Clinical Research Coordinator II
$48kMassBiologics
Clinical Research Coordinator II Job Number: 2025-48848 Category: Research Location: Worcester, MA Shift: Day Exempt/Non-Exempt: Exempt Business Unit: UMass Chan Medical School Department: School - Populat & Quantitive Hlth Sci - W455000 Job Type: Full-Time Union Code: Non Union Position -W60- Non Unit Professional Num. Openings: 1 Post Date: Nov. 5, 2025 Work Location: Hybrid Salary Minimum: USD $48,000.00/Yr. Salary Maximum: USD $56,000.00/Yr. Position Summary Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator II is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for complex research protocols related to treatment, ancillary services, and prevention practices. Essential Functions Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAA Identify, schedule and/or conduct participant study visits, tests and/or interviews/telephone follow up calls Ensure accuracy and completion of all regulatory documentation, including local or central IRB and study data Conduct preliminary quality assurance reviews of study data Assist with financial /operational aspects of grant and contracts. May be responsible for clinical research billing review within the required timeframe Present study status reports related to assigned research projects Contribute to data presentations and Institutional Review Board (IRB) processes Track and maintain study related information in the data management system within the required timeframe Provide detailed written summaries from literature searches and related sources to serve as a resource for the study team and clinicians/PIs Contribute to the design, development, and documentation of study related data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists) Responsible for monitoring the inventory of research related supplies Document and collect data/ samples for research related procedures performed during participant study visits. Ensure clinicians and/or PI accurately document their study activities according to protocol. Monitor strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines. Identify and resolve issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance Comply with all safety and infection control standards appropriate to this position Adhere to Good Clinical Practice (GCP) guidelines and all human subject protection practices Perform other duties as required. Required Qualifications Bachelors degree in a scientific or health related field, or equivalent experience 1-3 years of related experience Ability to travel off site locations Posting Disclaimer This job posting outlines the primary responsibilities and qualifications for the role but is not intended to be an exhaustive list. Duties and expectations may evolve in response to the needs of the department and the broader institution. In alignment with our commitment to pay transparency, the base salary range for this position is listed above (exclusive of benefits and retirement). At UMass Chan Medical School, final base salary offers are determined based on a combination of factors, including your skills, education, and relevant experience. We also consider internal equity to ensure fair and consistent compensation across our teams. Please note that the range provided reflects the full base salary range for this position. Offers are typically made within the midrange to allow for future growth and development within the role. In addition to base pay, UMass Chan offers a comprehensive Total Rewards package, which includes paid time off, medical, dental, and vision coverage, and participation in a 401(a)-retirement plan, with the option to contribute to a voluntary 403(b) plan. UMass Chan welcomes all qualified applicants and complies with all state and federal anti-discrimination laws. #J-18808-Ljbffr
- ...Overview POSITION SUMMARY: Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator II is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination...SuggestedLocal area
- ...Position Summary Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator II is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory...SuggestedLocal area
- 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...Suggested
- 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...Suggested
- ...world. Together, we lead in education, research, health care delivery, and public... ...Principal Investigator (PI) or designee, the Clinical Research Coordinator is responsible for independently... ...as required. Clinical Research Coord II Conduct preliminary quality assurance...SuggestedLocal area
$48k
...the direction of the Principal Investigator or designee, the Research Coordinator II is responsible for independently carrying out multiple... ...Major Responsibilities: Administratively responsible for the clinical aspects of patient study subjects and testing. Participate...Work at office- 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...
- Responsibilities Obtain consent of research participants in accordance with the IRB-approved protocols and all applicable regulations,... ...operational aspects of grant and contracts, and may be responsible for clinical research billing review within the required timeframe. Track...Local area
- ...The University of Massachusetts Medical School is looking for a Research Coordinator. In this entry-level role, you will assist with obtaining consent from participants, maintain regulatory documentation, and support study investigators. Qualified candidates should have...
- ...UMass Chan Medical School is seeking a Clinical Research Coordinator for a dynamic role in managing research protocols. Responsibilities include coordinating regulatory activities and collecting data within a collaborative environment. Candidates will gain exposure across...
- 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...
- The University of Massachusetts Medical School is seeking a candidate for a research role that involves obtaining consent from study participants and ensuring compliance with regulatory protocols. The role demands a Bachelor's degree in a scientific or health-related field...
- The University of Massachusetts Medical School is seeking a Clinical Research Coordinator I. This role involves coordinating tasks related to human subject research, ensuring compliance with regulations, and managing data collection. The ideal candidate will have a Bachelor...
- The University of Massachusetts Medical School is seeking a Clinical Research Coordinator I to manage tasks related to human subject research. You will be responsible for coordinating regulatory activities and managing data for research protocols, ensuring compliance with...
- 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...
- A leading research institution in Massachusetts is seeking a Research Coordinator II to manage multiple complex research initiatives. This role involves providing project support, overseeing data collection and analysis, and ensuring compliance with regulatory requirements...
- ...supporting children, youth, and families, and have strong skills in care coordination and collaboration, we invite you to join our Intensive Care Coordination (ICC)/CSA team as a Care Coordinator II. In this role, you'll facilitate the Wraparound process for youth ages 0...
- ...Job Description Job Description Summary The Conventions Specialist II position is responsible to coordinate the creation of an event and each step throughout the complete process. This includes the shipment and return of each event, follow up for unreturned items...Remote workWork from home
$28.2 - $48.06 per hour
...Union: SHARE (State Healthcare and Research Employees) This position may have a signing... ...area. Refers to Medical Technologist II's or supervisory or lead staff members for... ...program. Interprets and correlates clinical test results with patient history, diagnosis...Immediate startRelocation packageMonday to FridayShift workDay shift- ...Hybrid Details On-site 3 days/week in Worcester, MA Duration 12 months to start Job Description Job Summary The Clinical Value Analysis Coordinator is responsible for leading and owning the end-to-end value analysis process across the provider organization. This role partners...Contract work3 days per week
- ...form to find jobs that suit your specificcareer interests. Clinical Coordinator Job Number : 2025-48588 Category: Administrative Professional... ...Agencies regarding the issues of various MassHealth populations. Research MassHealth regulations and interpret these regulations for...Full timeWork experience placementWork at officeShift work
- ...Position Summary: Under the supervision of the Director of Psychiatric Services, the Psychiatric Clinical Coordinator (Medical Assistant) coordinates psychiatric clinical services for specialty care patients, oversees management of psychiatric provider panels...Monday to Friday
- ...of Massachusetts Medical School is seeking an Administrative Assistant II to perform complex administrative duties supporting research projects and grants. The role involves independent coordination of tasks, communication with departments, maintaining records, and assisting...Work at office
- ...compassion - must guide what we do, as individuals and professionals, every day. Works Under The Supervision Of The Nurse Manager/Clinical Coordinator. The Registered Nurse (Rn) Assesses, Plans, Implements, Evaluates And Supervises Individual Patient Care On A Nursing Unit/...Temporary workFlexible hours
- ...role requires at least 3 years of emergency department experience and a Bachelor's degree in Nursing. This position will involve coordinating care for acutely ill patients, prioritizing real-time care needs, and engaging in hospital communications. A signing bonus may...Remote jobRelocation packageNight shift
- ...Now Hiring - Clinical Records Coordinator The Clinical Records Coordinator will be responsible: Initiates the Clinical record at time of admission including initial preparation, interim maintenance, periodic tracking, closure and filing Ensures that: Chart is prepared...Interim roleWork at officeImmediate startDay shift
- A leading medical institution in Shrewsbury is seeking a Clinical Coordinator responsible for overseeing care coordination for MassHealth members. The ideal candidate has extensive experience in clinical management, a BS in a related field or RN license, and strong leadership...Full time
- ...the direction of the Principal Investigator or designee, the Research Coordinator I is responsible for carrying out multiple complex research... ...Pathways for Perinatal Mental Health Equity (Pathways), is a clinical trial that is being conducted at Lifeline for Families. The...Contract workLocal area
$30 - $33 per hour
...) regulations. Read study protocols and extract pertinent information with guidance. Maintain proficient knowledge of hematology, clinical chemistry, coagulation, urinalysis, and fecal analysis. Operate, maintain, and troubleshoot clinical pathology analyzers with guidance...Local area- ...Overview The Clinical Pathology Laboratory is responsible for providing accurate, timely diagnostic test results for patients of... ...Cummings School of Veterinary Medicine, as well as test results for research animals. Laboratory testing includes hematology, clinical...InternshipWeekend work
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