Madrigal PharmaceuticalsNASDAQ: MDGL: Develops and commercializes therapeutics for metabolic dysfunction-associated steatohepatitis.
1+ YOEBachelor's in life sciences or computer science; 1–2 years clinical data management or related experience; knowledge of GCP/ICH/FDA; experience with EDCs and MS Office; attention to detail and communication skills.
Medidata Rave, Oracle InForm, Veeva CDMS, Microsoft Excel, Microsoft Word, Microsoft PowerPoint, Microsoft Outlook
MedpaceNasdaq: MEDP: Full-service clinical contract research organization for medical development.
PharmD or PhD required; bachelor’s in life science noted; strong attention to detail, communication, Excel and Word proficiency; experience with research/statistical data preferred.
MedpaceNASDAQ: MEDP: Conducts clinical trials for biotechnology and pharmaceutical companies.
PharmD or PhD required; bachelor's in life science preferred. Experience with research/statistical data preferred. Strong attention to detail, communication skills, multitasking ability, and proficiency with Excel and Word.
Catholic Health: Provides comprehensive hospital and medical healthcare services.
5+ YOEActive NY RN license, BLS/CPR required, CPHQ preferred, 5+ years clinical nursing experience, performance improvement and data abstraction skills, EMR familiarity, strong communication and analytical ability.
Catholic Health: Integrated healthcare system providing hospital and clinical medical services.
5+ YOEActive NY RN license, BSN required; 5+ years clinical nursing experience; BLS/CPR/AED (AHA) required; CPHQ and master's preferred; data analytics, quality improvement, organizational and communication skills required.
Edetek: Develops digital platforms and data services for clinical research.
Ensures accuracy and reliability of clinical trial data through validation, reconciliation, reporting, coordination with study teams, and quality improvement.
Illume Fertility: Provides comprehensive fertility treatments and reproductive health services.
1+ YOEBachelor's degree in a related field, 1+ years administrative/project coordination or clinical research experience preferred, experience with IRB/regulatory documentation preferred, Microsoft Office proficiency, strong communication and organizational skills.
Yale University: Providing higher education and conducting advanced scientific research.
2+ YOETwo years of related work experience in the same job family and a Bachelor's degree in a related field; proficiency with Excel/Word and clinical data systems.
The START Center for Cancer Research: Global network of early-phase oncology clinical trial sites.
2+ YOEHigh school diploma/GED, 2 years clinical data entry experience, ability to collect/enter/review clinical data and coordinate monitor visits; familiarity with medical terminology preferred; CCRP/CCRC desirable.
Clinical Research Data Coordinator I- Winship Cancer Institute
Atlanta, Georgia, United States
OnsiteFull Time
Emory Healthcare: Academic healthcare system providing patient care and medical services.
1+ YOECoordinate and maintain clinical trial data, extract and enter data from medical records, support audits and monitoring, and ensure regulatory compliance. High school diploma/GED with 3 years admin experience OR alternative education/licensure pathways.
University of Nebraska Medical Center: Public academic health science center providing education and healthcare.
1+ YOEBachelor's in health science or related field (or equivalent experience), 1+ year data collection/management experience, knowledge of clinical research and records review, strong organization and communication skills.
Microsoft Excel, Microsoft Word, Microsoft Access, Microsoft PowerPoint, Microsoft Outlook
University of North Carolina at Chapel Hill: Public research university offering undergraduate and graduate degree programs.
Bachelor's degree or equivalent; coordinate and manage oncology clinical trial data, perform site initiation, ensure regulatory compliance with GCP and federal rules, navigate medical records and data extraction.
Senior Trauma Clinical Data Coordinator - Full Time - Day
Hackensack, New Jersey, United States
$35/hrOnsiteFull Time
Hackensack Meridian Health: Provides comprehensive medical care through a network of hospitals.
4+ YOEManage trauma clinical research data, perform chart abstraction, query resolution, EPIC and REDCap use, prepare regulatory submissions; BA in science/healthcare or 4+ years related experience; attention to detail and strong communication.
PubMed, REDCAP, EPIC, Business Intelligence (DTS), clinicaltrials.gov, Microsoft Office, Google Suite
UCSF Health: Academic medical center providing advanced patient care and research.
2+ YOEManage and coordinate clinical research studies, maintain regulatory compliance, handle data/specimens, support multi-center trials, and assist with grant preparation; requires HS or equivalent, research coordination experience, and CHR/clinical trial familiarity.
HCA HealthcareNYSE: HCA: Provides hospital and healthcare services through owned facilities.
1+ YOEBachelor's degree or 1+ year equivalent experience; coordinates research protocols, ensures informed consent and data integrity, tracks adverse events; Certified Clinical Research Coordinator preferred.
ALSAustralian Securities Exchange: ALQ: Provides global analytical testing and laboratory services for diverse industries.
Coordinate and execute clinical research studies in compliance with protocols and Good Clinical Practice; support data collection and study conduct under PI supervision. Must be eligible to work in the U.S.