clinical trials Jobs in california

1 - 20 of 79 Jobs

Python Developer - (clinical data)Job Title - Python Developer - (clinical data)

Radiant System, IncCompany Name - Radiant System, Inc

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Remote

Contract

Seeking a Python Developer with strong experience in clinical data standards (SDTM/CDISC) and a background in the pharmaceutical industry. Role involves developing automation pipelines and AI/ML models to transform clinical trial data into SDTM-compliant datasets. Must-Haves: 8+ years in pharma/clinical domain 3+ years Python development SDTM, CDISC, ADaM, raw datasets Experience with AI/ML (NLP, classification) Tools: Pinnacle 21, Define.xml Nice-to-Have: Metadata-driven automation Knowledge of

Sr. Regulatory affairs Consultant-W2 ONLYJob Title - Sr. Regulatory affairs Consultant-W2 ONLY

VetForce SolutionsCompany Name - VetForce Solutions

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Remote

Contract

Sr. Regulatory affairs Our client is a rapidly expanding biotech company based in China that recently partnered with a major pharmaceutical company for research collaboration efforts, in hopes of discovering and developing novel oral drug candidates across multiple therapeutic indications (oncology, immunology, etc.) Our client is looking to bring on a Senior Regulatory Affairs Consultant (Senior/Director Level), who will provide strategic regulatory guidance as the client navigates the regulato

Senior BiostatisticianJob Title - Senior Biostatistician

Radiant System, IncCompany Name - Radiant System, Inc

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Remote

Contract

Role: Contribute with your statistical expertise to the design and analysis of one or more clinical trials or the clinical development plan of one compound/program.Will closely collaborate with program partners and stakeholders to deliver on the statistical deliverables for one or more clinical trials and contribute to HA submissionsWill report to a franchise team leader, within the Biostatistics and Statistical Modelling organisationWill carry out functional responsibilities in accordance with

Sr. Principal StatisticsJob Title - Sr. Principal Statistics

PARAKEET WORLD SOLUTIONS LLCCompany Name - PARAKEET WORLD SOLUTIONS LLC

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Remote

Contract

Job Title: Sr. Principal StatisticsLocation: Remote Duration: 6 MonthsEmployment Type: W2 ContractExperience Level: Mid-SeniorEducation Required: Ph.D. or MS in Statistics or BiostatisticsIndustry: Pharmaceuticals Job Summary:The Sr. Principal Statistician will lead statistical activities in clinical trials, from protocol development to final study reporting. The role will also contribute to regulatory filings, in-licensing evaluations, and marketing support. Key Responsibilities:Review protocol

Global IT Compliance Sr SpecialistJob Title - Global IT Compliance Sr Specialist

Thermo Fisher ScientificCompany Name - Thermo Fisher Scientific

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Pennsylvania, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing so

Principal, Electronic Data Capture DeveloperJob Title - Principal, Electronic Data Capture Developer

Takeda pharmaceuticalCompany Name - Takeda pharmaceutical

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Massachusetts, USA

Full-time

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Princip

Analyst, External Data Acquisition ExpertJob Title - Analyst, External Data Acquisition Expert

Johnson & JohnsonCompany Name - Johnson & Johnson

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Remote or Pennsylvania, USA

Full-time

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m

Associate Director - Hematology, Oncology Data Sciences & Digital HealthJob Title - Associate Director - Hematology, Oncology Data Sciences & Digital Health

Johnson & JohnsonCompany Name - Johnson & Johnson

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Remote or New Brunswick, New Jersey, USA

Full-time

Associate Director, Biotherapeutic Engineering & BioconjugationJob Title - Associate Director, Biotherapeutic Engineering & Bioconjugation

NovartisCompany Name - Novartis

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San Diego, California, USA

Full-time

Job Description Summary As Associate Director of Biotherapeutic Engineering & Bioconjugation, you will have an opportunity to join the Biologics Research Center (BRC) as a leader at the cutting edge of discovery and development of innovative medicines to address unmet medical needs. BRC builds the biologics pipeline in collaboration with Biomedical Research (NBR) Disease Areas and Platforms via a breadth of technologies for discovery of antibody, protein, gene therapy and RNA-based therapeutics.

Development Engineer 3Job Title - Development Engineer 3

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Santa Clara, California, USA

Full-time

Job Description: The Medical Imaging Specialist is responsible for providing CT and MR imaging expertise for the Intuitive 3D modelling service and operation team. This includes performing initial inspection of CT and MR scans received for 3D model segmentation, providing in-process consultation for segmentation technicians, and performing final QC for segmented 3D models to ensure delivery of high-quality 3D models to customers for use in patient education, pre-operative planning and intra-ope

SAS ProgrammerJob Title - SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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San Diego, California, USA

Full-time

Responsibilities: Serves as lead programmer for assigned projects to provide statistical and programming support in one or more Phase I- clinical studies. Design and perform quality checks on analysis datasets, tables, listings, figures (TFL), and written reports to support clinical trial results using SAS. Create and review annotated CRF to STDM datasets. Produce and maintain technical programming specification documents. Lead and actively participate in client and project review meetings.

