1mo
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Clinical Study Coordinator
Cleveland or Athens or Chattanooga
OnsiteFull Time
2+ YOE2+ years coordinating clinical research studies (or equivalent on-the-job training), GCP, IATA, and CPR required; phlebotomy and clinical research certification (ACRP/SOCRA) preferred; EDC data entry and site support experience.
EDC systems
3mo
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Clinical Nurse Study Coordinator
Cincinnati, Ohio, United States
OnsiteFull Time
Bachelor's degree and active RN license required. Perform/coordinate clinical procedures, administer medications, assess and document adverse events, screen/schedule subjects, and support study execution with Project Managers and Investigators.
1w
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Clinical Study Coordinator
Omaha, Nebraska, United States
$57k-$86k/yr OnsiteFull Time
2+ YOEBachelor's degree or equivalent, 2 years clinical or research experience, proficiency with Microsoft Excel/Word/Outlook, strong communication, organization, attention to detail, and computer literacy.
Microsoft Excel, Microsoft Word, Microsoft Outlook, Microsoft Access, EPIC One Chart
2w
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CLINICAL STUDY COORDINATOR
West Bend, Wisconsin, United States
$50k-$55k/yr OnsiteFull Time
1+ YOEAccredited college degree, 1+ year clinical research experience (or 2 years Phase I), BLS and ACLS (within first year), GCP knowledge, strong communication and organizational skills.
3w
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Clinical Study Coordinator
Austin, Texas, United States
$78k/yr OnsiteFull Time
3+ YOEBachelor's degree in a technical subject plus relevant experience (min 3 years) or advanced degree with experience; 1+ years clinical trials experience preferred; strong communication, organization, and Microsoft Office skills.
Microsoft Office
2w
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Study Coordinator
Chicago, Illinois, United States
$22-$26/hr OnsiteFull Time
Supports non-clinical toxicology studies under GLP: protocol generation, study coordination, documentation; BS in natural sciences required; GLP familiarity and study support experience preferred.
Provantis
1mo
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Clinical Nurse Study Coordinator
Cincinnati, Ohio, United States
OnsiteFull Time
Registered nurse with bachelor's degree; administer medications, assess subjects, perform procedures, work with study teams in Phase I clinical trials.
3mo
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Clinical Nurse Study Coordinator
Cincinnati, Ohio, United States
OnsiteFull Time
Bachelor's degree, nursing license (RN); clinical experience in acute care setting preferred.
1mo
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Study Coordinator - Freelance
San Diego, California, United States
OnsiteContract, Part Time
2+ YOE2+ years clinical research or healthcare experience; background as study coordinator/nurse or life sciences degree; knowledge of ICH-GCP and clinical trial processes; fluent English; proficient in MS Office; strong organization and communication skills.
Microsoft Office
1mo
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Clinical Study Coord
Duarte or Los Angeles or Orange County or Atlanta or Chicago or Phoenix
OnsiteFull Time
2+ YOEBachelor's in science/health preferred (substitutable by additional experience). Minimum 2 years research or clinical experience. Must obtain ACRP or SOCRA within 1 year; IATA, GCP, HSP, and BLS within 1 month. Understand/apply FDA, OHRP, GCP/ICH, HIPAA; execute protocols; coordinate recruitment/consent; monitor participants and report adverse even...
2mo
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Clinical Research Study Manager
Tomball, Texas, United States
OnsiteFull Time
5+ YOE1+ MgmtLead clinical study operations, ensure protocol compliance, data quality, training, and site coordination.
1mo
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Study Coordinator II
Honolulu, Hawaii, United States
$75k-$82k/yr OnsiteFull Time
6+ YOEBachelor's in biomedical science or nursing, 6+ years clinical/translational research experience (or 30+ studies), IRB/HRPP and regulatory compliance experience, data management and analysis skills, Microsoft Word/Excel and EMR proficiency, ability to pass background check.
Electronic Medical Records (EMR), Microsoft Word, Microsoft Excel
1mo
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Study Coordinator
Denver, Colorado, United States
$60k-$75k/yr OnsiteFull Time
3+ YOEAssociate's degree required (bachelor's preferred), minimum 3 years interventional trials research experience, ability to manage complex clinical protocols, significant computer work, must pass background check and non-federal drug test.
3d
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Research Study Coordinator
Chicago, Illinois, United States
$20-$25/hr OnsiteFull Time
2+ YOECoordinate clinical research activities, obtain consent, collect and analyze data, perform basic clinical procedures, complete IRB CITI training; bachelor's degree or equivalent and 2 years research experience required.
Microsoft Word, Microsoft Excel
1w
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Senior Study Coordinator
Bronx, New York, United States
$60k-$63k/yr OnsiteFull Time
1+ YOEBachelor's in public health or related field,1+ years clinical or community research experience,knowledge of human subjects/IRB,strong organizational and communication skills.
REDCap
1w
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Senior Study Coordinator
Bronx, New York, United States
$60k-$63k/yr RemoteFull Time
1+ YOEBachelor's degree,1–2 years clinical or community research experience,knowledge of human subjects/IRB,REDCap familiarity,strong organizational and communication skills,interest in AI or implementation science.
REDCap
2d
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Regional Study Coordinator - Central Labs Services - Clinical Research
Indianapolis, Indiana, United States
$60k-$65k/yr HybridFull Time
2+ YOEHigh school diploma,2+ years clinical research or laboratory experience; bachelor’s in life science preferred; strong communication, planning, and organizational skills; client-facing coordination experience.
1mo
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Research Study Coordinator II - Cancer Clinical - 40 Hours - Days
Detroit, Michigan, United States
OnsiteFull Time
1+ YOEBachelor's degree in a scientific or social science field, 1 year research coordination experience, interaction with study participants, regulatory compliance knowledge; SOCRA/ACRP and IATA certifications preferred.
1w
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Clinical Screening Coordinator
Rincon, Georgia, United States
OnsiteFull Time
Coordinating screening and assessment of participants for clinical trial studies at site level.
3w
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Study Coordinator - Research Professional 2
Minneapolis or Saint Paul
$26-$30/hr OnsiteFull Time
2+ YOEBA/BS plus ≥2 years research experience (or equivalent combo), experience with clinical interviews and consenting, ability to visit treatment sites, RedCap/Qualtrics data management, MRI coordination, strong communication and organization.
RedCap, Qualtrics
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