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
$21.16 - $35.29 per hour
...Job Overview The Clinical Research Coordinator II (CRC II) is a... ...studies, under the oversight of the Principal... ...sponsors, CROs, and IRBs. Requirements and... ...Practice (ICH GCP). Strong organizational... ...System). Certified clinical research certification (SoCRA or ACRP) preferred...SuggestedHourly payWork at office- ...available within our clinical research department. If you... ...Clinical Research Coordinator will be... ...Clinical Practice (GCP) guidelines. Safety... ...the sponsor and the IRB. Individuals may... ...Certifications/Licensures: (Certified Clinical Research... ...(CCRP-SoCRA)) EXPERIENCE Previous...SuggestedLocal areaShift work
- ...achievement, premier research, innovation and... ...UCI Center for Clinical Research (CCR)... ...as primary coordinator on trials of... ...for review and oversight of clinical trials... ...Practice (GCP)/ International... ...Review Board (IRB), Food and Drug... ...certification through SOCRA or ACRP Special...SuggestedWork experience placementWork at officeLocal area
- Flourish Research's Valkyrie Clinical Trials Denver site is actively hiring a Clinical Research Coordinator to support study visits, data collection, and patient care in oncology... ...obtaining informed consent, adhering to GCP/IRB, and mentoring junior staff. This onsite...SeniorDay shift
- Clinical Research Coordinator - SR Responsibilities Works independently or with minimal... ...Clinical Research Practice (GCP). Runs portions of clinical... ...visits, and regulatory and/or IRB document preparation.... ...School Diploma or equivalent and SoCRA certification and 6 years of...SeniorDaily paidFull timeTemporary workPart timeFlexible hoursShift work
- ...and agile execution. Our clinical development footprint covers... ...than 100 professionals across research, development, regulatory, and... ...management with strategic oversight in a highly collaborative, entrepreneurial... ..., and in compliance with GCP and regulatory standards....SeniorContract workWork at officeLocal areaRemote work
- ## Senior Clinical Project ManagerApply: US - Remote: Full... ...contact to Contract Research Organizations (CROs),... ...conductivity follows ICH-GCP, FDA/EMA, or other... ...study, in particular, oversight of CRO activities... ...Responsible for leading and coordinating the development of...SeniorFull timeContract workFor contractorsLocal areaRemote work
$52k
...Department Massey Clinical Trials Office Department... ..., cutting-edge research; person-centered... ...Clinical Research Coordinators support Principal... ...Practice (GCP), and additional certifications... ...and adhere to all IRB requirements,... ...Associates (SOCRA), the Association...Full timeTemporary workWork at officeRemote workFlexible hours- Description Clinical Research Coordinator (CRC) The Clinical Research Coordinator (CRC... ...process. Clinical Oversight & Subject Monitoring Monitor... ...issues to the PI, sponsor, and IRB as required. Documentation... ...activities comply with SOPs, GCP, and regulatory...Work at office
$60.84k - $98.86k
Job Description - CLINICAL RESEARCH COORDINATOR III (T240021) CLINICAL... ...coordinator by providing oversight to less experienced... ...Clinical Practice (GCP). Key Duties &... ...education requirement. Certified Clinical Research... ...Vice President and Senior Title IX Coordinator...Work experience placementShift workDay shift- ...primary responsibility of the Clinical Research Coordinator III is to coordinate and... ...adverse event reporting, and IRB regulatory files.... ...Qualification: Certification as a Certified Clinical Research Coordinator... ...Research Associates or SoCRA) is strongly desired Supervisory...Full timeWork experience placementWork at officeLocal area
- ...we lead in education, research, health care delivery... ...PI) or designee, the Clinical Research Coordinator is responsible for... ...accordance with the IRB approved protocols and... ...Good Clinical Practice (GCP) guidelines and all... ...will provide day-to-day oversight and coordination of...Work at officeLocal area
$31.83 - $47.73 per hour
...and groundbreaking research focused on cancer... ...Hutch operates eight clinical care sites that... ...Clinical Research Coordinator ensures all administrative... ..., regulatory and GCP guidelines, and... ...preferred. Certified Clinical Research... ...Research Professional (SOCRA). Minimum five...Hourly payH1bRemote workVisa sponsorshipFlexible hours$56.2k - $81.5k
...motivated and detail-oriented Clinical Research Coordinator (CRC) to support a diverse... ...effective coordination and oversight of clinical research... ...policies, Good Clinical Practice (GCP), and applicable federal... ...compliance documentation (e.g., IRB, Clinical Trials Office)*...Full timeWork experience placementWork at officeRemote work- ...alternative application process. Clinical Research Coordinator Atascocita, TX, US 10 days... ...(e.g., ACRP‑CRC or SOCRA). Experience working with electronic... ...Institutional Review Board (IRB) processes. Previous... ...and Good Clinical Practice (GCP) guidelines throughout the study...
