Senior Clinical Research Coordinator — SoCRA Certified & GCP/IRB Oversight
Jefferson Health
Jefferson Health seeks a dedicated clinical research professional to oversee day-to-day trial activities in accordance with GCP. You will coordinate protocol activities, screen and enroll participants, manage data, and prepare regulatory documents for IRB reviews. The role involves training staff, developing workflows, and participating in cross-functional work groups to ensure compliant operations across multiple sites. #J-18808-Ljbffr Jefferson Health
- ...Overview Velocity Clinical Research is an owned and integrated... ...with the study protocol, GCP, and Velocity’s SOPs.... ...’s SOPs Implement and coordinate assigned clinical... ...documents to Sponsors and IRBs as required per... ...Coordinator through ACRP or SOCRA within six months of being...SeniorWork at officeFlexible hours
- Providence Health Plan Group is seeking a Clinical Research Coordinator to oversee daily operations of... ...Investigator, patients, sponsors, and the IRB to ensure timely and accurate documentation... ...strict adherence to study protocols (GCP/ICH). We value a background in medical...SuggestedWork at office
$110.7k - $200.9k
...United States Category: Clinical Trial Services Division... ...planning, conduct and oversight of the operational portion... ...procedures (SOPs), ICH-GCP and all applicable... ...Competent Authorities and IRB/Ethics Committees in... ...of 7 years of clinical research experience or proven competencies...SeniorContract workWork experience placementWork at officeLocal areaRemote workFlexible hoursNight shift- ...Clinical Research CoordinatorEvolution Research Group (ERG) is... ...The Clinical Research Coordinator is responsible for the... ...Good Clinical Practice (GCP), and company standard... ...studies with direct oversight from Site Director, and... ...Review Boards (IRBs) and other outside regulatory...SuggestedWork at office
- Cabaletta Bio is seeking an Associate Director, GCP Compliance to design and drive a risk-based QMS aligned with ICH GCP E6(R3). The role oversees documentation, training, vendor quality, and TMF health, enabling inspection readiness across GxP functions. This role can...SeniorRemote work
- ...Description M3 Wake Research, an M3USA Company,... ...sites meeting the clinical research needs of... ...today, our board-certified physicians have completed... ...Clinical Research Coordinator at Wake Research ,... ..., and high-level oversight of other clinical... ...completion of GCP Certification and...Flexible hours
$60k - $65k
Clinical Research Coordinator - Aesthetic Medicine Brian Biesman, M.D. | Nashville, Tennessee Full... ..., Good Clinical Practice (GCP), FDA regulations, IRB requirements, and site standard operating... ...training is a plus. ACRP or SOCRA certification is valued but not required...Full timeInternshipMonday to Friday- Position Clinical Research Coordinator II Purpose The purpose of the Clinical Research... ...the reporting of events to oversight agencies. Track enrollment... ...clinical research (CFR, GCP, HIPAA) Minimum 3 years of... ...including ICF process, role of the IRB and adverse event reporting...Work experience placement
- ## Senior Clinical Research Coordinator - PsychiatryApplyremote type: On Campus/Onsitelocations: Washington University Medical Campustime type: Full timeposted... ...documentation and reporting of adverse events; resolves IRB/protocol management issues and recommends corrective...SeniorWork experience placementWork at office
- ...to-end operational oversight and execution for... ...or more assigned clinical trials of moderate... ...functional teams, Clinical Research Organizations, and... ...the study level, coordinating Clinical... ...governance forums and senior stakeholders.... ...knowledge of ICH, GCP, and applicable global...SeniorWork at office
$140k - $175k
...Reporting to the VP of Clinical Operations, the Clinical Trial Manager (or Senior Manager) provides senior... ...planning, execution, oversight, and delivery of clinical... ...and compliance with GCP, ICH, protocol, and regulatory... ...vendors, and clinical research sites. Provides...SeniorFor contractorsWork at officeRemote work$160k - $170k
...develop their skills. The Sr. Clinical Trial Manager (Sr CTM) is... ...protocols, regulations and ICH/GCP. Track and manage monitoring report... ...metrics reporting. Assist in coordinating study specific training or re-... ...central laboratory, central IRB, central imaging, patient concierge...SeniorTemporary workWork experience placementWork at officeRemote workFlexible hours$50k - $52k
Clinical Research Coordinator Title: Clinical Research CoordinatorLocation: Frontage Clinical Services, Inc... ...with applicable regulations and GCP guidelines. Roles & Responsibilities:•... ...documents for review by the sponsors and IRB. Actively participate in any sponsor or...Contract workTemporary workImmediate start- ...treatments, ably supported by our Research department. We are an equal... ..., and compassionate Clinical Research Coordinator to join our team. The Clinical... ...compliance with FDA CFR, GCP and company SOPs. The CRC... ...Institutional Review Board (IRB) forms, processing updated...Private practiceWork at officeLocal area
- ## Clinical Research Coordinator 1Applylocations: LSU - Pennington Biomedicaltime type: Full timeposted on... ...study protocols, Good Clinical Practice (GCP), and regulatory requirements.* Travel... ..., and Institutional Review Board (IRB) requirements.* Experience using electronic...InternshipWork at officeFlexible hoursNight shift
