Biostatistician Jobs

Job Title: Biostatistician Company: General Dynamics Location: Fort Lewis, WA Description: Biostatistician Job Title BiostatisticianJob ID Number 161115Company General Dynamics Information TechnologyLocation Ft Lewis, WAJob Category Project/Program ManagementJob Description General Dynamics Information Technology is a top-tier IT integrator that provides information technology, systems engineering and professional services to customers in the defense, intelligence, homeland security, federal civil and commercial sectors. With 16,000 professionals worldwide, the company has the customer knowledge, domain expertise and proven performance to manage large-scale, mission-critical IT programs.The T2 Center researches, develops, evaluates, and deploys new and existing technologies for Psychological Health (PH) and Traumatic Brain Injury (TBI) across the Department of Defense (DoD).The Senior Biostatistician provides statistical support to psychologists working on research projects and grants in support of the T2 mission.Guidance on Proposed Research Designs: Provides specialized professional advisory services to the T2 research team. Collaborates in the preparation of proposed methodologies and statistical analyses for research projects and grants. Advises researchers on overall plans on studies and grants and related aspects of their protocols. Provides information and guidance to ensure collection of complete, accurate, unbiased and relevant data suitable for statistical evaluation. Reviews methodological plans, all project protocols, and statistical analysis sections.Expertise in the Area of data Analysis: Provides troubleshooter and consultation services when problems arise having statistical support implication. Provides statistically sound experimental design and data analysis input to meet project objectives. Generates study randomization and monitors the experimental design, sample size estimates, data summaries, final data analysis, and interpretation of results. Obtains and reviews clinical data to assure suitability for statistical summaries and analysis. Conducts/consults on statistical analyses, when indicated, and provides support for presentation and publication of research results. Keeps abreast of new developments in statistics through literature review and attendance at workshops and professional meetings. Other duties assigned.Location: This Center is located with a large medical center at Fort Lewis in Tacoma WA. T2 is the leader for the DOD in technology development efforts for behavioral health. Fort Lewis is located conveniently between the bustling metropolis of Seattle and the state capital of Olympia. The Puget Sound has 20,000 shoreline miles with bays, coves, and islands. Mount Rainier, Crystal Mountain, Snoqualmie Pass, and other nationally known winter sports areas are within 75 to 100 miles. There are more than 15 public golf courses within 20 minutes driving time, most of which are open year round. The scenic beauty of the Cascades and Olympics, the ocean, rainforests, Puget Sound and its islands, and many national and state parks are all easily accessible over excellent highways.To learn more visit www.t2health.orgRequires Doctorate degree.Requirements? Ph.D. in Statistics/Biostatistics and sound knowledge of theoretical and applied statistics.? Must have specialized experience at the level of the work of this job? Must have very strong statistical and analytic skills and knowledge of epidemiological research methods. Knowledge of advanced quantitative methods such as Multi-level analyses, Structural Equations Modeling very desirable.? Must have experience with SAS and SPSS. Familiarity with statistical software packages such as MPLUS, LISREL very desirable.? Must have effective skills in communication and team collaboration.? Must show evidence of record of scholarly publications.? Must have experience working in the social sciences.Apply Online Directly with General Dynamics Information Technology

Job Title: Senior Biostatistician Company: Regeneron Location: Tarrytown, NY Description: The statistician will serve as a statistician for one ormore study protocols. Responsibilities will include someor all of the following: contribute to study design as amember of the protocol team, develop statistical analysisplans, perform complex statistical analyses, and collaborateon final analysis and submission/manuscript preparation.Education: Doctoral or Masters degree in Statistics orBiostatistics and minimum of 3 years of related experience.Background in statistical computing within a clinicaltrial setting required including proficiency with SAS. REQUIREMENTS - QUALIFICATIONS: Senior Biostatistician Doctoral or Masters degree in Statistics or Biostatistics.- Minimum of 3 years of related experience.- Background in statistical computing within a clinical trial setting required including proficiency with SAS.EOE/M/F/D/VReneneron

