Clinical Research Coordinator I: IRB & Study Operations
University of Massachusetts Medical School
The University of Massachusetts Medical School is seeking a Clinical Research Coordinator I to manage research protocols related to human subjects. Responsibilities include securing participant consent, coordinating study visits, and ensuring compliance with regulatory standards. This position requires a Bachelor's degree in a scientific or health-related field and offers a salary complemented by comprehensive benefits including health coverage and retirement plans. Ideal candidates should have 0-1 year of related experience and be willing to travel off-site as necessary. #J-18808-Ljbffr University of Massachusetts Medical School
- ...UMass Chan Medical School is seeking a Clinical Research Coordinator for a dynamic role in managing research protocols. Responsibilities include... ...environment. Candidates will gain exposure across various studies, allowing them to develop expertise in clinical trial management...Operations
- ...Massachusetts Medical School is seeking a candidate for a research role that involves obtaining consent from study participants and ensuring compliance with... ...regulatory documentation, and assisting with various operational aspects of research. A comprehensive benefits...Operations
- ...Investigator (PI) or designee, the Clinical Research Coordinator is responsible for... ...to a wide range of clinical studies and investigators across UMass... ...-facing research, study operations, regulatory compliance, and... ...participants in accordance with the IRB approved protocols and all...OperationsLocal area
- ...Investigator (PI) or designee, the Clinical Research Coordinator III is responsible for... ...in accordance with the IRB approved protocols and all... ...maintaining and terminating study subjects for multiple protocols... ...Assist with financial /operational aspects of grant and contracts...SuggestedLocal area
- ...Investigator (PI) or designee, the Clinical Research Coordinator II is responsible for... ...team conducts an array of studies related to addressing... ...participants in accordance with the IRB approved protocols and all... ...Assist with financial /operational aspects of grant and contracts...SuggestedLocal area
- A reputable medical school in Worcester, Massachusetts, is looking for a Clinical Research Coordinator II to join their dedicated research team. The successful candidate will coordinate human subject research involving registration and management of data. This role requires...
- The University of Massachusetts Medical School is seeking a Clinical Research Coordinator II for human subject research. Responsibilities include obtaining consent, managing data, and ensuring regulatory compliance. This role supports groundbreaking research on the gut...
- Responsibilities Obtain consent of research participants in accordance with the IRB-approved protocols and... .../or conduct participant study visits, interviews, and... ...Assist with financial/operational aspects of grant and... ...may be responsible for clinical research billing review...Local area
- ...University of Massachusetts Medical School is looking for a Research Coordinator. In this entry-level role, you will assist with obtaining consent... ..., maintain regulatory documentation, and support study investigators. Qualified candidates should have a Bachelor's...
- A prominent educational institution in Massachusetts is seeking a Clinical Research Coordinator. The role involves obtaining participant consent, coordinating studies, and maintaining regulatory compliance. Applicants should have a Bachelor’s degree in a scientific field...
- The University of Massachusetts Medical School is seeking a Clinical Research Coordinator I. This role involves coordinating tasks related to human... ...will obtain consent from research participants, schedule study visits, and document regulatory processes. This position offers...
- The University of Massachusetts Medical School is seeking a Clinical Research Coordinator I to manage tasks related to human subject research. You... ...the ability to travel to off-site locations for participant studies. #J-18808-Ljbffr University of Massachusetts Medical...
- The University of Massachusetts Medical School is seeking a Clinical Research Coordinator III, responsible for coordinating human subject research projects and ensuring regulatory compliance. The role involves obtaining consent, managing data collection, and training research...
- The University of Massachusetts Medical School seeks a Clinical Research Coordinator to oversee human subject research activities, ensuring regulatory compliance and accurate data management. This open-rank posting accommodates varied experience levels, with duties including...
