SynteractHCR is a full service, international CRO. Since 1987, we have been guiding virtual, emerging, and mid-sized biopharma companies across the spectrum of Phase I – IV clinical studies with support services that address their specific needs.
If you have clinical research, biotech or pharmaceutical experience and you are seeking a new Biostatistics opportunity we’d like to speak with you. Our positions are located in our Carlsbad office, and may have the ability to work from home 1-2 days per week. To apply to any of our opportunities, visit www.synteracthcr.com/careers today!
Senior/Principle Biostatistician:
The Senior/Principal Biostatistician performs the data analysis with supervision for assigned clinical studies. Works closely with the clinical team, project Sponsor, data manager, other Biostatisticians and programmers to analyze and present the data based on Sponsor specifications. He/she writes/reviews the study protocol, develops statistical analyses plan, performs statistical analyses, writes statistical results, and writes/reviews the clinical study report. Responsibilities include leading projects and coordinating/monitoring other Biostatistician deliverables, creating/maintaining analyses, tables/listings/figures, writing/reviewing Statistical Analysis Plan (including Mock tables/listings), writing/reviewing Clinical study reports (CSRs), reviewing Case Report Forms for assigned projects, ensuring table, listing and statistical analysis programming is being done according to Sponsor specifications, etc.
Requirements include Master's degree or equivalent in statistics, mathematics or related field of project with a minimum of 5 to 7 years of clinical trials research experience or PhD in statistics with a minimum of 2 to 5 years related experience and advanced proficiency in BASE SAS, or other statistical software is advantageous, understands the sequence of running programs to ensure up-to-date data and to troubleshoot, debug programming problems and to identify data trends, nonverbal symbolism experience (formulas, scientific equations, graphs, musical notes, etc.,) in its most difficult phases, and effective verbal and writing skills.
Senior Manager, Statistical Programming:
The Senior Manager, Statistical Programming manages the day to day activities of Statistical Programmers, responsible for providing programming support to the biostatistics and clinical programming functions. Additionally performs the data analysis for assigned clinical studies. Works closely with the project team, Sponsors and vendors to analyze and present the data based on Sponsor specifications. He/she develops, creates, verifies/validates and maintains managing the programs for assigned projects. Responsibilities include creating/maintaining analyses, tables/listings/figures, performing programming validation/QC, creating specifications for, and program derived datasets, providing ad-hoc reports, assisting in programming edit checks, working with Sponsor/statistician to review SAP, including mock tables and listings, mentor/train and provide guidance to other statistical programmers, leads specialized Biostatistics development projects as requested by Management, may generate randomization schedules, management responsibilities require one to assist with hiring and assimilating employees; to provide on-going feedback and development; to document and deliver annual performance reviews; to coach, counsel and make determination of involuntary separation of employees as appropriate.
Requirements include Bachelor or Master degree in mathematics, statistics, or related field of study and 8+ years of experience, or equivalent combination of education and experience and 1-2 years’ experience effectively managing results in terms of costs and/or methods and employees.
Senior/Principle Statistical Programmer:
The Senior/Principal Statistical Programmer provides programming support with supervision to the biostatistics and clinical programming functions. Develop, create, verify/validate and maintain managing the programs for assigned projects. Responsibilities include creating/maintaining analyses, tables/listings/figures, performing programming validation/QC, creating specifications for, and program derived datasets, providing ad-hoc reports as requested, assists in programming edit checks, mentor/train and provide guidance to other statistical programmers, leads projects and performs senior level reviews, develops macros, time estimates and will carry out problem solving, supports the departmental training process, etc.
Requirements include Bachelor's degree or equivalent in mathematics, statistics, or related field of study and a minimum of 5+ years Statistical Programming experience, or equivalent combination of education and experience, with advance proficiency in BASE SAS, SPSS or other statistical software, understands the sequence of running programs to ensure up-to-date data and to troubleshoot, debug programming problems and to identify data trends, good verbal and written communication, and proficiency in MS-Office as required by the role.
Statistical Programmer II:
The Statistical Programmer II provides programming support with supervision to the biostatistics and clinical programming functions. He/she develops, creates, verifies/validates and maintains the programs for assigned projects in compliance with standard operating procedures. Responsibilities include creating/maintaining analyses, tables/listings/figures, creating specifications for, and program derived datasets, providing ad-hoc reports as requested, assisting in programming edit checks, working with Sponsor/statistician to review SAP, including mock tables and listings, may train and provide guidance to other statistical programmers, and may provide comments and suggestions on internal SOPs and training instructions.
Requirements include Bachelor's degree or equivalent in mathematics, statistics, or related field of project, minimum of 2 years of Statistical Programming experience or equivalent combination of education and experience, working knowledge of GCPs, ICH guidelines, FDA and other applicable country regulations, proficiency in BASE SAS, SPSS or other statistical software, understands the sequence of running programs to ensure up-to-date data and to troubleshoot, debug programming problems and to identify data trends, and Nonverbal symbolism experience (formulas, scientific equations, graphs, musical notes, etc.,) in its most difficult phases.
