PSG Global Solutions Careers
Senior Biostatistical Programmer
PSG Global Solutions Careers, Woodcliff Lake, New Jersey, us, 07677
Apply now and our proprietary system will quickly have you in front of a live recruiter.The OpportunityDescriptionWe're looking for a
Senior Biostatistical Programmer , working in
Pharmaceuticals and Medical Products
industry in
Woodcliff Lake, New Jersey, 07677, United States .
Provides statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following areas: SDTM datasets, ADaM datasets, statistical tables, figures, listings,and other internal and external requests (e.g., publications).Works with external vendors in order to develop or monitor the content and structure of SAS data sets.Works closely with clinicians, statistician, and publication managers to generate and QC outputs for publications; reviews publication (abstract/ manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinates internal resource utilization for publication and generate activities metrics for management review.Provides input to the database and CRF development, creating edit check programs and providing feedback to the data management.Provides input in developing statistical analysis plans, specifications of analysis datasets, validation plans, and other related documents.
Our Client
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Bachelors degree in Statistics, Computer Science, Mathematics, or a related science discipline (Masters degree preferred)10+ years of experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environmentFDA submission experience preferredSome project experience in a pharmaceutical/CRO programming environment or demonstrated leadership in a clinical pharmaceutical/CRO environmentExperience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS OfficeExperience in CDISC data standards, e.g. SDTM and ADaMProven experience with Unix and Windows operating systemsUnderstanding of the software development life cycleUnderstanding of FDA guidelines
What Do You Think?Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?
Senior Biostatistical Programmer , working in
Pharmaceuticals and Medical Products
industry in
Woodcliff Lake, New Jersey, 07677, United States .
Provides statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following areas: SDTM datasets, ADaM datasets, statistical tables, figures, listings,and other internal and external requests (e.g., publications).Works with external vendors in order to develop or monitor the content and structure of SAS data sets.Works closely with clinicians, statistician, and publication managers to generate and QC outputs for publications; reviews publication (abstract/ manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinates internal resource utilization for publication and generate activities metrics for management review.Provides input to the database and CRF development, creating edit check programs and providing feedback to the data management.Provides input in developing statistical analysis plans, specifications of analysis datasets, validation plans, and other related documents.
Our Client
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Bachelors degree in Statistics, Computer Science, Mathematics, or a related science discipline (Masters degree preferred)10+ years of experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environmentFDA submission experience preferredSome project experience in a pharmaceutical/CRO programming environment or demonstrated leadership in a clinical pharmaceutical/CRO environmentExperience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS OfficeExperience in CDISC data standards, e.g. SDTM and ADaMProven experience with Unix and Windows operating systemsUnderstanding of the software development life cycleUnderstanding of FDA guidelines
What Do You Think?Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?