- ...Overview The Clinical Pathology Laboratory is responsible for providing accurate, timely... ...Medicine, as well as test results for research animals. Laboratory testing includes... ...serology and parisitology along with the operation of automated laboratory instrumentation...OperationsInternshipWeekend work
$30 - $33 per hour
...procedures according to protocol, SOP and GLP. Operate, maintain, and perform basic... ...Biological sample processing. Perform and review study ordered parameters and computer input of... ...Maintain proficient knowledge of hematology, clinical chemistry, coagulation, urinalysis, and...Local area$30 - $33 per hour
...protocol, SOP and GLP. Operate, maintain, and perform... .... Perform and review study ordered parameters and... ...knowledge of hematology, clinical chemistry, coagulation... ...early-stage contract research organization (CRO). We... ...positioned to coordinate worldwide resources and...Contract workLocal areaWorldwideFlexible hours- ...build or grow their private practice. Headway provides the tools, resources, and support to help you navigate insurance, streamline operations, and focus on delivering quality care - on your own terms. About you You’re a fully licensed psychiatrist with your DEA...OperationsBi-weekly payFor contractorsPrivate practice
- ...every day. Works Under The Supervision Of The Nurse Manager/Clinical Coordinator. The Registered Nurse (Rn) Assesses, Plans, Implements,... ...Performs Other Duties As Assigned Or Directed To Ensure Smooth Operation Of The Department/Unit. # Demonstrates Competency In The...Operations
- ...every day. Works Under The Supervision Of The Nurse Manager/Clinical Coordinator. The Registered Nurse (Rn) Assesses, Plans, Implements,... ...Performs Other Duties As Assigned Or Directed To Ensure Smooth Operation Of The Department/Unit. # Demonstrates Competency In The...Operations
- ...every day. Works Under The Supervision Of The Nurse Manager/Clinical Coordinator. The Registered Nurse (Rn) Assesses, Plans, Implements,... ...Performs Other Duties As Assigned Or Directed To Ensure Smooth Operation Of The Department/Unit. # Demonstrates Competency In The...Operations
- ...start or grow their private practice. Headway provides the tools, resources, and support to help you navigate insurance, streamline operations, and let you focus on what matters most - your patients. About you You’re a fully licensed psychiatric nurse practitioner...OperationsBi-weekly payFull timeFor contractorsPrivate practiceFlexible hours
- ...day. Works under the supervision of the nurse manager/clinical coordinator. The registered nurse (RN) assesses, plans, implements, evaluates... ...other duties as assigned or directed to ensure smooth operation of the department/unit. # Demonstrates competency in the...Operations
- ...reference services, assist patrons with research, guide them through online resources, troubleshoot... ...technology, and support library operations from opening to closing. This part‑time,... ...e‑readers and devices, managing group study room bookings, and #J-18808-Ljbffr Shrewsbury...OperationsPart timeSeasonal work
- The University of Massachusetts Medical School is looking for a Clinical Research Assistant. In this role, you will assist in clinical operations such as developing tools for studies, collecting and storing data, and scheduling patient interactions. Ideal candidates demonstrate...Operations
- ...Negotiable Job Duration: Locums About the Facility The facility operates as an inpatient and outpatient center in Massachusetts... ...radiologist will interpret musculoskeletal and neurological imaging studies in a hybrid facility environment serving inpatient, outpatient,...OperationsLocumShift workDay shift
- ...Together, we lead in education, research, health care delivery, and... ...of people around the globe. Clinical Research Assistant Job Number... ...Major Responsibilities Clinical Operations Assist PI in development of... ...protocol-specific tools to aid in study documentation Collect record,...OperationsShift work
- ...manufacturing engineering activities in support of manufacturing operations within established quality systems, FDA regulations, and ISO... ...protocols and reports. Participate in PFMEA activities, time studies, and value stream mapping exercises. Assist in evaluating product...OperationsHourly pay
- ...Clinical Data Management Leader Provide leadership, strategic planning, direction and... ...planning, vendor oversight, EDC build and study timelines, etc. Perform or provide... ...activities Develop and manage standard operation procedures (SOP and CLPs) for clinical investigation...Operations
- ...therapy providers, Reliant offers unmatched clinical support, professional development, and... ...to support our partners. With operations in 44 states and more than 900 communities... ...leadership skills through collaboration, self-study, and continuing education • Maintain a...OperationsFull timeContract workReliefFlexible hours
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