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Overview Orthopaedics-Trauma Clinical Research Coordinator II performs a full range of clinical research duties at a skilled level and has a working knowledge of the clinical research process and the regulations that govern it. The expectation is to perform progressively more complex and comprehensive clinical research duties with an increasing level of independence, working closely with the Principal Investigator (PI). The Clinical Research Coordinator II works under the supervision of and at the direction of the PI or their designee. They cannot perform any tasks that state or local law require a license to perform. This position involves supporting clinical orthopaedic trauma studies and requires strong flexibility, exceptional time management skills, and the ability to thrive in fast-paced environments. The ideal candidate will be comfortable working in the emergency department and collaborating effectively with multidisciplinary teams in the operating room. Responsibilities Resear

Starting with 4 weeks of paid time off (pro-rated) plus 12 sick days and 9 holidays per year! Join one of Vermont's Best Places to Work for Five Years in a row! Position Purpose: The Police Liaison works embedded in area municipal police departments responding to mental health, substance abuse, domestic violence or other social service related calls with law enforcement, to provide immediate support and resource connection. The Police Liaison adheres to HCRS policy and complies with federal, state, and local regulations and supports program philosophy. Principal Responsibilities and Duties: Police Liaisons provide an array of supports to individuals including, but not limited to, assisting individuals with various challenges (financial, medical, legal, transportation, food, employment, etc.) and helping them to connect with community agencies and care providers. Police Liaisons work embedded in local police departments responding to emergency and non-emergency calls. They provide assis

Overview Clinical Research Coordinator II performs a full range of clinical research duties at a skilled level and has a working knowledge of the clinical research process and the regulations that govern it. The expectation is to perform progressively more complex and comprehensive clinical research duties with an increasing level of independence, working closely with the Principal Investigator (PI). The Clinical Research Coordinator II works under the supervision of and at the direction of the PI or their designee. They cannot perform any tasks that state or local law require a license to perform. This Clinical Research Coordiantor II will work specifically on a large, multi-center randomized trial that will compare the effectiveness of annual non-invasive stool testing verus colonoscopy for surveillance in older adults with a history of colon polyps. This is a long-term project that had an initial feasibility phase of 18 month and now is in the full trial phase of 5 years and is fund

MILL RIVER UNIFIED UNION SCHOOL DISTRICT JOB DESCRIPTION & POSTING POSITION: SPEECH-LANGUAGE PATHOLOGIST-CCC POSITION TITLE: Speech Language Pathologist-CCC, 1.0 FTE POSITION START DATE: On or about August, 20, 2025 POSITION LOCATION: Mill River Unified Union School District -Wallingford Elem. School, PreK-6th grade -Tinmouth Elem. School, PreK-6th grade -Shrewsbury Mountain School, PreK-6th grade SUPERVISED BY: Director & Assistant Director of Student Services, and Building Principals BASIC FUNCTION: The educational Speech-Language Pathologist will conduct high-quality special education evaluations as well as implement evidence-based speech-language therapy services to eligible students spanning multiple grade levels and categories of need. WORKS WITH: Students, Teachers, Administration, Parents QUALIFICATIONS: 1. The applicant must hold a current Vermont Educator's License as an Educational Speech-Language Pathologist, in addition to clinical licensure from the Vermont Office of Prof

Overview Full time, Cancer Center The Clinical Research Coordinator II performs a full range of clinical research duties at a skilled level and has a working knowledge of the clinical research process and the regulations that govern it. The expectation is to perform progressively more complex and comprehensive clinical research duties with an increasing level of independence, working closely with the Principal Investigator (PI). The Clinical Research Coordinator II works under the supervision of and at the direction of the PI or their designee. They cannot perform any tasks that state or local law require a license to perform. Responsibilities Research Operations Occasionally requiring tasks outside of defined operating hours * May arrange and/or schedule required tests and other appointments. * Understands and supports all of aspects of the study operations (including subject management/regulatory) with oversight from the investigator or their designee. * Primarily supports subject ma

Overview SIGN ON BONUS ELIGIBLE - Orthopaedics The Clinical Research Coordinator III performs a full range of clinical research duties at an advanced level and plans, organizes, leads, and performs comprehensive clinical trial duties for multiple or complex clinical trials, focusing on the overall productivity and success of the program. The expectation is to perform with limited supervision and actively participate in decisions regarding the clinical research process, often leading teams. The impact of decisions of the Clinical Research Coordinator III are wide in scope affecting both internal and external partners. They cannot perform any tasks that by state or local law require a license to perform. Responsibilities * * Research Operations- Occasionally requiring tasks outside of defined operating hours: * Mentors, onboards, trains and oversees new clinical research coordinator staff onGood Clinical Practice (GCP), Human Subjects Protection (HSP) practices,the ethical conduct of res

CULTIVATE A BETTER WORLD Food served fast does not have to be a typical fast-food experience. Chipotle has always done things differently, both in and out of our restaurants. We are changing the face of fast food, starting conversations, and directly supporting efforts to shift the future of farming and food. We hope you will join us as we continue to learn, evolve, and shape what comes next on our mission to make better food accessible to everyone. THE OPPORTUNITY As Kitchen Leader, you will learn how to prepare great food, grill meats, and saut vegetables. You are responsible for making sure our food is absolutely delicious. You'll order the food and train others to become future Kitchen Leaders. The Kitchen Leader helps ensure the quality and safety of Chipotle's delicious food every day. They see to it that the kitchen is clean, organized and well stocked; and that the equipment is properly maintained and in good condition. Throughout the process they are serving as a role model fo

Overview Clinical Research Coordinator I works closely with other research staff and is involved at a fundamental level to support basic administrative clinical trial tasks. The Clinical Research Coordinator I has no supervisory responsibilities and works under direct supervision of the Principal Investigator or designee. They cannot perform any tasks that by state or local law require a license to perform. Responsibilities * Research Operations * May arrange/schedule required appointments. * Learns and supports all of aspects of the study operations (subject management/regulatory) with substantial oversight from the investigator or their designee. * Primarily supports subject management, such as subject visit preparation, performs data entry in the Clinical Trial Management System (CTMS), scans informed consents into Electronic Medical Record (EMR) and supports data entry needs of the study. * Regulatory Affairs * Assists with compiling and maintaining essential records and documents