Clinical Research Jobs in London, KY

At Adtalem Global Education we are committed to empowering students and transforming lives through education. As a Senior Regulatory Affairs Analyst you will play a critical role in ensuring compliance with federal state and accreditor regulations helping to shape policies and process More...

About this roleThe Field Director Medical Science Liaisons Immunology role is a part of US Medical Affairs a strategic partner within Biogen that helps inform medical practice across our therapeutic areas and pipeline to improve meaningful patient outcomes. The Field Director will be More...

Vice President Regulatory AffairsHybrid/Remote Options AvailableAre you a strategic leader with a passion for regulatory compliance and higher education Join our team as Vice President of Regulatory Affairs where you will shape compliance strategies build key regulatory relationships More...

About This Role The Senior Manager GCP Quality Assurance & Governance in R&D Quality and Compliance provides global strategic leadership for quality and oversight of quality activities in Biogen R&Ds ongoing clinical research and development processes and programs partneri 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 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...

At Adtalem Global Education we are committed to empowering students and transforming lives through education. As a Senior Regulatory Affairs Analyst you will play a critical role in ensuring compliance with federal state and accreditor regulations helping to shape policies and process 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...

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...

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...

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...

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...

About the Role:We are seeking a highly experienced and visionary Senior Manager for our AI Foundation team. This role is pivotal in driving the strategy development and implementation of AI capabilities services and solutions to assist our organizations AI initiatives that is a mix of 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...

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...

*Can be remote in the US or EUProvides specialist medical and scientific strategic and operational input into core medical affairs activities such as: healthcare professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value More...

insightsoftware is hiring an experienced Regulatory & Export Compliance Manager to support the business develop continuously enhance scale and manage insightsoftwares regulatory and export compliance including matters pertaining to antibribery/anticorruption and ethics. A successf More...

Job Title: Field Medical Director (Remote Southeast Region) Job Location: Home Creek VA 24614 USA Job Location Type: Remote Job Contract Type: Fulltime Job Seniority Level: MidSenior level Company OverviewImmunityBio Inc. (NASDAQ: IBRX) is a commercialstage biotechnology company dev 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...