Clinical Trials jobs in California

Los Angeles, California

•

Today

Software Guidance & Assistance, Inc., (SGA), is searching for an Sr. Project Manager for a Contract assignment with one of our premier Healthcare clients working remote PST hours. Responsibilities : The Senior Project Manager (Sr. PM) of the Clinical Trials Development (CTD) Team will participate in all Investigator Initiated Trial (IIT) research activities as part of the clinical research team within the Department of Medicine, Division of Hematology Oncology at the firm. Working under t

Contract

USD 50.00 - 65.00 per hour

US_Software Engineer II_CO

South San Francisco, California

•

Today

Job Title: Software Engineer II Job Location: San Francisco California 94080 Job Duration: 12 months with possible ext Position Summary Early Development (gRED), within Early Clinical Development Informatics (ECDi), is seeking an experienced Software Engineer to design, develop, and optimize tools and platforms that accelerate clinical trial development and help bring life-changing medicines to patients faster. In this role, you'll work with engineers, analysts, and business stakeholders to t

Easy Apply

Contract

$76 - $76.51

Senior Biomedical Engineer

Oakland, California

•

Today

Location: Oakland, CA Salary: $125,000.00 USD Annually - $150,000.00 USD Annually Description: Senior Biomedical Engineer Location: Oakland, CA - Hybrid Compensation: $130,000-$150,000 annually About the Opportunity A privately held medical device company developing innovative treatments for venous disease and lymphedema is seeking a Senior Biomedical Engineer to join its R&D organization. This is a highly hands-on senior technical contributor role focused on the development of catheter-ba

Contract

USD 125,000.00 - 150,000.00 per year

Project Manager/ Business Analyst (Clinical Operations)

Hybrid in Foster City, California

•

2d ago

Job Title: Project Manager/ Business Analyst (Clinical Operations) Location: Foster City, CA (Hybrid)Employment Type: Full-Time (FTE) Job SummarySeeking a Senior Project Manager / Business Analyst with strong Clinical Operations expertise and hands-on experience in Risk-Based Monitoring (RBM/RBQM). Responsible for requirements gathering, project delivery, stakeholder management, and implementation of clinical systems and monitoring processes. Key ResponsibilitiesLead requirements gathering for R

Easy Apply

Full-time

$160,000 - $160,000

Veeva Vault Configurator Clinical Suite

Remote

•

Today

Solution IT Inc. is looking for Veeva Vault Configurator Clinical Suite for one of its clients in Remote Job Title: Veeva Vault Configurator Clinical Suite Veeva Vault Configuration & Enhancements Configure and maintain Veeva Vault R&D applications (e.g., Vault Clinical, Vault RIM, Vault Quality, Vault Safety, or related modules). Develop and maintain objects, fields, lifecycles, workflows, roles, picklists, document types, and other Vault components. Execute configuration deployments, manage

Easy Apply

Contract, Third Party

Clinical Trial Lead

Remote or Warsaw, Indiana

•

Today

Kelly Science and Clinical FSP is currently seeking a Clinical Trial Lead for a long-term engagement in Raynham, MA, West Chester, PA, Palm Beach Gardens, FL, or Warsaw, IN with one of our Global clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a vari

Easy Apply

Full-time

Clinical Trial Product Owner

Remote

•

7d ago

We are hiring for a Product Owner. It s a long-term contract role // Fully Remote role. Title : Product Owner Work Schedule: Fully Remote role. Required Skills : Product Owner with Pharma or Clinical Trial Platform Please email me your resume at Role Overview The Product Owner for the Clinical Trial Platform is responsible for defining the product vision, strategy, and roadmap for technology that supports end to end clinical trial execution. This role blends product owner discipline with deep

Easy Apply

Full-time

Depends on Experience

Senior Clinical Research Associate

Remote

•

Today

100% TRAVEL ROLE EST Candidates will have to travel sites located in Eastern Time zone. CST Candidates will have to travel sites located in Central Time zone. West Coast Candidates will have to travel sites located in West Coast Time zone. Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (Google Cloud Platform) and International Conference on Harmonization

Easy Apply

Contract

$70 - $80

Senior Manager - Research and Development Accounting

Remote

•

Today

Description: Remote Our client seeks a contract Research and Accounting Lead to own the monthly close for R&D activities in accordance with U.S. GAAP and internal policies. The role will drive accruals, support accurate period recognition, and partner with Clinical Operations, Clinical Development, CMC, Program Management, FP&A, and external vendors. The position will prepare analyses and schedules that inform monthly, quarterly, and annual close and support financial reporting requirements.