Job Title: Senior Biostatistician Company: Statworks Location: Research Triangle Park, NC Description: Statworks, Inc is a high quality specialty provider of biostatistical analysis and consulting, clinical data management, and report writing services focused exclusively on clinical trials and drug development Senior BiostatisticianStatworks, Inc is a high quality specialty provider of biostatistical analysis and consulting, clinical data management, and report writing services focused exclusively on clinical trials and drug development. We are looking to grow our team of talented and experienced professionals by seeking a Senior Statistician. The Senior Biostatistician will serve as the lead for multiple statistical project activities. Provide statistical expertise, project management, and sponsor relations for specific projects involving clinical research. Responsibilities: Technical Tasks: Develop study design, protocol review/writing, and sample size calculations with customer. Develop strategy for literature review, if necessary. Review database structure and provide database management advice to customer. Oversee technical quality assurance of all data, analyses and documents. Develop analysis plans, oversee analyses, and provide interpretation of results and oversee/review generation of reports. Oversee table and listing generation. Oversee preparation and submission of major FDA, European, and Japanese regulatory documents. Develop, review, and train others on StatWorks Standard Operating Procedures. Monitor overall quality of statistical contributions. Ensure achievement of statistical deliverables while maintaining protocol objectives, StatWorks and project standards.  Administration: Mentor biostatisticians on job skills, develop training materials for associates and conduct training sessions. Assist in recruiting and hiring for staff positions. Assignment of technical support projects. Assures that orientation, scheduling of training seminars and monitoring of training check lists occurs in a timely manner. Recommends staffing and resource allocation needs.  Project Management: Participates in projects teams and Senior Statistical Reviews as Statistics Representative. Establishes and negotiates accurate timelines with internal and external customers for the completion of study related statistical activities. Participates in projecting and scheduling resources for project work. Develop and monitor budget, review monthly invoices for projects in which project management function is assigned. Perform task delegation and supervision. Maintain communications with customers, manager(s) and staff; keep them up-to-date about progress of projects, recognizing and communicating issues. Perform other project management related duties, as necessary.   Perform all other job-related duties, as necessary.  Education/ Experience Required:    M.S. or a Ph.D, in a related field, preferably mathematics, statistics or biostatistics. Minimum 8 years of experience in the clinical research field or equivalent combination of education and experience that provide the skills and knowledge necessary to perform the job. Benefits include opportunities for advancement, tuition assistance, profit sharing, 401K, flexible schedules, and competitive compensation and benefits.

Job Title: Biostatistician (216802-891) Company: Burnham Institute for Medical Research Location: La Jolla, CA Description: 216802-891 Job Description Burnham Institute for Medical Research is seeking an entry-level biostatistician/software programmer to assist scientists with statistical data analysis, data interpretation, developing research projects and programming. The successful candidate will serve as a primary point of contact and will  be responsible for determining statistically significant results utilizing sample comparisons, ANOVA, regression and correlation analysis. Additional duties include, providing training on biostatistics, assisting with writing grants, papers and preparations of data/illustrations for publications, as well as supporting a variety of bioinformatics projects.  Some projects may require programming and web development. Required Skills A Bachelors degree in Biostatistics is required, a Masters degree is preferred.  Previous experience and working knowledge of Java, Perl, MySQL, CGI, HTML, and statistical software, such as Matlab, R and/or SAS is also required.  The successful candidate will possess the ability to exercise independent judgment regarding the interpretation and optimization of data, have the ability to work independently, manage multiple projects, be a team player and have excellent verbal and written communication skills. Required Experience 1-2 years of relevant experience is a plus. Job Location La Jolla, CA, US. Position Type Full-Time/Regular Salary 40,000-60,000

Job Title: Biostatistician Company: PRA International Location: Lenexa, KS Description: Prepares and performs statistical analysis on all relevant projects for clients and PRA staff.ACCOUNTABILITIES• Designs, develops, modifies, and evaluates the technical data and infrastructure to expedite and evaluate analysis and reporting of clinical and pre-clinical studieso Provides significant input into the preparation and review of clinical study protocols and consults in the development of case report forms (CRFs)o Contributes to the design, analysis, and reporting of clinical studieso Works with the functional manager and the project manager to determine resource projections and project schedules• Performs statistical analysis and interprets resultso Prepares analysis plans and reporting specificationso Develops, modifies, and/or implements appropriate statistical techniques for the analysis of data from clinical studieso Works with programmers, writers, and clinicians to coordinate data summarization and analysis activitieso Prepares and reviews integrated statistical and clinical reports including summary statistics, graphics, tabulations, and raw data listingso Consults with other statisticians on statistical methodology, study design, and data analysiso Maintains awareness of FDA guidelines and requirements for documentation and presentation necessary for reporting of clinical trials data• Builds and maintains strategic relations with customer groupso Serves as primary functional representative on project teams; may assume the role of project managero Visits clients to discuss statistical issueso Performs billable work in accordance with PRA's policies, procedures, and SOPso Represents client regarding statistical issues at regulatory meetingso Participates in sales activities including bid defense REQUIREMENTS - QUALIFICATIONS: Biostatistician QUALIFICATIONS• Knowledge of regulatory submissions requirements for human drugs, biologics and/or devices• Knowledge of relevant to ICH statistical analysis guidelines, report writing guidelines, and regulatory submission requirements for human drugs in NA and Europe• Experience using computerized systems (PC-Windows and WORD, Excel) and relevant software (SAS)• Excellent written, oral communication and presentation skills• Read, write, and speak fluent EnglishFor Epidemiologist Only ACCOUNTABILITIES• Designs, develops, and evaluates data for benefit-risk assessments of medical devices, drugs, and biologicals during their development and post-authorization• Performs pharmaco-epidemological and statistical analyses and interprets resultso Prepares and reviews integrated summaries of safety and efficacy or other relevant regulatory submission documents including summary statistics, graphics, tabulations, and raw data listingso Serves as expert on Data Monitoring Committees (non-voting or voting members)o Supports publication generation activitieso In a senior position, effectively coaches and mentors less experienced staff membersQUALIFICATIONS• MSc degree in epidemiology, pharmaco-epidemiology, or related field required• Demonstrated expertise in areas such as drug development research, regulatory requirements, drug safety management, statistics, and therapeutic areas.PRA International

