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Biotech Programmer Jobs

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ead Statistical ProgrammerDynamic and industry-leading CRO in Cary, NC is seeking an established Lead Statistical Programmer to join their in-office team on either permanent (or long-term contract) basis. SUMMARY OF POSITION: Provide Lead Statistical Programming support in the project specific programming of statistical tables, listings, figures, and analysis data sets for clinical trials and/or...
Ascent Pharma is hiring a Contract Statistical Programmer to be located near SSF, CA orLos Angeles, CA! ***APPLY TODAY OR REFER A FRIEND! We offer a terrific referral bonus! Divna Rosenzweig/Sr. Clinical Development Recruiter (310) 933-4549 Please send resumes directly to ***** QUALIFICATIONS Degree in statistics preferred (or math, and 2 courses in stats or a certificate ...
*This position is work from home/remote.Clinical Programmer General Description: Plan and coordinate database design, development, implementation, maintenance, and user support of clinical systems. Provide technical expertise in conjunction with internal and external clients. Program, test, and document databases in accordance with programming standards and validation procedures. Program data...
Work experience in Medical Affair and Oncology Studies are preferred.Responsibilities will include, but are not limited to:? Develop, program, test and maintain clinical trial databases and data entry screens using Oracle Clinical or Central Designer in accordance with company standards? Review computer validation/edit checks for in-house and outsourced studies? Develop, program, test and maintain...
Lead Statistical ProgrammerDynamic and industry-leading CRO in Cary, NC is seeking an established Lead Statistical Programmer to join their in-office team on either permanent (or long-term contract) basis. SUMMARY OF POSITION: Provide Lead Statistical Programming support in the project specific programming of statistical tables, listings, figures, and analysis data sets for clinical trials and/o...
Senior Statistical Programmer Dynamic and industry-leading CRO in Cary, NC is seeking an established Statistical Programmer to join their in-office team on either permanent (or long-term contract) basis. SUMMARY OF POSITION: Provide senior-level Statistical Programming support in the project specific programming of statistical tables, listings, figures, and analysis data sets for clinical trial...
5 Years experience as a Statistical/SAS Programmer Industry experience required - Serves as lead Statistical Programmer to achieve milestones on one or more studies.- Develops and implements Statistical Programming Specifications and QC plans with lead statistician for one or more studies.- Works closely with study team to assure quality data and deliverables.- Provide resource estimates, timeli...
Ascent Pharma is hiring a Contract Statistical Programmer to be located near SSF, CA orLos Angeles, CA! ***APPLY TODAY OR REFER A FRIEND! We offer a terrific referral bonus! Divna Rosenzweig/Sr. Clinical Development Recruiter (310) 933-4549 Please send resumes directly to ***** QUALIFICATIONS Degree in statistics preferred (or math, and 2 courses in stats or a certificate ...
Clinical Programming Analyst Clinical Programming Analysts are needed to take on a senior role for this global CRO and their ongoing cardiovascular, oncology and virology studies. This company is nationally recognized as an amazing place to work for, since they encourage professional success as well as personal growth. The benefits are highly competitive and suit professionals looking to take on ...
·Extraction of data for reporting and generating other databases from SAS databases on multiple platforms. ·Written specifications of data reports using various software ·Create timelines, time estimates, SAS programs and supporting documentation.·Work on CDISC compliant studies as well as client specification studies. ·Annotate CRF’s and create SDTM DATASETS, ADaM DATASETS ·Create special rep...
Contribute to computer programming efforts for a clinical trial drug project and to provide programming support for clinical trial data reporting and regulatory submissions. Assumes protocol level and some project management responsibility while supporting the Programming and Statistics lead. Able to support multiple protocols independently and to contribute to integrated summaries of efficacy and...
Sr. Clinical SAS Programmer: Contribute to computer programming efforts for a clinical trial drug project and to provide programming support for clinical trial data reporting and regulatory submissions. Assumes protocol level and some project management responsibility while supporting the Programming and Statistics lead. Able to support multiple protocols independently and to contribute to integr...
CDISC Standards SME The standards SME will work in the biometrics and data solutions group. This role will be responsible to ensure compliance and consistent adoption of the clinical data standards in data representation, reporting and regulatory submission process. Primary focus of this role will be on compliance and adoption of CDISC based data models and standards. This includes the SDTM, ADaM...
Statistical Programming ConsultantExpectations: •Minimum of 5 years clinical/statistical programming experience within clinical development including supporting minor regulatory filings (e.g. sNDAs, Investigator Brochures (IB), Development Safety Update Report (DSUR)). Looking for stability in assignments. •Demonstrated knowledge of drug development process, particularly clinical development, an...
Masters-Level Statistical Analyst: Industry-leading, therapeutically-focused Contract Research Organization is seeking multiple, top-tier Masters-level Statistical Analyststo join their Cincinnati HQ. DESCRIPTION OF JOB DUTIES: Write statistical programs for use in creating analysis datasets, tables, listings, and figures; Review analysis plans for appropriate methods; Program study analyses ...
About The Opportunity: Our client has a variety of products on the market and an advancing pipeline of promising candidates. Our mid-sized pharmaceutical client focuses in areas of Oncology, Respiratory Disease, Inflammation, Cardio, Gastro, and Neuroscience. This Is Your Day To Day: - Provides critical clinical programming support to projects. - Interacts directly and independently with Biost...
About The Opportunity: Our client has a variety of products on the market and an advancing pipeline of promising candidates. Our mid-sized pharmaceutical client focuses in areas of Oncology, Respiratory Disease, Inflammation, Cardio, Gastro, and Neuroscience. This Is Your Day To Day: - Provides critical clinical programming support to projects. - Interacts directly and independently with Biost...
About The Opportunity: Our client is seeking a Principal Statistical Programmer to support Biometrics project needs.In this role, the Principal SAS Programmer will serve as a lead programmer for projects; interact with various programming aspects of clinical studies; and manage Biometrics teams for projects. Our client is a leading mid-sized provider of comprehensive clinical research and develo...
About the Opportunity: Our client is a leading provider of pharmaceutical support services, partnering with life science companies to make medicine and medical products safer and more accessible. Their diverse suite of services helps bridge the gap between development and delivery and builds brand loyalty through patient access and adherence.This Is Your Day To Day: - Perform project-related pro...
ESSENTIAL DUTIES AND RESPONSIBILITIES: ? Gathers programming requirement, prepares documents and tests required programs. ? Designs and populates the analysis datasets, creates tabulations and listings from clinical trial data. ? Develops / maintains SAS programming structure and archival system. ? Designs and delivers clinical reports as requested. Tracks requests of clinical reports and ensu...