Fortrea Company would like to appoint 7 employees in Kuwait for the following specializations شركة فورتريا ترغب في تعيين 7 موظفين في الكويت للتخصصات التالية

Kuwait Jobs Today: Fortria Company announces new job opportunities Are you looking for job opportunities in Kuwait? Fortria Company announces the opening of applications for many jobs in different specializations in Kuwait today. These opportunities are available to all nationalities. Learn about the available jobs and how to apply through the following advertisement. ↔️

Jobs required at Fortria Company and their details:

Senior Health Economist 

Summary of Responsibilities:

• Builds client rapport, trust and ongoing relationship, proactively identifying opportunities for new and repeat work
• Leads initial meetings with client to review work plan, timelines, data sources; leads meetings through project duration
• Leads team effort to define project scope, deliverables, budget and timelines; directs proposal writing to respond to client requirements using standard formats
• Oversees others responsible for executing on projects, ensuring data are collected according to Standard Operating Procedures (SOPs) and within agreed upon timelines and budgets; coordinates input from clients, other Fortrea groups and external advisors, and identifies scope changes and whether a change order is required.

Senior Statistical SAS Programmer 

Your responsibilities:

• Review SAPs and TFL shells from a programming perspective
• Advise on the development of complex TFL shells from a programming perspective
• Develop and/or lead the development of complex specifications for SDTMs and ADaM datasets
• Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform quality control of SDTM, ADaMs and TFLs
• Produce / define XML / PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs

Statistical Programmer – SAS & R Experience 

Your responsibilities:

• Review SAPs and TFL shells from a programming perspective
• Advise on the development of complex TFL shells from a programming perspective
• Develop and/or lead the development of complex specifications for SDTMs and ADaM datasets
• Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform quality control of SDTM, ADaMs and TFLs
• Produce / define XML / PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs
• Respond to QA and client audits and support qualification audits
• Identify and propose innovative ways to improve the efficiency, quality and productivity of our clinical statistical programming business
• Maintain awareness of industry standards, global regulatory requirements, internal guidelines and Standard Operating Procedures (SOPs)

Senior Statistical SAS Programmer, Oncology 

Your responsibilities:

• Review SAPs and TFL shells from a programming perspective
• Advise on the development of complex TFL shells from a programming perspective
• Develop and/or lead the development of complex specifications for SDTMs and ADaM datasets
• Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform quality control of SDTM, ADaMs and TFLs
• Produce / define XML / PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs
• Respond to QA and client audits and support qualification audits

Global Regulatory Submissions Lead 

Requirements (Experience, Education, Qualifications and Skills)

• Minimum 5-7 years’ experience in the Pharmaceutical industry or Drug Development in Regulatory Affairs
• Excellent communication, organization and planning skills with an attention to detail
• Extensive experience in leading clinical trial applications at a regional/global level
• Direct project management skills and ability to work independently
• Understanding of and ability to determine relevance of governmental regulatory processes and regulations as they pertain to investigational drug regulations in particular
• Bachelor’s degree or higher
• Fluency in English

Principal Statistical SAS Programmer 

Main Responsibilities:

• Plan, execute and oversee all programming activities on a study, including but not limited to: resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments, etc.
• Oversee SDTM, ADaM and TLF development, perform Senior Review of outputs
• Liaise with other Sponsor departments for additional programming needs, as required to support publications, medical writing and additional development needs and analyses
• Support/oversee submission activities (especially in late phase team)

Lead Statistical SAS Programmer, Oncology 

Main Responsibilities:

• Plan, execute and oversee all programming activities on a study, including but not limited to: resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments, etc.
• Oversee SDTM, ADaM and TLF development, perform Senior Review of outputs
• Liaise with other Sponsor departments for additional programming needs, as required to support publications, medical writing and additional development needs and analyses
• Support/oversee submission activities (especially in late phase team)

How to apply for jobs

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