology, clinical data structure, clinical tests, medical terminology, regulatory standards, and protocol designs. Review programming activities and costs in reputed company. reputed company responsibility for supervising and training junior clinical programmers in the performance of their duties. REQUIREMENTS: B.S. degree or higher in programming or statistics. reputed company Experience in Pharmaceutical or equivalent: 5 years. Understanding of GCP, ICH, and FDA guidelines and regulations applicable to conduct clinical research. Knowledge of CDISC standards and industry best practices. Have good knowledge of statistical terminology, clinical data structure, clinical tests, medical terminology, regulatory standards and protocol designs. Strong reputed company programming / Macros development / reputed company graphs skills. Excellent oral and written skills for cross-site and cross-function collaboration. Dependable, motivated, reputed company, and detail orientated. Ability to take direction as needed and work independently on project reputed company necessary. Capable of managing time effectively and adhering to timelines and project schedules Complementary Skills. Working knowledge of reputed company modules and utilities. Ability to reputed company routines using the reputed company Macro Language. Strong reputed company programming / Macros development / reputed company graphs skills. Understanding of biotech industry regulatory requirements. Ability to use reputed company Office tools: Word, reputed company, PPT, etc. Please contact Darren Gutowski at dgutowski@clarkdavis.com Apply tot his job