الوصف الوظيفي
Duties and Responsibilities
Performs his/her duties and tasks as per Hospital Policy and Agreement on Professional Code of Conduct.
Actively participates in all quality and performance improvement activities within the department/service and within the hospital as per Quality Improvement and Patient Safety Plan.
Actively participates in all the education requirement and activities as per the Hospital Education Program.
Performs other applicable tasks and duties assigned within the scope of practice and employment contract.
Directly responsible for the data integrity, adequacy, accuracy and confidentiality of the hospital data/information and research projects whether quantitative, qualitative or both.
Responsible for ensuring the statistical validity by solving problems occurring in the data collection process.
Design and create various dashboards based on department request.
Evaluates sources of information in order to determine any limitations in terms of reliability or usability.
Provides electronic critical review of clinical or non-clinical data reports, integrated summary documents and external publications.
Serve as back-up support for any required statistical function in the department.
Analyze and interpret electronic statistical data in order to identify significant differences in relationships among sources of information.
Evaluate the statistical methods and procedures used to obtain data in order to ensure validity, applicability, efficiency and accuracy.
Observing, receiving and otherwise obtaining information from all relevant sources.
Logs, tracks and documents all successful and unsuccessful work orders and actions taken, through Track-It modules of the department.
Maintains work ethics by preserving the confidentiality and sensitive information encountered in the course of professional activities and personal integrity.
Report results of statistical analyses, including information in the form of graphs, charts and tables. Which will be generated by dashboard?
Participate in the daily presentation activities and regular/departmental meetings within the department for staff advancement.
Providing statistical programming and validation support for clinical study reports, overseeing programming activities by KFMMC. When necessary and coordinating programming activities among the study programmers to achieve timely progress in the following areas: analysis and other datasets, statistical tables, figures, listings, integrated, progress reports, electronic submissions, QLICK and other internal and external request. Accessing and other converting data to SAS or PowerBI 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.
Providing input in developing statistical analysis plans, producing specifications of analysis plans, producing specifications of analysis datasets, validation plans, and other related documents. Good understanding with different phases of clinical trials, protocols.
Maintaining standards for programming activities (directory structure, etc.) and guiding/ coaching statistical programmers.
Working independently as well as in teams to accomplish tasks and goals defined by supervisor. Attending required training and meetings and bringing in new ideas to improve the programming process.
Design and develop systems and application to manage the department information according to the collected data.
المهارات
Minimum of one (1) year experience in SQL programming department environment for clinical purposes with visual studio, C#, and additional courses in statistics
Good understanding in various software such as QLICK, POWERBI packages.
Good Experience in Database Management System (DBMS) and Basic Knowledge of Programming.
Good understanding of regulatory guidelines in a healthcare research setting.
Good knowledge of statistical software- excel and other related packages.
Preferably with proven research publications.
Good managerial/ technical understanding of programming and clinical isolated
issues along with ability to demonstrate significant leadership of SAS or SQL
programming technical activities in clinical pharmaceutical environment define
.XML knowledge and familiarity with submission process is preferred.
Good understanding of the software development life cycle.
Good experience using MS-SQL, Oracle SQL, SAS-Base, PowerBI, MACRO
STAT, GRAPH, ACCESS and MS office.
In depth knowledge in SAS and/or R.
Python Coding.
Hadoop platform.
SQL database/ coding.
Working with unstructured data.
Excellent written, verbal communication and presentation skills to convey information effectively.
Excellent interpersonal skills.
Detail-oriented with excellent organizational and problem-solving skills.
Ability to work effectively in a team environment.
Strong organizational skills with ability to prioritize effectively.
Ability to work independently or with limited supervision.
Skilled using application software/ tools.
Skilled in evaluation of documentation
Good numerical/ analytical skills
Good organization, time management and attention to detail skills needed to work in a stressful environment under tight deadlines while remaining focus on details and quality.
Ability to applies good judgment and demonstrates initiative to resolve issues. proactive and effective working.
Willingness to learn and work on new programs and being up to date with the existing ones.
Education
Computer Science or a related science discipline
تفاصيل الوظيفة
منطقة الوظيفة الدمام, المملكة العربية السعودية
قطاع الشركة الإدارة العامة
طبيعة عمل الشركة صاحب عمل (القطاع الخاص)
الدور الوظيفي تكنولوجيا المعلومات
نوع التوظيف دوام كامل
الراتب الشهري غير محدد
عدد الوظائف الشاغرة 1
https://www.bayt.com/ar/saudi-arabia/jobs/مبرمج-بيانات-data-programmer-4677831/
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