23 study start up coordinator jobs at 11 companies in United States
2mo
Save
Mark Applied
Hide
Experienced Study Start-Up Coordinator
Cincinnati, Ohio, United States
OnsiteFull Time
1+ YOEBachelor's degree, 1+ years study coordinator/pharma start-up experience preferred, strong organization, attention to detail, Microsoft Office knowledge, excellent communication.
Trial Master File (TMF), Microsoft Office
3w
Save
Mark Applied
Hide
Study Start-Up Specialist
Chicago or Illinois
$55k-$70k/yr HybridFull Time
2+ YOEBachelor's in science/health,2+ years clinical research coordinator or CRO/pharma experience,knowledge of study start-up, FDA/GCP/HIPAA,project management,communication skills;CCRC preferred.
Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint
1w
Save
Mark Applied
Hide
Study Start-Up Coordinator (CRC Experience)
Cincinnati, Ohio, United States
OnsiteFull Time
1+ YOEBachelor's degree required, preferably in life sciences, plus 1–2 years of study coordinator or pharmaceutical industry experience. Requires strong organization, communication, and Microsoft Office knowledge.
Microsoft Office, Trial Master File (TMF), Institutional Review Boards (IRB)
1d
Save
Mark Applied
Hide
Experienced Study Start-Up Research Coordinator
Denver, Colorado, United States
$40k-$100k/yr HybridFull Time
3+ YOEBachelor's degree required, preferably in life sciences, plus 3+ years of clinical research coordinator or equivalent experience. Requires IRB submissions, informed consent development, Microsoft Office, organization, communication, and attention to detail.
Microsoft Office, Trial Master File (TMF)
3w
Save
Mark Applied
Hide
Clinical Research Regulatory & Study Start-Up Coordinator
Nashville, Tennessee, United States
OnsiteFull Time
1+ YOE1+ years clinical research or regulatory coordination experience; working knowledge of ICH E6(R2), FDA regulations, IRB submissions, eTMF/TMF maintenance, and HIPAA; Microsoft Office proficiency; familiarity with CRIO/Redcap/CTMS preferred.
CRIO, Redcap, CTMS, eTMF, Microsoft Word, Microsoft Excel, Microsoft Outlook
1mo
Save
Mark Applied
Hide
Clinical Research Coordinator (Nephrology)
Baltimore, Maryland, United States
$17-$30/hr OnsiteFull Time
Coordinate clinical study activities, support study start-up and IRB submissions, recruit and consent participants, manage data entry, and liaise with investigators and regulatory bodies.
1w
Save
Mark Applied
Hide
Participant Marketing Coordinator
Lake Worth or United States or Canada
$68k-$78k/yr RemoteFull Time
2+ YOEBachelor's degree preferred and 2–5 years of project coordination, marketing operations, clinical research, or healthcare administration experience; study start-up, sponsor budgets, and vendor management preferred.
IRB, EC, CROs
3w
Save
Mark Applied
Hide
Clinical Research Coordinator
Chicago, Illinois, United States
OnsiteFull Time
3+ YOE3+ years clinical research coordination experience preferred; bachelor's in life sciences/nursing/healthcare preferred; experience with study start-up, regulatory submissions, EDC and MS Office; strong communication and organizational skills.
Electronic Data Capture (EDC), Microsoft Office
3w
Save
Mark Applied
Hide
Regulatory Coordinator II
Seattle, Washington, United States
$80k-$104k/yr HybridFull Time
2+ YOEPrepare and maintain regulatory documentation, submit to IRB/FDA/sponsors, conduct audits, support study start-up and close-out, and ensure GCP and institutional compliance.
SharePoint, Florence, OneDrive, OnCore, Microsoft Office
3w
Save
Mark Applied
Hide
Clinical Research Coordinator IV, Department of Internal Medicine – Cardiology (Phoenix)
Phoenix, Arizona, United States
$66k-$85k/yr OnsiteFull Time
8+ YOEBachelor's degree and 8+ years related experience; responsible for study start-up, coordination, regulatory compliance, enrollment, data submission, and mentoring staff.
1mo
Save
Mark Applied
Hide
Regulatory Coordinator II - Clinical Trial Office
Brookline or Maine or Vermont or New Hampshire or Massachusetts or Connecticut or Rhode Island
$61k-$68k/yr HybridFull Time
1+ YOECompletes regulatory submissions and tracking for clinical trials (IND/IDE, IRB, FDA), maintains regulatory files, coordinates study start-up, and ensures compliance with FDA and ICH/GCP; requires bachelor’s degree or equivalent experience and 1–3 years regulatory experience.
Microsoft applications, databases
1mo
Save
Mark Applied
Hide
Clinical Research Coordinator Manager - Oncology
Cerritos, California, United States
$80k-$87k/yr OnsiteFull Time
6+ YOEOversee CRCs and RAs for oncology trials; ensure ICH-GCP/FDA/HIPAA compliance; manage study start-up, regulatory submissions, data quality, and budgets. Bachelor's preferred; CCRC and phlebotomy desired; 6+ years clinical research experience.
eSource, EDC
1mo
Save
Mark Applied
Hide
UNIV - Regulatory and Grant Administration Coordinator - Department of Dermatology
Charleston, South Carolina, United States
$45k-$77k/yr OnsiteFull Time
3+ YOEBachelor's degree and 3 years relevant experience; experience with study start-up, IRB submissions, grant budgets, Cayuse, SPARC, EPIC, eReg systems, ClinicalTrials.gov, and regulatory compliance.
SPARC, EPIC, Cayuse, eReg, ClinicalTrials.gov
Explore Jobs