Clinical trials Jobs in California

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Statistical Programmer (Clinical Trials)

Ledgent Technology

Remote

Contract

We are seeking a Statistical Programmer to work on a remote team for a project with our client. The preferred R stack experience includes dplyr, rmarkdown, dbplyr, ggplot2, roxygen, and plotly to solve complex challenge. We are unable to work with 3rd party candidates. Summary The main function of Sr. Analyst is to develop, validate datasets, tables/listing/figures using SAS/R programming language, and other ad-hoc request to support business requirements. Job Responsibilities *In this rol

Sr. Principal Statistics

PARAKEET WORLD SOLUTIONS LLC

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

eClinical Project Manager

Biogensys

Remote

Contract

Title: eClinical Project Manager Duration: Long term Contract Location: NJ/NY- Remote option available Rate: Flexible Required skills: Proven experience managing eClinical or eCOA product implementations.Own the end-to-end delivery of eClinical initiatives, including eCOA platform rollouts, device provisioning, and integration with client systemsFamiliarity with device provisioning workflows and mobile device managementStrong understanding of clinical trial operations, regulatory compliance, and

Clinical Research Associate

Zachary Piper Solutions, LLC

Sacramento, California, USA

Full-time

Piper Companies is currently seeking an Oncology Clinical Research Associate (CRA) for an opportunity in Sacramento, California (CA). The Oncology Clinical Research Associate (CRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization. Responsibilities for the Oncology Clinical Research Associate: Conduct site and study visits and perform all site monitoring activities across multiple study Responsible for both remote and on-site monito

Senior Sourcing Manager*

Cube Hub, Inc.

California, USA

Contract

Description: True Job Title: R&D Sourcing Manager Location: Prefer Foster City, but can be remote in the US The R&D Sourcing Manager will be responsible for sourcing and contracting development organizations to support client global Phase I IV clinical trials, as well as other ad hoc projects within the Vendor Outsourcing department. This role will primarily focus on clinical ancillary services and systems used across development. Familiarity with technology, systems, and software is a plus,

Development Engineer 3

Katalyst Healthcares and Lifesciences

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

Clinical Research Associate

Zachary Piper Solutions, LLC

Los Angeles, California, USA

Full-time

Piper Companies is currently seeking a Clinical Research Associate (CRA) for an opportunity in Los Angeles, California (CA). The Clinical Research Associate (CRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization. Responsibilities for the Clinical Research Associate: Conduct site and study visits and perform all site monitoring activities across multiple study Responsible for both remote and on-site monitoring and study activation

SAS Programmer

Katalyst Healthcares and Lifesciences

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.

SCI CTO Trial Activation Specialist (Hybrid)

Stanford University

Remote or Stanford, California, USA

Full-time

Stanford Cancer Institute - Clinical Trials Office Research Services Trial Activation Lead - Hybrid Position The Stanford Cancer Institute (SCI) is one of an elite number of National Cancer Institute-Designated Comprehensive Cancer Centers in the country, and is a prominent, dynamic, growing and complex Institute within the Stanford University School of Medicine. The SCI actively works to build synergies and collaborations among faculty with cancer-relevant expertise from four Schools and over

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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

Global IT Compliance Sr Specialist

Thermo Fisher Scientific

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

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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

Associate Director, Data Monitoring Committee (DMC) Expert

Eli Lilly and Company

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

Associate Director, Biotherapeutic Engineering & Bioconjugation

Novartis

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.

Associate Director - Hematology, Oncology Data Sciences & Digital Health

Johnson & Johnson

Remote or New Brunswick, New Jersey, 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

Senior Manager Data Management

Katalyst Healthcares and Lifesciences

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.

Analyst, External Data Acquisition Expert

Johnson & Johnson

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

Manager Master Data Lead

Johnson & Johnson

Remote or Horsham, 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

Senior AI/ML Software Engineer - Remote

UnitedHealth Group

Remote or Eden Prairie, Minnesota, USA

Full-time

Optum is a global organization that delivers care, aided by technology to help millions of people live healthier lives. The work you do with our team will directly improve health outcomes by connecting people with the care, pharmacy benefits, data and resources they need to feel their best. Here, you will find talented peers, comprehensive benefits and career development opportunities. Come make an impact on the communities we serve as you help us advance health equity on a global scale. Join us

Clinical Data Analytics Leader

Software Guidance & Assistance

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