Company Fortrea opens its doors to those interested in obtaining exceptional job opportunities in Bahrain
If you are interested, check out the following details:
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Overview
- Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network.
- Our talented and diverse team of approximately 19,000 people working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
Vacant Positions:
Statistical SAS Programmer II - Sponsor Dedicated (FSP)
Your Responsibilities:
- With sufficient experience assume the role of a Lead Statistical Programmer for CP studies only with support from senior programming staff
- 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 and the client, etc.
- Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform QC of SDTM, ADaMs and TFLs
- Produce Define XML/PDFs, Analysis Results Metadata (ARM), annotated eCRFs and Reviews Guides to support SDTMs and ADaMs
- With support from senior programming staff, develop specifications for SDTMs and ADaM datasets
- Review SAPs and TFL shells from a programming perspective for studies with support from senior programming staff
- Respond to QA and client audits with support from senior programming staff
Principal Statistical SAS Programmer - Sponsor Dedicated (FSP)
Your 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)
- Ensure all activities are conducted efficiently, with appropriate set-up of needed tools and macros, prioritizing quality at all times
- Mentor less-experienced team members in best practices around SDTMs, ADaMs and TFLs while ensuring adherence to department standards and processes
Lead Statistical SAS Programmer - Sponsor Dedicated (FSP)
Your 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)
- Ensure all activities are conducted efficiently, with appropriate set-up of needed tools and macros, prioritizing quality at all times
- Mentor less-experienced team members in best practices around SDTMs, ADaMs and TFLs while ensuring adherence to department standards and processes
Principal Statistical SAS Programmer - Multi Sponsor
Your 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
- Ensure all activities are conducted efficiently, with appropriate set-up of needed tools and macros, prioritizing quality at all times
- Mentor less-experienced team members in best practices around SDTMs, ADaMs and TFLs while ensuring adherence to department standards and processes
Senior Statistical SAS Programmer - Multi Sponsor
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)
Statistical Programmer II - Multi Sponsor
Your Responsibilities:
- With sufficient experience assume the role of a Lead Statistical Programmer for CP studies only with support from senior programming staff
- 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 and the client, etc.
- Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform QC of SDTM, ADaMs and TFLs
- Produce Define XML/PDFs, Analysis Results Metadata (ARM), annotated eCRFs and Reviews Guides to support SDTMs and ADaMs
- With support from senior programming staff, develop specifications for SDTMs and ADaM datasets
- Review SAPs and TFL shells from a programming perspective for studies with support from senior programming staff
- Respond to QA and client audits with support from senior programming staff
Your Profile:
- Minimum Bachelor’s degree, preferably in mathematics, statistics, computing, life science, health science, or related subjects
- Typically, 1 - 2 years of SAS® programming experience in the CRO or Pharmaceutical industry, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job
Lead Statistical SAS Programmer - Multi Sponsor
Your 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)
- Ensure all activities are conducted efficiently, with appropriate set-up of needed tools and macros, prioritizing quality at all times
- Mentor less-experienced team members in best practices around SDTMs, ADaMs and TFLs while ensuring adherence to department standards and processes
Your Profile:
- Ideally, a degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc.
- In lieu of the above: professional experience in statistical programming within clinical trials in a biotech, CRO or pharmaceutical company
- Solid experience with complex clinical trials (minimum 5 years) and the corresponding datasets’ content (safety and efficacy) and endpoints
- Previous Lead experience preferred
- Ideally you will have knowledge in all aspects of clinical trials, from initial study set-up to study completion, with an understanding of the roles and responsibilities of all related disciplines, e.g. Biostatistics and Clinical Data Management
Application Steps:
- Open the application link
- Browse the available jobs and select the one that suits you.
- Click on "Apply Now" and enter the required information.
- Ensure that your details are entered correctly, then click "Submit".
Additional Details:
- Source: linked in
- Posting Date: 27/1/2025
- Required Nationalities:
- Required Nationalities: All nationalities
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