Kodiak Sciences Inc. is seeking an experienced Clinical Programmer to support statistical programming across multiple clinical studies. The role involves writing, testing and validating SAS programs to create analysis datasets, TLFs, and other outputs for regulatory submissions and
Kodiak Sciences Inc. is a rapidly growing, clinical-stage biopharmaceutical company dedicated to transforming ophthalmology through innovative therapeutics. Our proprietary Antibody Biopolymer Conjugate Drug (ABCD) platform integrates protein engineering, polymer chemistry, small molecule drug discovery, and advanced
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives
If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We
CMM Programmer/Quality Inspect Title: CMM Programmer/Quality Inspect Position Type: Full-Time/Regular Division: NxEdge Department: Quality Location: NxEdge - Morgan Hill Job Summary & Job Duties Salary Range - $40.00 - $45.00 DOE Must have the personality and temperament to
An established industry player is seeking a Senior Manager, Statistical Programmer to join their dynamic team. This role is crucial for advancing clinical studies in Endocrinology and Oncology, where you will lead programming efforts to ensure data integrity
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON)
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives
CNC Horizontal Mill Machinist 3 As a CNC Horizontal Mill Machinist 3, you will be required to set up and run the most complex, proven, or new parts with little to no supervision. May assist programmer, department
Passionate about precision medicine and advancing the healthcare industry? Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus proprietary platform connects an entire ecosystem
Business Continuity Group Supervisor Campus: Central Services Starting Salary: $12,580.37 per month (Salary Grade: C4-79) Full Salary Range: $12,580.37 - $16,849.52 per month About the District Foothill‑De Anza Community College District is a public two‑college district
Senior Director/Director of Biostatistics Reporting to: VP, Biostatistics. Required Location: Palo Alto, CA – Three days a week onsite. Roles and Responsibilities Represent Statistics in multiple projects of cross‑functional process and standards development/improvements, and infrastructure initiatives
At Inceptive, you will help pioneer the next generation of AI-designed drugs, with the potential to positively impact billions of people, as part of a collaborative, antedisciplinary team. We advance the state of the art in
Senior Clinical Data Manager Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The companys R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS
Job Title Responsible for leading and managing the daily operations of plants in the Fremont and Livermore area and is a liaison to Quality Management in the local plants to coordinate and drive CMM Programming projects.
Clinical Data Associate - II Works collaboratively with Clinical Programmers, CRA, Statistical Programmers, Biostatisticians and other Clinical, DSPH, Regulatory and Project Management staff to meet project deliverables and timelines for clinical data acquisition, quality checking and reporting. Demonstrates a
Clinical Research Associate Candidate with academic CRO experience would also be fine, leading the study (3-4 studies). Understands data management and documentation process. Candidate who has worked on clinical trials as clinical data manager, CRF design