Clinical Research Jobs in Saint Paul, MN
Clinical Research Jobs in Saint Paul, MN

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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...
About This Role Leading and taking full accountability in the successful creation ownership and execution of US Medical Affairs (USMA) operational processes and activities the Sr Manager Medical Affairs Operations Lead (specialty Care) is a critical member of the US Medical Affairs te More...
The Manager Regulatory Affairs US Advertising & Promotion combines knowledge of scientific regulatory and business issues to enable products that are developed manufactured or distributed to meet required legislation. Has responsibility for 12 of the following: therapeutic area pr 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...
General SummaryUnder limited supervision is responsible for the collection of the account balances from all third party payors and patients for services rendered at UMMC Kernan and Specialty Hospital. Manages the Cash Posting area and Followup. Develops and maintains the policies and More...
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...
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...
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