If you have clinical research, biotech or pharmaceutical experience and you are seeking a new Biostatistics opportunity we’d like to speak with you. Our positions are located in our Carlsbad office, and may have the ability to work from home 1-2 days per week. To apply to any of our opportunities, visit www.synteracthcr.com/careers today!
Senior/Principle Biostatistician:
The Senior/Principal Biostatistician performs the data analysis with supervision for assigned clinical studies. Works closely with the clinical team, project Sponsor, data manager, other Biostatisticians and programmers to analyze and present the data based on Sponsor specifications. He/she writes/reviews the study protocol, develops statistical analyses plan, performs statistical analyses, writes statistical results, and writes/reviews the clinical study report. Responsibilities include leading projects and coordinating/monitoring other Biostatistician deliverables, creating/maintaining analyses, tables/listings/figures, writing/reviewing Statistical Analysis Plan (including Mock tables/listings), writing/reviewing Clinical study reports (CSRs), reviewing Case Report Forms for assigned projects, ensuring table, listing and statistical analysis programming is being done according to Sponsor specifications, etc.
Requirements include Master's degree or equivalent in statistics, mathematics or related field of project with a minimum of 5 to 7 years of clinical trials research experience or PhD in statistics with a minimum of 2 to 5 years related experience and advanced proficiency in BASE SAS, or other statistical software is advantageous, understands the sequence of running programs to ensure up-to-date data and to troubleshoot, debug programming problems and to identify data trends, nonverbal symbolism experience (formulas, scientific equations, graphs, musical notes, etc.,) in its most difficult phases, and effective verbal and writing skills.
Senior Manager, Statistical Programming:
The Senior Manager, Statistical Programming manages the day to day activities of Statistical Programmers, responsible for providing programming support to the biostatistics and clinical programming functions. Additionally performs the data analysis for assigned clinical studies. Works closely with the project team, Sponsors and vendors to analyze and present the data based on Sponsor specifications. He/she develops, creates, verifies/validates and maintains managing the programs for assigned projects. Responsibilities include creating/maintaining analyses, tables/listings/figures, performing programming validation/QC, creating specifications for, and program derived datasets, providing ad-hoc reports, assisting in programming edit checks, working with Sponsor/statistician to review SAP, including mock tables and listings, mentor/train and provide guidance to other statistical programmers, leads specialized Biostatistics development projects as requested by Management, may generate randomization schedules, management responsibilities require one to assist with hiring and assimilating employees; to provide on-going feedback and development; to document and deliver annual performance reviews; to coach, counsel and make determination of involuntary separation of employees as appropriate.
Requirements include Bachelor or Master degree in mathematics, statistics, or related field of study and 8+ years of experience, or equivalent combination of education and experience and 1-2 years’ experience effectively managing results in terms of costs and/or methods and employees.
Senior/Principle Statistical Programmer:
The Senior/Principal Statistical Programmer provides programming support with supervision to the biostatistics and clinical programming functions. Develop, create, verify/validate and maintain managing the programs for assigned projects. Responsibilities include creating/maintaining analyses, tables/listings/figures, performing programming validation/QC, creating specifications for, and program derived datasets, providing ad-hoc reports as requested, assists in programming edit checks, mentor/train and provide guidance to other statistical programmers, leads projects and performs senior level reviews, develops macros, time estimates and will carry out problem solving, supports the departmental training process, etc.
Requirements include Bachelor's degree or equivalent in mathematics, statistics, or related field of study and a minimum of 5+ years Statistical Programming experience, or equivalent combination of education and experience, with advance proficiency in BASE SAS, SPSS or other statistical software, understands the sequence of running programs to ensure up-to-date data and to troubleshoot, debug programming problems and to identify data trends, good verbal and written communication, and proficiency in MS-Office as required by the role.
Statistical Programmer II:
The Statistical Programmer II provides programming support with supervision to the biostatistics and clinical programming functions. He/she develops, creates, verifies/validates and maintains the programs for assigned projects in compliance with standard operating procedures. Responsibilities include creating/maintaining analyses, tables/listings/figures, creating specifications for, and program derived datasets, providing ad-hoc reports as requested, assisting in programming edit checks, working with Sponsor/statistician to review SAP, including mock tables and listings, may train and provide guidance to other statistical programmers, and may provide comments and suggestions on internal SOPs and training instructions.
Requirements include Bachelor's degree or equivalent in mathematics, statistics, or related field of project, minimum of 2 years of Statistical Programming experience or equivalent combination of education and experience, working knowledge of GCPs, ICH guidelines, FDA and other applicable country regulations, proficiency in BASE SAS, SPSS or other statistical software, understands the sequence of running programs to ensure up-to-date data and to troubleshoot, debug programming problems and to identify data trends, and Nonverbal symbolism experience (formulas, scientific equations, graphs, musical notes, etc.,) in its most difficult phases.
