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POSITION SUMMARY: This position is accountable for specification, production and validation of SDTM datasets through the life of a clinical trial and in preparation for submission to regulatory agencies. This position is charged with further development of a clinical SAS programming team in general: recruiting, hiring, and training, mentoring and managing a staff of highly technical SAS programme...

About The Opportunity:The Associate Director of Statistical Programming provides guidance on statistical programming to a team of about 10 in-house programmers. The AD will collaborate with leaders of other therapeutic areas and database programming area to identify and establish global programming and database standards. Our client has a variety of products on the market and an advancing pipelin...

We are seeking a Manager (or Sr. Manager) of Statistical Programming.Must work onsite in Princeton, NJ.Select candidates will be able to work from home 2 to 3 days per week after established.Relocation assistance available.Responsibilities include:• Supervision of less-experienced statistical programmers within project activities.• Statistical Programming lead for large global or other major progr...

About The Opportunity:The Associate Director of Statistical Programming provides guidance on statistical programming to a team of about 10 in-house programmers. The AD will collaborate with leaders of other therapeutic areas and database programming area to identify and establish global programming and database standards. Our client has a variety of products on the market and an advancing pipelin...

Duties: Candidate should be able to perform programming activities across several trials with a given compound including publication and regulatory submission activities. Develop programming specifications for analysis dtasets, pooled, datasets and deliverables in consultation with the statistician.Review and provide feedback on statistical analysis plan, output shells, CRF, edit checks and other ...

* This is a permanent/salaried role (not a contract)* This position is remote/work from home.*A PhD is required.RESPONSIBILITIES: - Coordinate statistical reporting activities for multiple projects simultaneously. - Develop and review statistical analysis plans based on study specific documents and sound statistical methodology. - Develop, maintain, and produce statistical programs and specific...

Senior Statistical Programmer Primary Job Functions: Develops and tests SAS Software programs to complete complex Biostatistical analyses identified in statistical analysis plans with no supervision. Develops, tests, and validates complex Tables Listings, and Graphs for specific projects and project shells in the Global Biostatistics Department. Develops and tests SAS Software programs to comp...

At least 5 years of pharmaceutical experience at Ph.D. level (or 8 years at MS level ) in biostatistics, statistics • Excellent communication skills (verbal and written) • Good team player • Advanced level in SAS but not looking for a SAS programmer. Looking for a senior level statistician who is advanced in SAS programming. Additional Skills: • Extensive experiences in phase III trials, in p...

Principal Statistical Programmer Primary Job Functions: Develops and tests SAS Software programs to complete complex Biostatistical analyses identified in statistical analysis plans with no supervision. Develops, tests, and validates complex Tables Listings, and Graphs for specific projects and project shells in the Global Biostatistics Department. Develops and tests SAS Software programs to c...

BiostatisticianREQUIREMENTSM.S./Ph.D. in Statistics/Biostatistics or equivalent discipline 5-10 years experience in the analysis of clinical data Proficient in SAS KEY SKILLS & BEHAVIORS Work extensively with Biometrics project team members. Interact with other members of Company project team. Respond to questions from clients. Effectively communicate data findings to the data manager and r...

Acts as lead statistical programmer for a project. -May participate in sub-team meetings as a representative of Statistical Programming group. -Provides consistency and quality assurance across various studies. -Independently identifies issues in the analysis plan from previous experience and knowledge. -Collaborates with Biostatisticians and Clinical Research Scientists on studies and helps d...

Works collaboratively with Clinical Development staff to meet project deliverables and timelines for statistical data analysis and reporting. Assesses the quality and consistency of analysis data and performs cross-study analyses. Uses internal macros or writes SAS® macros to automate study deliverables. Works as a primary programmer for multiple Phase 1-4 studies. Assists in submissions of el...

*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...

The selected candidate will be responsible for the following: Review of shell data displays for consistency and to ensure that all CRF fields are displayed on listings. Ensuring overall consistency of a project including macro definitions, debugging programs, and documentation. Programming of customized data displays in accordance with approved statistical analysis plan and shell displays for c...

Johnson & Johnson companies are equal opportunity employers. Immunology Specialist Academic – Dallas, TX - Janssen Biotech, Inc.-0589150825 Description Janssen Biotech, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for an Immunology Specialist Academic for the Dallas, TX territory, to include Houston, Temple and San Antonio. For more than 30 years, Janssen Biotech, I...

SAS Experience in Pharmaceutical or equivalent: 7 years. Oncology experience preferred. * Experience with applying censoring rules and deriving PFS, OS and other time to event variables needed.* Have good knowledge of statistical terminology, clinical data structure, clinical tests, medical terminology, regulatory standards and protocol designs.* Strong SAS programming / Macros development / SAS ...

Full-time Opportunity for a Senior SAS Programmer.Education: Masters (US) in statistics or a related science Professional/Technical Skills & Experience Experience of extracting, manipulating, summarizing, analyzing and presenting data using SAS procedures Experience of SAS/MACRO, SQL and SAS/BASE procedures Experienced in use of SAS/GRAPH and Statistical procedures Experience ...

Experience in generating mapping specifications, developing/delivering CDISC compliance SDTM datasets along with annotating CRFs for ongoing/legacy studies across various therapeutic areas. Develop macros to create SDTM datasets along with standard programs to generate Define.xml for regulatory submissions. ·Extraction of data for reporting and generating other databases from SAS databases on mul...

Experience in generating mapping specifications, developing/delivering CDISC compliance SDTM datasets along with annotating CRFs for ongoing/legacy studies across various therapeutic areas. Develop macros to create SDTM datasets along with standard programs to generate Define.xml for regulatory submissions. ·Extraction of data for reporting and generating other databases from SAS databases on mul...

Are you looking for a new and exciting opportunity? Do you have experience in the pharmaceutical industry with clinical trials & project management experience?Well this Expert Clinical Manager position in East Hanover, NJ maybe the position for you. Responsible for all operational aspects of 1 or more OGD clinical trial(s) under the leadership of Clinical Trial Head (CTH). Support all scientific ...