Clinical Study Administrator Jobs in Santa Clarita, CA

Take your career to the next level and be involved in study startup processes in the US. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. HomebasedYou will:Supports all processes critical for site activ More...

Your role in the global Study Startup team will cover three main areas; Departmental support Quality Control and Assurance and Training.Departmental Responsibilities: Develop tracking tools for the Study Startup departmentPrepare departmental reportsPlan organise and fo More...

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...

Job Title: Healthcare Administrator Location: Remote We are currently seeking candidates who meet the following qualifications: Responsibilities: Manage the daytoday operations of the healthcare facility including staffing budgeting and scheduling. Ensure compliance with all healthca More...

Job Title: PeopleSoft Administrator Location: Remote We are currently seeking candidates who meet the following qualifications: Key Responsibilities: Install configure and maintain PeopleSoft environments (e.g. PeopleSoft HCM PeopleSoft Finance). Perform regular system monitoring a 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...

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 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...

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...

Senior Database Administrator role requires 7 years of handson experience as MS SQL Administrator and 3 years of experience with Oracle and PostgreSQL to maintain reliable fault tolerant DB infrastructure for our growing customer base. Successful candidates will be responsible for man More...

Job Title: Office 365 Administrator Location: Remote We are currently seeking candidates who meet the following qualifications: Responsibilities: Administer and manage the Microsoft 365 environment including Exchange Online SharePoint Teams OneDrive and related services. Monitor syst More...