Clinical Research Jobs in Hawthorne, NV

About This RoleThe Medical Director Nephrology (Immunology) role is a part of Specialty Care North America (US) Medical Affairs a strategic partner within Biogen that helps inform medical practice across our therapeutic areas and pipeline to improve meaningful patient outcomes. As a k More...

The Associate Scientific/Scientific Director provides medical and scientific strategic and operational input into core medical affairs activities such as: health care professional and provider interactions (Payers Patients Prescribers and Providers); generation of clinical and scienti More...

About This Role We are seeking a dynamic and experienced Associate Director Field Medical Training & Excellence Global Medical Affairs to enhance the performance and capabilities of our Field Medical teams worldwide. This critical role integrates therapy area expertise Field Medi More...

The Senior Associate Counsel Clinical Trials and Research provides legal support for clinical trial and research activities across the University of Maryland Medical System (UMMS). This role involves refining processes to streamline timetoactivation for clinical trials standardizing c More...

The Senior Clinical Project Manager reports directly to the Director Clinical Affairs and plays a critical role within TMC. This individual will lead all of the Companys clinical research projects including strategy and budgetary planning and management. As the Clinical Affairs More...

The Director of Network Strategy is responsible for leading the strategic planning and optimization of Milestone Ones partnership with clinical research sites. The position requires a strong analytical mindset crossfunctional collaboration and strong leadership skills. This role will More...

The Director of Network Strategy is responsible for leading the strategic planning and optimization of Milestone Ones partnership with clinical research sites. The position requires a strong analytical mindset crossfunctional collaboration and strong leadership skills. This role will 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 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...

(The role requires weekly to cover PST time for a couple of days) The Scientific Affairs Manager (SAM) is responsible to inform engage and influence key stakeholders (KSH) at strategic pharma and biotech companies regarding scientific and clinical data supporting Guardant Health 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...

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...

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...

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...

Department /Resource Management and TrainingLine management of Site Contract Specialists in the North America and Latin AmericaOversees the workload and utilization of assigned staff in the region and allocates resourcesMonitors assigned staff performance and takes part in perfor 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 USResponsibilities:Advise clients project teams sites data safety monitoring boards regulatory agen More...

Resource Management and Training:Participation in QM resource allocationResource allocation of QA auditorsFacilitation of professional development and career advancement of Quality Management staffAdministrative supervision of Quality Management staff jointly with Senior Director Qual 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...

About the RoleThis role is a member of the Clinical Trial Accelerator Unit (CTAU) taking broad responsibility for accelerating Study Start Up activities harmonizing processes and providing startup expertise to studies and programs to which they are assigned to ensure study teams meet More...