Job Title: Biostatistician Company: University of Miami Location: Miami, FL Description: We strive to deliver the best ? in patient care, research, and education. Experience amazing opportunities and outstanding rewards with the University of Miami, Miller School of Medicine. The University of Miami Miller School of Medicine, Department of Pediatrics, has an opportunity for a Biostatistician, located at the Medical Campus.  The successful candidate will be part of a collaborative and analytical research team based in the Division of Clinical Research. The is focus in this division is on clinical and translational science. S/he will work in collaboration with medical and scientific researchers under supervision from the senior staff in the Division of Pediatric Clinical Research. S/he will specialize in advanced statistical analysis, study design, development of research instruments, data collection, management and analysis, interpretation of results, preparation of reports, and preparation of manuscripts to the point of publication in peer reviewed journals. Master's degree in Statistics/Biostatistics with advanced coursework in computer science, high level analysis techniques and macro language programming; specifically SAS and SPSS. Should have specific demonstrated interest with epidemiological and medical data. The position requires one year of experience, preferably in an academic/medical center environments. We also require the ability to self-initiate and learn quickly while working with diverse projects. Experience in accessing and manipulating data from multiple data sources (e.g. relational databases, flat files, ODBC data sources, Microsoft Access) using SAS/ACCESS. Any appropriate combination of education, certifications, and/or relevant work experience will be considered.Discover all this and countless opportunities that reward your talent. The University of Miami, Miller School of Medicine is proud to offer those who lead with us competitive salaries, medical and dental benefits, tuition remission, vacation, university paid holidays and much more. The University of Miami is an Equal Opportunity/Affirmative Action Employer.

Job Title: Biostatistician Company: JDG Associates, Ltd. Location: Washington, DC Description: Opportunity BiostatisticianClient Boutique Research FirmCompensation $55,000 to $70,000Location Washington, DCEducation M.S. or equivalent degree in statistics or biostatisticsOverview Our client, a small (25 staff) yet highly-prestigious biostatistics firm, cooperates with researchers in government, industry, non-profit, and academic settings to provide statistical collaboration in the fields of clinical trials and epidemiology. They help their clients develop research programs with scientific rigor and statistical validity. Their staff of statisticians, epidemiologists, statistical programmers, and research assistants have many years of experience in clinical trials, epidemiological studies, preclinical studies, and non-clinical research. Special areas of interest include cardiovascular disease, infectious diseases, vaccine development, and cancer.Requirements - 1-4 years of statistics expertise (medical/clinical/pharmaceutical field ideal). - Strong experience in statistical analysis and SAS programming, technical writing, experience building predictive models, excellent quantitative and analytical skills - Attention to detail, accuracy, highly-motivated, self-directed, and excellent communication skills are required. - US citizenship or Permanent Residency requiredResponsibilities For clients and for work related to funded research, responsibilities include: -Statistical analyses and statistical programming. -Data analysis, including writing SAS and other statistical code. -Preparation of graphs, tables, and listings. -Database development and supervision of data entry. -Coordination of biostatistical projects under the supervision of more senior staff. -Direct liaison with clients, especially with clinic coordinators and programmers. -Preparation of reports of statistical analyses and quality control procedures. -Preparation of statistical portions of scientific manuscripts. -Calculation of sample size and power. For the scientific community at large, you will attend meetings of professional societies.

