Clinical Research Regulatory Coordinator I
$20.16 - $29.01 per hourMass General Brigham
Clinical Research Regulatory Coordinator I
Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.
The Clinical Research Regulatory Coordinator I (CRRCI) works under general supervision to ensure the regulatory requirements for clinical trials are met. This position involves working with clinical teams, Institutional Review Boards (IRB), clinical trial sponsors and federal regulatory agencies. The CRRCI will be trained on the institutional and federal regulations governing clinical research. This position does not involve patient contact.
Principal Duties and Responsibilities:
- Maintain and organize study specific regulatory binders
- Prepare and submit protocol amendments, continuing reviews, and safety reports to the IRB
- Revise informed consent documents to include new risk information and/or updated protocol requirements through the course of the study
- Manage adverse event and deviation/violation/exception documentation for all enrolled patients and report to the sponsor and IRB as required
- Submit Data and Safety Monitoring Reports
- Maintain source documentation of correspondence with the IRB, investigators, and sponsors throughout the clinical trial process
- Collect, complete, and submit essential regulatory documents to various regulatory entities
- Participate in monitoring visits and file all monitoring visit correspondence
- Ensure appropriate documentation of delegation and training for all study staff members
- Maintain screening and enrollment logs
Skills/Abilities/Competencies Required:
- Careful attention to detail
- Good organizational skills
- Ability to follow directions
- Good communication skills
- Computer literacy
- Working knowledge of clinical research protocols
Qualifications:
Education:
Bachelor's Degree Related Field of Study required
Experience:
Knowledge, Skills and Abilities:
- Careful attention to detail.
- Good organizational skills.
- Ability to follow directions.
- Computer literacy.
- Working knowledge of clinical research protocols.
Additional Job Details (if applicable):
Remote Type
Remote
Work Location
101 Merrimac Street
Scheduled Weekly Hours
40
Employee Type
Regular
Work Shift
Day (United States of America)
Pay Range
$20.16 - $29.01/Hourly
Grade
5At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package.
EEO Statement:
0100 Mass General Brigham Incorporated is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran's Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at View phone number on click.appcast.io.
Mass General Brigham Competency Framework
At Mass General Brigham, our competency framework defines what effective leadership "looks like" by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.
- ...About Company: Evolution Research Group (ERG) is dedicated to... ...delivering high-quality Phase I–IV clinical trial execution to help... ...: The Clinical Research Coordinator is responsible for the overall... ...(IRBs) and other outside regulatory organizations, as required....RegulatoryWork at office
- ...GENERAL OVERVIEW:This job plans, coordinates, and manages the activities... ...the initiation and completion of clinical trials, sponsored by internal, industry... .... Maintains compliance with all regulatory bodies associated with human subject research.ESSENTIAL RESPONSIBILITIES:...RegulatoryFull timeFor contractorsLocal area
- DescriptionJob Summary: Collects data for clinical trials research, following general directions.... ...study documentation for submission to regulatory bodies (e.g., IRB) for pre-... ...or external clinical sites, and data coordinating centers as applicable; and developing...RegulatoryFor contractorsFor subcontractorLocal area
- Nemours is seeking a Clinical Research Coordinator to join our Nemours Children's Health team in Wilmington, DE.The Clinical Research Coordinator... ...at Nemours Children's Hospital Delaware by assisting in regulatory document preparation and collection, in-servicing research...Regulatory
- DescriptionJob Summary: Collects data for clinical trials research, independently. Prepares and/or... ...of study documentation to regulatory bodies (e.g., IRB) for pre-implementation... ...or external clinical sites, and data coordinating centers as applicable; and developing...RegulatoryFor contractorsFor subcontractorLocal area
- Independently coordinates complex (i.e. interventional, therapeutic greater than minimal risk) clinical research protocols with minimal direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. Collaborates...RegulatoryInternshipFlexible hours
$31 per hour
...professionals are continuously discovering clinical innovations and enhanced access to the... ..., equipment, technologies and research protocols. We have a commitment to our... ...Short DescriptionThe Clinical Research Regulatory Coordinator ensures regulatory compliance and accurate...RegulatoryFull timePart time- ...the University of Virginia School of Medicine is seeking a Clinical Research Coordinator 1 (CRC 1), Non-Licensed to support clinical research... ...with study coordination, data collection and management, regulatory compliance, and clinical research administration.ResponsibilitiesUnder...Regulatory
- ...home to one of the leading clinical trial networks in the country... ...and the expertise of clinical research for all patients, at... ...research activities. The Research Coordinator I will assist in the management... ...research protocols and regulatory complianceMaintains a professional...RegulatoryFull timeWork at office
$50k - $52k
Clinical Research Coordinator Title: Clinical Research CoordinatorLocation: Frontage Clinical Services, Inc. in Secaucus, NJReports to: Manager... ...desirable.• Solid knowledge of Good Clinical Practices and FDA regulatory requirements. • Good communication skills with the...RegulatoryContract workTemporary workImmediate start- ...years of directly related experience. JOB DESCRIPTION:The Clinical Research Coordinator obtains human subject data for clinical research... ...to Good Clinical Practice (GCP) activities and/or other regulatory activities.Schedules, coordinates, and participates in the...RegulatoryContract workFor contractorsWork at officeLocal area
- ...world-renowned medical and research center, we strive to provide... ...with general supervision, to coordinate research projects. This position... ...ensures quality control of clinical or basic research data in... ...telehealth or in-person. Coordinate regulatory aspects of the trial...RegulatoryFull time
$17.65 - $31.05 per hour
We are seeking a Clinical Research Coordinator in the department of Urology. Researchers at Johns Hopkins University conduct clinical trials and... ...and provide administrative support for research-related regulatory issues.Specific Duties & ResponsibilitiesCoordinate all activities...RegulatoryFull timeWork experience placement- ...UniversityEmory University is a leading research university that fosters... ...; innovative therapies and clinical trials; comprehensive... ...candidates for the Clinical Research Coordinator II position. Position... ...with sponsors.Prepares regulatory submissions.With appropriate...Regulatory
- ...Qualifications: Bachelor’s degree and five years experience as clinical research coordinator or equivalent experience.Job Summary: The Senior Clinical... ...to Good Clinical Practice (GCP) activities and/or other regulatory activities. Under the direction of the PI, supervises and...RegulatoryFor contractorsLocal area
$48k - $66k
...TypePermanent Staff (SHRA)Position TitleSoc/Clin Research Assistant - AdvancedSalary Grade... .../ GN10Working TitleClinical Research Regulatory Coordinator-CEDASPosition Number20073916Vacancy... ...We promote health and provide superb clinical care while maintaining our strong tradition...RegulatoryPermanent employmentFull timePart timeH1bLive inWork at officeLocal areaAfternoon shift$30 per hour
Job TitleClinical Research CoordinatorJob DescriptionConcentric Methods is seeking an experienced Clinical Research Coordinator to independently provide support services to the NIH.The... ...workshops, including the course Ethical and Regulatory Aspects of Clinical Research, and the...RegulatoryHourly pay- ...world-renowned medical and research center, we strive to provide... ...with limited supervision, to coordinate research projects. This position... ...ensures quality control of clinical or basic research data in... ...processing site. Experience in regulatory submissions, IRB protocols,...RegulatoryFull timeWork at officeLocal area
$24 - $38.5 per hour
...offers opportunities for learning about clinical research trials. It requires enthusiasm for... ...aspects of clinical trials, including coordinating necessary tests, procedures, and investigational... ...and audits to ensure compliance with regulatory requirements governing clinical...RegulatoryFull timeContract workWork experience placementLocal areaMonday to FridayShift workDay shift- ...growing team at Sarah Cannon Research Institute (SCRI), a... ...personalizing treatment. Through clinical excellence and cutting-edge... ...world.As the Clinical Research Coordinator you are responsible for overall... ...including enrollment, regulatory, quality, and site operations...RegulatoryFull time
- ...communities.Job Description Summary:The Clinical Consultant Research works in collaboration with the Principal Investigator (PI) to coordinate assigned clinical research studies in... ...position.Maintain familiarity with evolving regulatory and compliance context. Other duties as...RegulatoryFull timeLocal areaRemote workShift work
- ...world-renowned medical and research center, we strive to provide... ...with limited supervision, to coordinate research projects. This position... ...ensures quality control of clinical or basic research data in... ..., preparing and maintaining regulatory documentation and IRB submissions...RegulatoryFull timeLocal area
$22.25 - $36.38 per hour
...innovations in medical technology, research and family-friendly design. As the... ...study team in the implementation, coordination, and conduct of clinical research activities. Adheres to the... ...preparation and maintenance of all regulatory documents required by sponsors and...RegulatoryHourly payFull timePart time- ...and Sciences, has an exciting opportunity for a full time Clinical Research Coordinator 1 to work in Coral Gables, FL.The Department of... ...fundamental requirements of all international, national, and local regulatory bodies.Knows the contents and maintenance of study-...RegulatoryFull timeTemporary workWork at officeLocal area
- ...position, please review this tip sheet.The Clinical Translational Research Site is currently seeking a full-time Clinical Research Coordinator 1 to work in Miami.The Clinical... ...all international, national, and local regulatory bodies.Knows the contents and maintenance...RegulatoryFull timeTemporary workLocal areaWorldwideNight shiftWeekend workAfternoon shift
- DescriptionThe Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research... ...by the protocol.May assist in the preparation for regulatory agency site visits.Performs other related dutiesQualificationsBachelors...RegulatoryHourly payTraineeshipWork at officeLocal area
- DescriptionWe have an immediate opening for a Clinical Research Coordinator who will work with human specimens. The Clinical Research Coordinator... ...in the REDCap database.May assist in the preparation for regulatory agency site visits.Assists with IRB submissions.Other...RegulatoryHourly payTraineeshipWork at officeLocal areaImmediate start
- ...education, patient care, community service, research and technology development, and... ...SummaryThis position serves as a Clinical Research Coordinator in the Pediatric Critical Care Medicine... ...policies, and applicable regulatory requirements. The CRC Lead will work...RegulatoryFull timeRemote workMonday to FridayShift workWeekend work
- ...To support military mental health research, the full-time remote Clinical Research Coordinator II will review patient records, screen participants for eligibility... ...to ensure compliance with research protocols and regulatory requirements. Key responsibilities Reviews...RegulatoryFull timeLocal areaRemote work
- ...The University of Utah's Huntsman Cancer Institute seeks a Clinical Research Coordinator II to support study implementation, quality control, and... ..., enrollment monitoring, informed consent processes, regulatory submissions, staff supervision, and maintenance of study...Regulatory
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Regulatory Coordinator I. Be the first to apply!
- clinical research coordinator United States
- clinical research coordinator no experience United States
- entry level clinical research coordinator United States
- clinical project manager United States
- global clinical trial manager United States
- neuroscience clinical research coordinator United States
- clinical trials manager United States
- temporary clinical research coordinator United States
- clinical research coordinator ii United States
- clinical research study coordinator United States