$30 - $32.5 per hour
...ERA Health Research is seeking a full-time Clinical Research Coordinator I to join our Clinical Operations team in Redmond, WA. The Clinical Research... ...protocol and any protocol amendments according to GCP, verifying that only IRB/IEC approved versions of study documents are...Hourly payFull timeFlexible hours- ...-renowned medical and research center, we strive to provide... ...supervision, to coordinate research projects. This... ...quality control of clinical or basic research data... ...requirements.; ACRP or SOCRA certification a plus JOB... ...coordinator with oversight by PI. When outside of...Full time
$47.59k - $104.69k
## Clinical Research Coordinator 1Applyremote type: On Campuslocations: Pre-Clinical Science... ...with investigators and more senior study team members by... ...with Good Clinical Practice (GCP) guidelines.* Assist in the... ...hospital staff, physicians, IRB, review committees, clinical...Hourly payWork at office- Mallard Ridge Assisted Living, a community of Navion Senior Living, is seeking Certified Medication Technicians for medication administration-related... ...-quality medication administration and resident care oversight in a cutting-edge Assisted Living and Memory Care community...SeniorPart timeDay shift
- ...at Birmingham (UAB) Neurology Chair Office is seeking a Clinical Research Coordinator II to administer neuropsychological testing, manage data... ...participant recruitment, consent, and visit preparation under IRB and GCP guidelines. Ideal candidates hold a related bachelor’s...Work at office
$50.05k - $81.33k
Job Description - CLINICAL RESEARCH COORDINATOR II (T238715) CLINICAL RESEARCH COORDINATOR... ...accordance with the protocol, IRB regulations, and Good Clinical Practice (GCP). The mission of the UAB Alzheimer... ..., working with more senior team members to ensure compliance...Work experience placementWork at officeShift workDay shift- ...Hospital of Chicago is seeking a Clinical Research Assistant to support... ...study team in implementing and coordinating clinical research activities... ...with regulatory documents, IRB submissions, subject recruitment... ...with FDA, HSR, and GCP guidelines. #J-18808-Ljbffr...
$8,541 per month
...for an experienced Clinical Trial Manager (CTM... ...a global clinical research team supporting a... ...operational management and oversight of clinical trials... ...knowledge of ICH-GCP, clinical research... .... Experience coordinating CROs, vendors,... ...platforms. PMP, ACRP, SOCRA, or other relevant...Full timeWork at officeRemote work- Vanderbilt Health in Nashville is seeking a Clinical Translational Research Coordinator to support an early cancer-diagnosis study, coordinating... ...communication, strong teamwork, and meticulous regulatory oversight, including IRB submissions, trial documentation, and data quality...
$72.65k - $84.34k
Overview Clinical Research Coordinator Full-Time | Onsite | Monday - Friday $72,645.00 - $84,339 per year... ...reports, institutional review board (IRB) documents, and annual continuing review... ...sponsor monitoring visits preferred. SoCRA (CCRP) or ACRP certification preferred...Full timeWork experience placementWork at officeMonday to Friday$37.56 per hour
...its academic achievement, premier research, innovation and anteater mascot.... ...manage the regulatory lifecycle of clinical research studies, including study activation, IRB submissions, continuing reviews,... ..., Good Clinical Practice (GCP), IRB processes, and regulatory requirements...Temporary workPart timeLocal areaMonday to FridayAfternoon shift- South Shore Health System is seeking a Clinical Research Coordinator to support the clinical trials program onsite in Weymouth, MA. You will assist... ...and Research Manager. The role requires adherence to GCP, IRB protocols, and regulatory standards, with responsibilities...
$33.05 - $51.3 per hour
...the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple... ..., Patient, Sponsor, and the IRB. This position is directly responsible... ...strict compliance to study protocols (GCP/ICH). Providence caregivers are not simply...Minimum wageWork at officeLocal areaShift work- ...40 Position Summary Oversees and coordinates complex and multi-center clinical research studies and provides comprehensive... ...of the project(s). Provides oversight and coordinates complex and/or multi... .... (Optional Based on Department) SOCRA/ACRP certification. Preferred Qualifications...Work experience placementWork at office
$47.36k - $59.2k
Clinical Research Coordinator I, Department of Neurology Clinical Research Coordinator... ...direction of the PI and Senior lab members, assist with new... ...department for approval with oversight from supervisor. Provide... ...Arizona research policies, IRB processes, and industry and...Full timePart timeWork experience placementNight shiftWeekend work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Clinical Research Coordinator — SoCRA Certified & GCP/IRB Oversight. Be the first to apply!
- clinical research coordinator Brooklyn, NY
- clinical project manager Brooklyn, NY
- global clinical trial manager Brooklyn, NY
- neuroscience clinical research coordinator Brooklyn, NY
- clinical trials manager Brooklyn, NY
- clinical research coordinator ii Brooklyn, NY
- sr. clinical trial manager Brooklyn, NY
- clinical research coordinator remote Brooklyn, NY
- remote clinical trial manager Brooklyn, NY
- clinical project manager remote Brooklyn, NY

