Summary of Responsibilities:
- With sufficient experience assume the role of a Lead Statistical Programmer 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 analysis datasets and TFLs perform validation of analysis datasets and TFLs.
- With support from senior programming staff develop specifications for analysis datasets and TFLs.
- 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.
- All other duties as needed or assigned.
Qualifications (Minimum Required):
- Bachelors degree preferably in mathematics statistics computing life science health science or related subjects.
- Experience and/or education plus relevant work experience equating to a Bachelors degree.
- Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
- Language Skills Required:fluent in English both written and verbal
Experience (Minimum Required):
- Typically 1 - 2 years of SAS programming experience in the CRO medical device or pharmaceutical industry or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
- Knowledge of CDISC requirements a plus.
Physical Demands/Work Environment:
- Office or home-based environment as requested by the line manager.
- Travel Requirements: local domestic regional - approximately 5% of the time.
- Travel is primarily to where: client meetings and trainings.
Learn more about our EEO & Accommodations request here.
Required Experience:
IC
Summary of Responsibilities:With sufficient experience assume the role of a Lead Statistical Programmer 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 m...
Summary of Responsibilities:
- With sufficient experience assume the role of a Lead Statistical Programmer 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 analysis datasets and TFLs perform validation of analysis datasets and TFLs.
- With support from senior programming staff develop specifications for analysis datasets and TFLs.
- 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.
- All other duties as needed or assigned.
Qualifications (Minimum Required):
- Bachelors degree preferably in mathematics statistics computing life science health science or related subjects.
- Experience and/or education plus relevant work experience equating to a Bachelors degree.
- Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
- Language Skills Required:fluent in English both written and verbal
Experience (Minimum Required):
- Typically 1 - 2 years of SAS programming experience in the CRO medical device or pharmaceutical industry or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
- Knowledge of CDISC requirements a plus.
Physical Demands/Work Environment:
- Office or home-based environment as requested by the line manager.
- Travel Requirements: local domestic regional - approximately 5% of the time.
- Travel is primarily to where: client meetings and trainings.
Learn more about our EEO & Accommodations request here.
Required Experience:
IC
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