Full-time

Clinical Services Project Manager I

Remote

•

Today

Job Title: Clinical Service Project Manager Job Location: Orro Valley, AZ 85755 Job Duration: 12 months with possible ext Job Summary Manages low- to medium-complexity clinical and lab services projects from initiation to completion, ensuring delivery on time, within budget, and in compliance with pharma services plans. Acts as the primary point of contact for Pharma and Roche clients. Key Responsibilities Project Management: Oversee multiple clinical testing and lab services projects, esta

Easy Apply

Contract

Regulatory Affairs Specialist Small Molecule

Remote

•

Yesterday

Job Title: Clinical Regulatory Affairs Specialist Small Molecule Location: Remote We are seeking a Clinical Regulatory Affairs Specialist with 9+ years of experience supporting small molecule clinical development programs.Key Requirements:Strong experience in Clinical Regulatory AffairsHands-on experience with Veeva Vault TMF or similar.Experience with IND, CTA, and NDA submissionsKnowledge of ICH-Google Cloud Platform, FDA, EMA, and global regulatory requirementsExperience supporting clinical

Easy Apply

Contract, Third Party

Depends on Experience

Associate Director - External Data Acquisition Lead (EDAL)

Remote

•

Today

At Genmab, we are dedicated to building extra[not]ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees. Our people are compassionate,

Full-time

USD 157,360.00 - 236,040.00 per year

Snowflake Administrator, Clinical Healthcare

Remote

•

8d ago

Job Title: Snowflake Administrator, Clinical Healthcare Location: Remote USA Position: Contract 6-months + Join a Leading Healthcare Organization! TalentFish is casting a line for a Snowflake Administrator to support a large healthcare system implementing a Snowflake enterprise data platform. Overview The Snowflake Administrator will be responsible for Snowflake administration, platform configuration, performance tuning, security, and integration with Informatica and Epic healthcare data syst

Easy Apply

Contract

$65 - $80

Clinical Project Manager with BA background

Hybrid in Foster City, California

•

2d ago

Role SummaryWe are seeking a Senior Project Manager / Business Analyst with deep Clinical Operations expertise and handson experience in RiskBased Monitoring (RBM/RBQM) initiatives. This role combines strong business analysis capabilities with program/project management ownership, supporting enterprisescale clinical systems and processes.The ideal candidate will independently manage stakeholder engagement, requirements definition, delivery coordination, and governance for RBM initiatives, workin

Easy Apply

Full-time

Depends on Experience

Lead AI Engineer with Spark, AWS Services

Remote

•

Today

We're looking for a Lead AI Engineer skilled in Spark and AWS Services to become part of the RBQM Production Pod within the program. In this position, you'll construct and sustain data pipelines that drive AI/GenAI applications supporting Risk-Based Quality Management for clinical trials. The primary focus of this role includes RAG document ingestion, vector indexing, and developing data APIs for AI applications. Responsibilities Architect and construct RAG document ingestion pipelines (chunking

Full-time

User Study Proctor

Cupertino, California

•

7d ago

Objective/ Engagement Overview - User Study Proctors We are looking for user study proctors to complete data collection for ongoing foundational research informing product design in the Audio and Vision space. Skills User study proctors Excellent communication skills Organized Work exceptionally well in a fast-paced environment Able to multitask between tasks/projects Familiar with user testing methodologies like interviews, surveys, observations, diary study Troubleshoot various technical data

Easy Apply

Full-time

Depends on Experience

Global Clinical Order Manager

South San Francisco, California

•

3d ago

PTDS Global Clinical Supply Chain Management department packages and distributes Investigational Medicinal Products (IMPs) required for s clinical trials. The Global Clinical Order Management (GCOM) team prepares all packaging orders produced at our clinical packaging facilities in Kaiseraugst and South San Francisco. The GCOM Tasks & Responsibilities include: Manage in-house packaging orders and drive the on-time in-full delivery of IMPs. Be accountable for setting up Standard Packaging Design

Easy Apply

Third Party, Contract

$45 - $66

Clinical Contracts Associate

Remote

•

Today

(USA), Plano, TX, Maplegrove, MN Role Summary Working under the direction of a manager or senior contracts associate, the Clinical Contracts Associate provides technical assistance in developing, negotiating, reviewing, and processing clinical study and research contracts and budgets. This role solves problems in straightforward situations using technical experience, judgment, and precedent, and is capable of routine negotiations with limited supervision. Key Responsibilities Develops and

Full-time, Third Party

Depends on Experience

Administrative/Project Assistant II

Mountain View, California

•

Today

Job Code: Administrative/Project Assistant II Job Title: Administrative/Project Assistant II Duties: TITLE: Project Coordinator Role Purpose: As a Project Coordinator, your main responsibility will be to support clinical studies by maintaining the efficiency and organization of laboratory operations. You will maintain the laboratory inventory, prepare devices, and handle office administrative tasks for the Clinical Verification and Validation Team. This role will require you to keep

Easy Apply

Contract, Third Party

$23 - $23

Clinical Psychologist - Fresno CA

Fresno, California

•

Today

Clinical Psychologist - Veteran Disability Assessments We are seeking a dedicated Clinical Psychologist to join our team in performing medical assessments for U.S. Veterans as part of the VA\'s disability benefits process. In performing Disability Assessments, you will review behavioral health records electronically through a secure Web Portal and perform a comprehensive assessment in-person on each Veteran. Key Responsibilities: Conduct in-person disability assessments for U.S. Veterans. Revie

Full-time

USD 53.00 - 60.00 per hour

Clinical Trials jobs in California, USA