The company is a global leader in partnering with companies to transform and manage their business by harnessing the power of technology.
Responsibilities:
The Manager of Statistical Programming (MSP) will stay hands-on with daily activities of a Statistical Programmer I (SP I) or Statistical Programmer II (SP II).
● Programs all tables, listings and graphs necessary for an assigned clinical study report (CSR).
● Acts as lead programmer for assigned projects.
● Programs customized data displays, (including data listings, summary tables and routine graphics) in accordance with the approved statistical analysis plan (SAP) and shell displays for clinical research studies.
● Writes code using Base SAS programs, SAS procedures, or standardized macros.
● Analyzes protocol, SAP, existing shells/templates as needed to understand structure and content of data.
● Performs data checks as needed, to ensure integrity and correctness of data displays.
● Prepares documentation for programs.
● Prepares documentation describing all datasets and variables within, including derived variables, and the project as a whole.
● Creates SAS datasets of clinical data from clinical databases.
● Creates status and efficacy datasets.
● Creates project-specific macros and formats.
● Loads client data from other platforms and other software packages.
● Prepares data to be sent to clients and as needed for other external transfers and data imports.
● Review the SAP and TLF mock-ups from programming’s perspective.
In addition to above job duties, Manager of Statistical Programming also:
● Communicates with clients to set and manage project timelines and deliverables.
● Assigns projects to the team and solves problems and/or technical difficulties.
● Trains junior team members on industry regulations, standards and internal tools used.
● Trains clients on CONFORM eClinical modules.
● Works with IT department to setup and ensure a secure environment with proper access control on SAS servers.
● Works with product development team on enhancement of CONFORM platform and process automation.
● Works with Quality Assurance team on Standard Operation Procedures drafting and revision, as well as testing and validation of CONFORM modules.
● Mentor and review the performance of members.
Qualifications:
● Ability to communicate effectively in English, in both writing and verbal.
● Ability to learn quickly and pay attention to details.
● Ability to manage multiple tasks/projects, effectively prioritize and execute tasks, and make quality and on time deliveries.
● Ability to work collaboratively, effectively, and productively in diverse organizational structures, and in interaction with dynamic clients.
● Ability to work independently, takes ownership and strives for quality and efficiency.
● Ability to work positively in a continually changing environment.
● Solid/Advanced SAS skills and understanding of the concept of standardization in data, programming, and statistical reporting of trial results and its implication to drug development.
Education an experience required:
● Master’s degree in statistics or related fields with 8+ years of industry experiences as a Statistician.
● PhD degree with 5+ years of postgraduate experiences in Biostatistics or equivalent.
● Prior experience of leading Biostatistics team.
Benefits:
● Family health plan.
● Birthday day off.
● Continuous training through content platforms.
And more!
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