Sr. Clinical Programmer Jobs in Redwood City, California

13 jobs

Ascent Pharma is seeking a Clinical Data Associate II and a Clinical Data Manager!!! ***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 ***** Clinical Data Associate II Specific Responsibilities: This role will immediately assume study lead data management ...

Specific Responsibilities: This role will immediately assume study lead data management responsibilities for 3-5 concurrent HCV clinical trials, utilizing primarily the Medidata RAVE electronic data capture and management system. The selected candidate will manage trials in various stages, from planning, to set-up, conduct, closeout, and archiving, in high volume, while maintaining a high level o...

Performs eCRF and edit check design and ad-hoc programming support for projects assigned Works collaboratively as primary or secondary programming contact with Clinical Data Associates, Statistical Programmer, Biostatistician and other Clinical, Global Drug Safety, Regulatory and Project Management staff and vendors to meet project deliverables and timelines for clinical data acquisition, quality ...

Specific Responsibilities: . Essential Duties and Job Functions: Works collaboratively with Biostatisticians, Statistical Programmers, Clinical Research Associates, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines for statistical data analysis and reporting. Identifies potential issues in statistic...

Specific Responsibilities: . Essential Duties and Job Functions: 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 Bio...

Specific Responsibilities: . Essential Duties and Job Functions: 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 Bio...

Specific Responsibilities: Ability to immediately assume study lead data management responsibilities for 3-5 concurrent clinical trials, utilizing various electronic data capture and management systems such as Medidata RAVE or Omnicomm. Manage trials in various stages, from planning, to set-up, conduct, closeout, and archiving, in high volume, while maintaining a high level of data quality by lev...

Specific Responsibilities: . Essential Duties and Job Functions: Works collaboratively with Biostatisticians, Statistical Programmers, Clinical Research Associates, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines for statistical data analysis and reporting. Generates or oversees the production of ...

Specific Responsibilities: . Essential Duties and Job Functions: Works collaboratively with Biostatisticians, Statistical Programmers, Clinical Research Associates, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines for statistical data analysis and reporting. Generates or oversees the production of ...

Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines for statistical data analysis and reporting. Directs internal and external teams across multifunctional project or functional areas, leads initiatives to ...

Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines for statistical data analysis and reporting. Works concurrently on 3-4 assigned components of a clinical trial / project as well as other tasks as assigne...

Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines for statistical data analysis and reporting. Directs internal and external teams across multifunctional project or functional areas, leads initiatives to ...

The Senior IT Project Manager is accountable for the end to end management of very critical projects. In collaboration with appropriate clinical and business departments. The Senior Project Manager is responsible for the overall direction of mid to large scale programs with multiple sub-projects. This position works closely with SHC clinical and business leadership and leads a multi-disciplinary t...