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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South San Francisco, California, USA

Full-time

Responsibilities: Performs all SAS programming required for clinical trial analysis and reporting. Ensures that activities and processes performed are conducted according to sponsor requirements. Works closely with the Biostatistics and Data Management departments on various clinical projects. Designs and/or reviews database structure. Writes edit checks from the Data Cleaning Plan (DCP) specifications. Creates derived-analysis datasets. Executes analyses specified in the Statistical Anal

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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San Diego, California, USA

Full-time

Responsibilities: Manage programming activities on project or study level, including managing CROs to ensure deliverables are accurate and compliant. Act as a Programming SME for assigned studies, including authoring/reviewing programming specifications, such as SDTM/ADaM specifications, TFLs creation and QC for reporting events, ESUB packages, and documenting production and validation programs. Apply programming skills to support statistical analysis, clinical reporting, regulatory submission

Senior Manager Data ManagementJob Title - Senior Manager Data Management

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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San Diego, California, USA

Full-time

Responsibilities: Responsible for data management documentation, including, but not limited to data management plan(DMP), CRF, eCRF design, edit check specifications, data issue logs, and data review plans and ensures all documents follow study design and regulatory requirements. Maintain Data Management outsourcing metrics and key performance indicators to aid the selection of CRO partners / Vendors and the ongoing management of partnerships. Participate in vendor qualifications and audits.

Clinical Data Analytics LeaderJob Title - Clinical Data Analytics Leader

Software Guidance & AssistanceCompany Name - Software Guidance & Assistance

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South San Francisco, California, USA

Contract

Software Guidance & Assistance, Inc., (SGA), is searching for a Clinical Data Analytics Leader for a direct placement assignment with one of our premier Pharmaceutical Services clients in South San Francisco, CA. Responsibilities : The Data Analytics Leader (DAL) in Early Clinical Development (ECD) Data Intelligence team supports ECD study teams by delivering timely and high-quality analysis and real-time interactive visualizations. The DAL is an expert in data analysis and data insights, enabl

Computer System Validation Analyst - R Studio & Clinical SystemsJob Title - Computer System Validation Analyst - R Studio & Clinical Systems

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Remote or New Jersey, USA

Full-time

Responsibilities: Lead validation planning, risk assessment, and execution for R Studio, GitLab, and Medidata Rave EDC. Develop and execute validation documentation including: Validation Plans (VP.). User Requirements Specifications (URS.). Risk Assessments (RA.). Functional and Design Specifications. Traceability Matrix (RTM.). Test Protocols (IQ/OQ/PQ or CSA-based scripts.). Validation Summary Reports (VSR.). Collaborate with cross-functional stakeholders including Clinical Data Mana

Sr. Data Engineer with Medical ImagingJob Title - Sr. Data Engineer with Medical Imaging

ADDSOURCECompany Name - ADDSOURCE

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San Francisco, California, USA

Third Party

Title: Sr. Data Engineer with Medical Imaging Location: San Francisco, CA (4 days onsite every week) This position is for a Sr Data engineer to join this global team of Imaging data managers to realize the product vision and value Mandatory Skills: Medical Imaging, Data engineering, Python Key Responsibilities: Imaging Data Pipeline delivery : Design, implement and maintain automated pipelines for onboarding, verifying, transforming and curating biomedical imaging data from clinical trials and

Analyst II, External Data Acquisition ExpertJob Title - Analyst II, External Data Acquisition Expert

Johnson & JohnsonCompany Name - Johnson & Johnson

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Remote or Pennsylvania, USA

Full-time

Programmer Analyst IIJob Title - Programmer Analyst II

University of Southern CaliforniaCompany Name - University of Southern California

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San Diego, California, USA

Full-time

Location: San Diego, CA Schedule: Hybrid (3 days per week in the office) The Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California is an academic institute comprised of an expert group of scientific collaborators committed to advancing the development of new treatments for Alzheimer's Disease (AD) through innovative clinical trials. We are seeking a Programmer Analyst II to join our growing team. This role is ideal for a motivated develop

Sr. Staff Software Engineer - AI Products and PlatformsJob Title - Sr. Staff Software Engineer - AI Products and Platforms

Eli Lilly and CompanyCompany Name - Eli Lilly and Company

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Remote or Indianapolis, Indiana, USA

Full-time

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined