Clinical Research Coordinator I (Hybrid) - Radiology Washington University in St LouisClinical Research Coordinator I (Hybrid) - RadiologySt. Louis, MO$49,200–$73,800 / yearPrimary Duties & Responsibilities: Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants' progress in the study; analyzes, investigates and reports adverse events; makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency. Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.
Clinical Research Coordinator I - Hematology Washington University in St LouisClinical Research Coordinator I - HematologySt. Louis, MO$49,200–$73,800 / yearPrimary Duties & Responsibilities: Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants' progress in the study; analyzes, investigates and reports adverse events; makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency. Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.
Clinical Research Coordinator I - Obstetrics and Gynecology Washington University in St LouisClinical Research Coordinator I - Obstetrics and GynecologySt. Louis, MO$49,200–$73,800 / yearPrimary Duties & Responsibilities: Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants' progress in the study; analyzes, investigates and reports adverse events; makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency. Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.
Senior Contract Specialist (Remote) - Office of the Vice Chancellor for Research Washington University in St LouisSenior Contract Specialist (Remote) - Office of the Vice Chancellor for ResearchSt. Louis, MORemoteSkills: Agency Law, Communication, Contract Agreements, Contract Law, Contract Modifications, Contract Negotiations, FDA Compliance, Insurance, Licensing Agreements, Paralegal Education, Patent Licensing, Prioritization, Research Compliance, Self-Organization (Business), Sound Judgment, Working Independently, Writing. Additional responsibilities include: Maintain electronic records that are consistent and current; this includes review of documents to ensure appropriateness and completeness; ensures integrity of data captured in contract tracking system; provide strategic data to senior administration through reports as requested.
Clinical Research Coordinator I - Surgery Oncology Washington University in St LouisClinical Research Coordinator I - Surgery OncologySt. Louis, MO$49,200–$73,800 / yearPrimary Duties & Responsibilities: Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants' progress in the study; analyzes, investigates and reports adverse events; makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency. Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.
Research Assistant - Neurosurgery Washington University in St LouisResearch Assistant - NeurosurgerySt. Louis, MO$17.10–$29.09 / hourOur work primarily uses advanced magnetic resonance imaging (MRI) data, such as functional MRI (fMRI) for studying the brain through functional connectivity and other metrics of normal and abnormal function. We work with a range of pediatric patients who have medical conditions such as Chiari Malformaiton Type 1 (CM1), medically refractory epilepsy, and cerebral palsy (CP) that volunteer for research participation before or after surgical intervention as well as alongside routine clinical monitoring care.
Clinical Research Coordinator II - Pulmonary & Critical Care Medicine Washington University in St LouisClinical Research Coordinator II - Pulmonary & Critical Care MedicineSt. Louis, MO$54,600–$81,900 / yearImplements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants' progress in the study; analyzes, investigates and reports adverse events; makes decisions as when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency. Assists investigators as coordinator of clinical research studies which range from moderate to significant complexity; may be responsible for multiple research studies simultaneously; acting as a liaison with the school, sponsoring agency, study participants, and sub-investigators from other divisions; responsible for managing and recording all phases of study protocol as required by sponsoring agency to ensure compliance.
Clinical Research Coordinator I - Cardiology Washington University in St LouisClinical Research Coordinator I - CardiologySt. Louis, MO$49,200–$73,800 / yearPrimary Duties & Responsibilities: Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants' progress in the study; analyzes, investigates and reports adverse events; makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency. Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.
NewResearch Lab Manager - Pulmonary & Critical Care Medicine Washington University in St LouisResearch Lab Manager - Pulmonary & Critical Care MedicineSt. Louis, MO$63,400–$115,000 / yearThe screenings will include criminal background check and, as applicable for the position, other background checks, drug screen, an employment and education or licensure/certification verification, physical examination, certain vaccinations and/or governmental registry checks. If you are unable to use our online application system and would like an accommodation, please email CandidateQuestions@wustl.edu or call the dedicated accommodation inquiry number at 314-935-1149 and leave a voicemail with the nature of your request.
