Responsibilities: To support the Biostatistics team by carrying out programming activities of statistical programmers and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies and publications Contributes to the overall efficiency and best practice of the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following areas: SDTM datasets, ADaM datasets, statistical tables, figures, listings, and other internal and external requests (e.g., publications) Accessing and converting data to SAS from Database management system and PC file formats (e.g., MS Excel, text files) Working with external vendors in order to develop or monitor the content and structure of SAS data sets Working closely with clinicians, statistician, and publication managers to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management review Providing input to the Database and CRF Development, creating edit check programs and providing feedback to the Data Management Providing input in developing statistical analysis plans, specifications of analysis datasets, validation plans, and other related documents Maintaining standards for programming activities Working independently to accomplish tasks and goals defined by supervisor Bringing in new ideas to improve the programming process Requirements: Minimum of bachelor's degree in related science discipline Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office Experience in CDISC data standards, e.g SDTM and ADaM Proven experience with Unix and Windows operating systems Understanding of the software development life cycle Understanding of FDA guidelines Good organization, time management and attention to detail skills needed to work in a stressful environment under tight deadlines while maintaining focus on details and quality Applies good judgment and demonstrates initiative to resolve issues Strong verbal, written and interpersonal communication skills needed to work effectively in a team environment
...gearsMinimum qualifications Knowledge of NEC codes, color codes, and American wire Minimum 5 years work experience as an Industrial Electrician NCCER or equivalent certificationPay: $34.00 - 37.00 per hour, plus per diem of $100.00 per day (must travel 60 miles to the site)...
...MOBILE CRANE OPERATOR Superior Walls Systems is seeking a Certified Mobile Crane Operator. Superior Walls Systems is a construction company that manufactures and installs precast concrete wall foundations for residential and business applications. Superior Walls...
...Job type: Part-Time (less than 20hrs/week) Location: Remote Intended Start Date: As soon as possible Who we are: Think Academy... ...Each week, more than 6 million students are enrolled in TALs online and offline education platform. Whom we are looking for:...
...Work From Home Booking Administrative Planner We are currently seeking organized and detail... ..., and vacation packages Organize and review booking details to ensure accuracy and... ...Communicate with clients via email and online platforms Assist with updates, changes...
Job Description Job Description These opportunities are located throughout Nassau County. We are seeking a Home Health Aide HHA or PCA to become a part of our team! You will provide routine home care to patients at their homes. This is a great opportunity to join a...