- ...quality dermatology clinics that focus on... ...communicating and coordinating work efforts with... ...of clinical trial research studies based upon... ...Director, sponsor and IRB of any serious adverse... ...accordance with GCP, ICH and FDA... ...related to research.* Certified Clinical Research...Temporary workWork at office
- ...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
- University of Pennsylvania is seeking a Clinical Research Coordinator B to conduct in-home and on-site study visits, manage IRB submissions, and provide administrative support for research operations. The role includes coordinating documentation, literature reviews, and...
- ...Angeles is seeking a data-driven professional to collect data for clinical trials independently and prepare study documentation for regulatory review, including IRB submissions. You will support clinical research activities and lab operations, ensure timely documentation,...Senior
- ...Medical Center is seeking a detail-oriented Research Coordinator to assist in coordinating patient participation and data collection for clinical studies in a supportive academic setting.... ...will handle regulatory documentation, IRB submissions, and scheduling, while ensuring...Senior
- Tulane University is seeking a Clinical Research Coordinator III to coordinate and conduct all aspects of a clinical study with minimal supervision.... ...liaising between patients, investigators, collaborators, and the IRB, and assist with protocol development and SOPs. #J-18808-...Senior
$26.78 per hour
## Senior Clinical Research CoordinatorApply: Onsite: 32 Fruit Street Boston (Yawkey Center): Boston... ...**The Senior Clinical Research Coordinator (Sr. CRC) works independently under minimal... ...· Scans in research documents and certifies these documents as copies Skills/Abilities...SeniorFull timeWork at officeRemote workShift 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$164k - $214k
The Senior Clinical Trial Manager will lead, manage and co-ordinate... ...accordance with ICH-GCP and applicable local... ...MA office. Lead and coordinate a cross-functional... ...plans including; vendor oversight, risk, quality, safety... ...knowledge and clinical research best practices....SeniorWork at officeLocal areaRelocation package$158k - $185k
...lives through Summit’s clinical studies in the field of... .... Overview of Role The Senior Clinical Trial Manager (... ...leadership and operational oversight of complex global clinical trials coordinates, while leading and... ...process, ICH guidelines/GCP with a deep understanding...SeniorContract workFor contractorsFor subcontractorWork at office- Georgetown University seeks a Clinical Research Coordinator II to lead coordination on surgical service studies, under PI supervision. You will handle... ..., with solid knowledge of FDA/OHRP regulations and ICH GCP. On-campus work arrangement is specified, with competitive...Senior
$21 - $35.54 per hour
## Clinical Research Coordinator II (Non-RN)Apply: US-VA-Fredericksburg: Full time:... ...protocols in accordance with GCP, ICH/FDA guidelines and... ...investigational product, investigator oversight, reporting and following up... ...**** Understanding of the IRB/IEC review, key elements of...Full timeContract workRemote workMonday to Friday$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$130k - $170k
...application process. Clinical Trial Manager / Senior Clinical Trial... ...lock and closeout, coordinate internal and external... ...Coordinate sponsor oversight of monitoring activities... ...progressive clinical research experience, including... ...knowledge of ICH-GCP, applicable FDA and...SeniorFull timeWork at officeLocal areaRemote workShift work- ...injury (SCI). We are seeking a Clinical Research Coordinator II to serve as the operational... ...session equipment cleanup Regulatory Oversight and Compliance Prepare and submit IRB applications, amendments, and... ...and certifications (CITI, GCP, BLS) Perform other duties as assigned...TraineeshipWork experience placementWork at office
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