Research Technician I - Pediatrics Gastroenterology Washington University in St LouisResearch Technician I - Pediatrics GastroenterologySt. Louis, MO$16.54–$22.35 / hourThe screenings will include criminal background check and, as applicable for the position, other background checks, drug screen, an employment and education or licensure/certification verification, physical examination, certain vaccinations and/or governmental registry checks. If you are unable to use our online application system and would like an accommodation, please email CandidateQuestions@wustl.edu or call the dedicated accommodation inquiry number at 314-935-1149 and leave a voicemail with the nature of your request.
Senior Project Manager (St. Louis-Based; No Travel Required) Alberici CorpSenior Project Manager (St. Louis-Based; No Travel Required)Saint Louis, MOLouis, Missouri with more than 1,200 employees and nearing $2B in revenue, Alberici is a diversified construction company that partners with leading organizations throughout North America to build their most challenging and important projects. This individual will also be responsible for supervising subcontractor performance, ensuring the project meets quality and performance specifications and regulatory requirements, managing the start-up of the project, reviewing costs against estimates for each total project, and updating labor productivity reports.
Sr. Nutritionist, Applied Nutrition Research Nestle SASr. Nutritionist, Applied Nutrition ResearchSt. Louis, MO$82,000–$116,000 / yearInitiate and lead research projects aligned to Nestlé Purina's strategic areas related to pet health through nutrition Translate research findings into product claims, technical communications, and commercialization opportunities Function as a project team leader including providing project leadership and completing required documentation in a timely manner Formulate research hypotheses, design experimental plans, and execute scientific studies Conduct all activities in compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and all required Company Policies & Procedures Leverage veterinary and consumer insights to drive innovation that promotes health and wellness of dogs and cats Stay current in nutrition literature and intellectual property and propose new research approaches, methodologies, and technologies Publish research in peer-reviewed journals, present at key industry conferences, and participate in Nestlé Purina-sponsored symposia to introduce innovations Maintain collaborations with academic institutions, veterinary specialists, and external scientific experts Requirements PhD in nutrition or related field Other Experience designing, managing, and publishing clinical research in animal nutrition is preferred Diet formulation experience is preferred Technical/functional knowledge in the area of metabolism or gastrointestinal physiology is preferred Willingness to travel up to 10% The approximate pay range for this position is $82,000 to $116,000. Come prepared to use your deep technical understanding and scientific knowledge along with strong communication and presentation skills to develop new technologies and provide expertise and insights to companion animal nutrition.
Research Nurse Coordinator l (Hybrid) - Neurology Washington University in St LouisResearch Nurse Coordinator l (Hybrid) - NeurologySt. Louis, MO$56,200–$96,100 / yearWe have an ongoing clinical study to collect matched blood and cerebrospinal fluid from patients with memory concerns in the clinic, and will be launching a new study called the Study to Understand Novel Biomarkers in Researching Dementia (SUNBIRD) to validate blood biomarkers for Alzheimer's disease in a large clinic-based cohort. Basic Life Support - American Heart Association, Basic Life Support - American Red Cross, Registered Nurse - Illinois Department of Financial and Professional Regulation, Registered Nurse - Missouri Division of Professional Registration.
Clinical Research Coordinator III - Pediatrics Gastroenterology Washington University in St LouisClinical Research Coordinator III - Pediatrics GastroenterologySt. Louis, MO$58,300–$90,400 / yearYou will work closely with other team members and healthcare professionals to recruit and enroll study participants, explain the purpose of study and obtain informed consent from participants, conduct study visits in the hospital and the participant's home, ensure compliance with protocol guidelines and requirements of the IRB and IACUC, enter data, assist with lab procedures, and perform data analyses. Serves as responsible for the development of forms, questionnaires and the application of research techniques; assists in writing instructional procedure manuals for study progress, data collection and coding; reviews journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in the planning of new studies.
Research Lab Manager - Neurology Washington University in St LouisResearch Lab Manager - NeurologySt. Louis, MO$63,400–$115,000 / yearThe position is responsible for enabling the lab to generate state-of-the-art multi-omic libraries (single-cell RNA-seq, ATAC-seq, spatial transcriptomics, etc.) from precious human and mouse brain tissue samples to understand the biology of human aging, with a focus on neurodegenerative diseases and personalized medicine. Oversees and directs all support activities of the lab including human resources, budgets, facility maintenance, purchasing, supplies, materials, equipment, project timelines, milestones, and deliverables for NIH-funded and other externally sponsored research projects.
