Clinical Scientist Jobs in Santa Clarita, CA

The Clinical Nurse Specialist (CNS) CVICU provides advanced clinical expertise in the Cardiovascular Intensive Care Unit (CVICU). This role involves setting high standards for nursing practice educating staff consulting on complex cases and contributing to the development of our CVIC More...

Acts as a specialized liaison to assist sites with a protocoltailored approach to increase efficiency of the patient identification and recruitment processAssists sites in developing and implementing patient enrollment techniquesCoordinates site specific patient recruitment and retent More...

Industry: HealthcareClinical Nurse Specialist CVICULocation: Santa Clara CAResponsibilities:Clinical Expertise: Provide expert consultation and guidance to nurses and other healthcare providers in the CVICU.Education & Mentorship: Develop and implement educational programs for nu More...

About This RoleAs a Senior Manager Aggregate Report Scientist you will be an integral part of the Safety Surveillance and Aggregate (SSA) Reports team. In this pivotal role you will oversee the pharmacovigilance processes for all aggregate reports including PSURs DSURs PADERs and loca More...

ABOUT USWe are a pioneering B2B data and SaaS platform that empowers professional real estate investors to generate consistent leads through Cold Calls SMS and Direct Mail without increasing expenditure. We leverage AI machine learning and advanced analytics to identify homeowners lik More...

About This RoleThis role reports into the Head of Aggregate Reports and will be part of the Safety Surveillance and Aggregate Reports (SSA) team. The Associate Director Pharmacovigilance Scientist is responsible for managing the processes for all Aggregate Reports such as PSURs DSURs More...

About This RoleThis role reports into the Head of Aggregate Reports and will be part of the Safety Surveillance and Aggregate Reports (SSA) team. The Associate Director Pharmacovigilance Scientist is responsible for managing the processes for all Aggregate Reports such as PSURs DSURs More...

Job Title: Clinical Data Associate Duration: 06 months contract with possible extension Shift Details: Day shift/ Fully Remote Pay Range: $30$37 /hr w2 Essential Duties and Responsibilities: Works collaboratively with Process Engineers and Statisticians in Global Manufact More...

As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigato More...

Description: The ideal candidate will have thorough knowledge of Clinical investigation of medical devices for human subjects Good Clinical Practice (ISO 14155) 21 CFR partand other applicable regulations. Roles & Responsibilities: Contribute to all clinical research activitie More...

Opportunity at a GlanceThe primary purpose of this role is to establish clinical relationships in markets where new campus  location are likely to open and to support new programs.ResponsibilitiesDevelop relationships with health organizations in potential and current markets.Dev More...

JOB TITLE: Vendor Qualification Associate I Onsite: Foster City Hybrid: 3 days a week minimum Description Client is looking for a Vendor Qualification Associate I who will report to the Senior Manager of Vendor Outsourcing. The candidate will be responsible for ensuring high quality More...

As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigato More...

Coordinates investigator/ site feasibility and identification process as well as study startup.Monitors project timelines and patient enrollment implements respective corrective and preventive measures.Reviews monitoring visit reports for all visit types and ensures reporting complian More...

We are seeking a selfmotivated and independent Data Scientist to solve complex problems and influence user experience strategies and product decisions through datadriven insights. You will join a newly established hybrid UX Research team comprising Data Scientists Quantitative Researc More...

As a Clinical Research Associate you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical site More...

Description: Works collaboratively with Process Engineers and Statisticians in Global Manufacturing Sciences and Technology (GMSAT) Statistical Sciences & Analytics (SS&A) team to meet project deliverables and timelines to author and approve Continued Process Verification (CPV) relat More...

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.You will:Act as the main line of communication between the project team spon More...

Coordinates investigator/ site feasibility and identification process as well as study startup.Monitors project timelines and patient enrollment implements respective corrective and preventive measures.Reviews monitoring visit reports for all visit types and ensures reporting complian More...

We are seeking a selfmotivated and independent Data Scientist to solve complex problems and influence user experience strategies and product decisions through datadriven insights. You will join a newly established hybrid UX Research team comprising Data Scientists Quantitative Researc More...