Clinical Research Jobs in Thousand Oaks, CA

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 official title for this role will be Regional Project Lead.The Regional Project Lead manages and coordinates activities of project teams in designated countries and ensures consistency of Clinical Operations processes across regions. They ensure meeting study milestones are met by 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...

Securities Research AnalystDo you have experience in equity research and analysis or capital markets Our Securities Research Group supports the portfolio management team which manages over $250 billion in AUM and serves highnetworth private clients and some of the worlds preeminent in More...

Job Title: Medical Director Global Medical Affairs Lead Diabetes and Metabolism US Job Location: United States Job Location Type: Remote Job Contract Type: Fulltime Job Seniority Level: HOW MIGHT YOU DEFY IMAGINATIONIf you feel like you’re part of something bigger it’ More...

Description: Duration 12 months contract with extension possibility Location Foster City CA Job Description We are seeking a highly motivated and talented Research Associate III to join the flow cytometry core team within the Research department. The successful candidate wi More...

As a Lead Project Manager your role will consist of two parts: Project Management and Corporate/Departmental Assignments. Project Management responsibilities include:Management of small (<5 countries and/or limited services) and medium sized (515 countries and/or full service) More...

The Site Contract Specialist can be based anywhere in the United States. The core responsibilities of this role include:Facilitating negotiations of site agreements and budgets to ensure alignment with the site activation plan Customizing and preparing country More...

The Site Contract Specialist can be based anywhere in the United States. The core responsibilities of this role include:Facilitating negotiations of site agreements and budgets to ensure alignment with the site activation plan Customizing and preparing country 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...

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...

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...

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...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.HomeBased in the United StatesResponsibilities:Advise clients project teams sites data safety monitoring boards More...

Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients worldwide. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The com More...

Description: Job Title: Clinical Trials Management Associate II Location: Foster City CA Duration: 06 months with possible extension Shift Details: 1st shift/ Monday Friday 8am5pm/business hours Essential Duties and Responsibilities Leads or manage components of Phase I II More...

Description: Must meet all requirements for Clinical Project Assistant position and have demonstrated proficiency in all relevant areas. Provides administrative assistance in site selection study implementation and ongoing coordination of study sites either directly or via CROs. Moni More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

We are seeking a dedicated and experienced Onsite Traveling Clinical Instructor to join our team. This fulltime position involves traveling 75% of the time taking nurses to clinical sites across the country. The ideal candidate must hold an Illinois Nursing License and a Compact Nursi More...