Clinical Research Coordinator II (West County) - Allergy & Immunology Washington University in St LouisClinical Research Coordinator II (West County) - Allergy & ImmunologySt. Louis, MO$54,600–$81,900 / yearImplements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants' progress in the study; analyzes, investigates and reports adverse events; makes decisions as when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency. Coordinates the development of forms, questionnaires and the application of research techniques; assists in writing instructional procedure manuals for study progress, data collection and coding; reviews journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in the planning of new studies.
Project Manager Research (Hybrid) - Neurology Washington University in St LouisProject Manager Research (Hybrid) - NeurologySt. Louis, MO$58,400–$99,700 / yearSkills: Analytical Thinking, Communication, Confidentiality, Detail-Oriented, Group Problem Solving, Interpersonal Communication, Microsoft Office, Multitasking, Organizational Planning, Project Administration, Timeline Management, Working Independently. The screenings will include criminal background check and, as applicable for the position, other background checks, drug screen, an employment and education or licensure/certification verification, physical examination, certain vaccinations and/or governmental registry checks.
Manager Division Clinical Research - Medical Oncology Washington University in St LouisManager Division Clinical Research - Medical OncologySt. Louis, MO$75,200–$128,800 / yearSkills: Academic Programs, Accounting, Business Administration, Clinical Research Coordination, Clinical Research Methods, Compliance Requirements, Employee Management, FDA Compliance, FDA Regulations, Financial Resources Management, Grant Funding, Health Care, Institutional Review Board (IRB), Leadership, Oral Communications, Problem Solving, Project Planning, Regulatory Compliance, State Regulations, Written Communication. Responsible for overall clinical research study planning, coordinating, and execution of all study-related activities, including extensive interaction wth the Internal Review Board (IRB), study sponsors, and investigators.
Public Health Research Coordinator I (Hybrid) - Siteman Cancer Center Washington University in St LouisPublic Health Research Coordinator I (Hybrid) - Siteman Cancer CenterSt. Louis, MO$23.63–$35.49 / hourPrimary Duties & Responsibilities: Routinely implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; may establish record-keeping systems; makes assessments and determinations of participants' progress in the study and records progress into database; may analyze, investigate, and report adverse events; may make decisions as when to notify investigator of emergent issues, when to recommend stopping participant inclusion, and/or to make and/or recommend adjustment of the protocol of particular participants; works with investigator and HRPO to resolve IRB/protocol management issues and recommends corrective action as appropriate; may serve as liaison with funding or sponsoring agency. Routinely recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria, medical record review, and/or observations/analysis in participant interviews; develops and prepares informed consent packets for study participants; and confers with participants to explain purpose of study and obtain completed informed consent packets; explains study processes and procedures to address participant/family concerns; administers/scores tests and/or evaluates all assessments to ensure they are completed in a timely manner.
Public Health Research Coordinator II (Hybrid) - Siteman Cancer Center Washington University in St LouisPublic Health Research Coordinator II (Hybrid) - Siteman Cancer CenterSt. Louis, MO$54,600–$81,900 / yearRoutinely and with increasing independence implements manages, and ensures timely completion of all phases of study/protocol; assists investigator with development of participant recruitment plan; has increasing responsibility for: ensuring compliance with protocol guidelines and requirements of regulatory agencies; establishing record-keeping systems; making assessments and determinations of participants' progress in the study and recording results into study database; analyzing, investigating, and reporting adverse events; making decisions as when to notify investigator of emergent issues, when to recommend stopping participant inclusion, and/or to make and/or recommend adjustment of the protocol of particular participants; resolving IRB/protocol management issues and recommends corrective action as appropriate; and serving as liaison with funding or sponsoring agency. Assists investigators as coordinator of a complex clinical research study; may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community, and study participants; has increasing responsibility for managing and recording all phases of study protocol as required by sponsoring agency to ensure compliance.