Job Title: Biostatistician Company: KENDLE INTERNATIONAL INC Location: Cincinnati, OH Description: Biostatistician Location Cincinnati, Ohio Job ID GC6449 Area of Interest Biostatistics Job Type Full-Time Regular Education Required Not Indicated Experience Required Not Applicable Relocation Provided No Travel Percentage Job Summary Developing pharmaceutical research study protocols by choosing an appropriate study design including statistical methodologies, calculating necessary sample size to achieve a pre-specified power and writing the statistical section of the protocols; generating and reviewing a statistical randomization schedules to ensure that there are no errors present and that sponsor and protocol requirements are met; writing and reviewing statistical analysis plans (SAPs) based on the protocol; reviewing and approving  listing tables specifications; providing statistical programming support; reviewing SAS annotated Case Report Forms according to SAS in a clinical environment and ICH guidelines; reviewing SAS database design and data validation plans; monitoring the progress of biostatistical clinical trial activities; performing checks on statistical data for adherence to protocol; performing statistical analysis and preparing corresponding sections of the research reports; and writing and reviewing statistical reports and clinical study reports. Core Responsibilities Master’s Degree or foreign degree equivalent in Statistics or Biostatistics and one year’s experience in the job offered or one year’s experience as a Research Assistant. Special requirements – Experience using SAS in clinical environment and ICH guidelines Skills & Attributes Any Applicant who is interested in this position may apply by regular mail to: Ms. Casey Buchanan Kendle International, Inc. 500 Carew Tower 441 Vine Street Cincinnati, OH 45202 Kendle is an Equal Opportunity Employer.

Job Title: Biostatistician II - Department of Biostatistics Company: Vanderbilt University Location: Nashville, TN Description: This position will apply a variety of intermediate and advanced statistical techniques and technical skills independently and/or as a member of a research team to promote the collection, analysis and interpretation of data arising from research studies in an academic research program. Minimum Requirements: This position requires a Master’s degree in Biostatistics, Statistics, Mathematics, or other highly quantitative field with excellent command of one of the following computing languages: R, Stata, or SAS. Preferred computing languages are R or Stata. Experience is preferred in at least one other language from the following: R, Stata, SQL, Perl, Python, Ruby, C/C++, or SAS Training in biology or biomedical research is preferred. Excellent written and oral communication skills are necessary Training or significant experience in 5 of the following statistical areas is needed: Experimental or Study Design Multiple Regression Longitudinal Data Analysis Survival Analysis Logistic Regression Categorical Data Analysis Clinical Trials Methodology Bayesian Methods Machine Learning/Bioinformatics Additional Information: This is a Full-Time position (40 hours per week). Shift hours are 8:00am - 5:00pm; Monday thru Friday. Salary ranges from $3,816 to $6,914 monthly; dependent upon years of education and experience. Background screens will be performed and education will be verified prior to employment. Please be prepared to provide required information and/or documentation. Vanderbilt is a smoke-free workplace in compliance with the Non-Smoker Protection Act, Tennessee Code Annotated 39-17-1801-1810. In accordance with that law and Vanderbilt policy, smoking is prohibited in all enclosed areas on Vanderbilt property.

Job Title: Senior Biostatistician Company: Adecco Location: Bedminster, NJ Description: Senior Biostatistician Location: Bedminster, NJ Category: Medical & Science Status: Temporary/Contract Reference: US_EN_ Register to View 93 Salary: N/A Posted: September 25,2009 Adecco Engineering and Technical, a division of the world leader in the recruitment of scientific and engineering professionals, has an immediate opening for a Senior biostatistics for a 6 month + contract position in Bedminster, NJ. Job Duties: The position participates in planning and execution of statistical tasks for assigned studies, including preparation and maintenance of the Analysis Plan (AP), and ensuring the quality controlled production of all tables, listing and graphs for the clinical document while adhering to the pre-specified analyses and timelines. The position may serve on departmental teams and make recommendations for departmental standards. Essential: Statistical expertise in at lease of of the following Design - crossover, multiplicity, interim analyses, non-inferiority, sample size and/or power. Analysis - treatment by center interaction, multi-center, missing value imputation, covariate, and/or subpopulations. Methodology - analysis of variance and mixed linear models, survival analysis, categorical data analysis, reliability, multivariate analysis, robust estimation, nonparametric techniques, and/or group dequential analyses. Working knowledge of SAS, excellent oral and written communications skills. Flexible and well organized with the initiative to take on unfamiliar tasks and work well under pressure. Education: MS or above in statistics or equivalent with at least two years industry working experience. If you are interested in this opportunity or other opportunities available through Adecco Engineering and Technical, email Tom Powell directly at Register to View The Adecco Group is a Fortune Global 500 company and the global leader in HR services. Our group connects over 700,000 associates with our business clients each day through our 6,600 offices in over 70 countries and territories around the world. We offer employment opportunities at any stage in your professional career. Contact us today to discuss available contract and direct hire positions. Adecco Engineering and Technical is an Equal Opportunity Employer. Tom Powell 10 PARSONAGE RD., SUITE 200 Not Specified Register to View Technical support Privacy policy Terms of use USA Office locator Adecco Worldwide