IQVIA
IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research
Responsibilities:
Import data from various sources
Program quality control checks for source data and reporting data issues
Interpret project level requirements and develop programming specifications
Write programming code following established Good Programming Practices
Program SDTM and ADaM datasets
Program to create statistical analysis tables, listing and figures
Validate datasets and all statistical outputs per prescribed gate checks
Communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and timelines
Use and promote the use of established standards, SOPs, and standard methodologies
Export data and clinical study report materials
Provide training and mentoring to team members and department staff
You can help us bring clinical trial statistical analysis into the next generation. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects across therapeutic areas. Be challenged in a fast-paced team environment that is collaborative in performing biostatistical analyses and advanced statistical programming. Development opportunities and mentoring at all levels enable you to progress your long-term career in the direction you choose.
THE PERSON
We know that meaningful results require not only the right approach, but also the right people. Candidates should possess a Master’s or Bachelor’s degree in Biostatistics, Statistics, Mathematics, or Computer Science, and have a strong educational or practical evidence in programming.
Key required skills include:
Home Based/Remote
5+ experience in Statistical Programmer role from CRO/Pharma with ADaM/SDTM/ TLFs
Excellent accuracy, attention to detail, problem solving, organizational as well as interpersonal communication.
In light of the above, candidates for the roles should exhibit the following skills and competencies:
Experience in programming in SAS within the CRO/Pharma/Biotech/Healthcare industries
Knowledge of statistics and exhibit routine and occasionally complex analytical skills
A focus on quality, accuracy, and completeness of work activities
Excellent communication skills
A good understanding of Good Clinical Practice and ICH guidelines
Ability to independently lead (or have lead potential) and estimate programming scope of work, handle resource assignments, communicate work status, and work within project timelines for deliverables
Take initiative and can be counted on to get the job done, with integrity
Have the self-awareness to recognize when negotiating skills and assistance are needed
Ability to establish and maintain effective working relationships with co-workers, managers, and clients
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