50 study start up manager jobs at 33 companies in United States
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Sr. Manager, Study Start Up
Cambridge or Boston
$140k-$190k/yr RemoteFull Time
8+ YOE5+ MgmtBachelor's degree in science or related field, 8+ years in multinational clinical studies, 5+ years managing clinical study operations, and global study start-up, site activation, CRO, GCP, and regulatory experience.
Key Performance Indicators (KPIs)
2w
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Sr. Manager, Study Start Up
United States
$140k-$190k/yr RemoteFull Time
8+ YOE5+ MgmtBachelor’s degree in science or related discipline; 8+ years in multinational clinical studies, 5+ years managing clinical study operations, global study start-up leadership, CRO collaboration, GCP knowledge, and regulatory understanding.
6d
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Manager Study Start Up
Princeton or Miami or California or United Kingdom or Ireland
$139k-$163k/yr OnsiteFull Time
5+ YOERequires 5–7 years of feasibility, study start-up, site agreements, and eTMF experience in biotechnology or pharmaceuticals, plus global trial knowledge, ICH/GCP expertise, negotiation, budgeting, and cross-functional communication skills.
Microsoft Office, Microsoft Word, Microsoft Excel, electronic document management systems, document review tools, grant plan
1w
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Study Start Up Manager
United States
$120k-$181k/yr OnsiteFull Time
3+ YOEBachelor's degree and 3+ years of clinical study start-up leadership, 1+ year of hands-on Veeva Vault experience, informed consent review and language negotiation experience, and strong project management and communication skills.
Veeva Vault, Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF), electronic Investigator Site File (eISF)
1w
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Study Start Up Manager
Wilmington, Delaware, United States
$120k-$181k/yr OnsiteFull Time
3+ YOEBachelor's degree, 3+ years of clinical study start-up leadership, 1+ year of Veeva Vault experience, informed consent and language negotiation experience, ICH-GCP knowledge, and strong project, communication, organizational, and negotiation skills.
Veeva Vault, CTMS, eTMF, eISF
1w
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Study Start Up Manager
Wilmington, Delaware, United States
$120k-$181k/yr OnsiteFull Time
3+ YOEBachelor's degree and 3+ years of clinical study start-up leadership, including 3+ years of informed consent review and language negotiation plus 1+ year of Veeva Vault experience; knowledge of ICH-GCP and clinical trials required.
Veeva Vault, CTMS, eTMF, eISF
2mo
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Study Start-Up Project Manager
Cincinnati, Ohio, United States
OnsiteFull Time
5+ YOEBachelor's required (advanced degree preferred),5+ years clinical research experience, project management and leadership in study start-up, cardiovascular/metabolic experience desired, strong communication skills.
1w
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Study Start-Up (SSU) Manager (4145)
Houston, Texas, United States
OnsiteFull Time
5+ YOERequires 5+ years of clinical research experience, 3+ years in study startup or related operations, and experience managing timelines, milestones, cross-functional workflows, and concurrent studies.
Clinical Trial Management System (CTMS), Microsoft Office Suite, Microsoft Google Workspace
1mo
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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
2w
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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)
1w
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Study Start Up Lead Contractor
Boston, Massachusetts, United States
RemotePart Time, Contract
8+ YOEBA/BS and 8+ years supporting or independently managing global clinical trials; strong ICH/GCP, regulatory, drug development, CRO/vendor oversight, communication, and cross-functional collaboration experience.
1mo
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SCI-CTO Study Start-UP Project Manager (Hybrid)
Stanford, California, United States
$86k-$100k/yr HybridFull Time
2+ YOEBachelor's degree and 2 years clinical research experience; knowledge of clinical trials data management, regulatory requirements (HIPAA,FDA,IRB,GCP), medical terminology, Microsoft Office; supervisory experience.
Microsoft Office
2w
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Study Start-up and Regulatory Manager
North Carolina, United States
HybridFull Time
3+ YOEBachelor's degree and 3+ years independently managing IRB submissions, essential document collection, and TMF maintenance; knowledge of ICH-GCP, FDA regulations, and IRB/IEC requirements required.
Trial Master File (TMF)
1mo
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Manager Study Start-up
Aliso Viejo or San Clemente or Burlington or United States
$130k-$163k/yr OnsiteFull Time
8+ YOE8+ years clinical research experience in medical device/pharma; experience leading study execution, timelines, budgets, and cross-functional teams; strong knowledge of FDA regulations and GCP; risk management skills.
2w
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Study Activation Manager
Raleigh, North Carolina, United States
HybridFull Time
8+ YOEBachelor's degree in science, healthcare, or related field or equivalent experience; 8 years of clinical research experience with significant study start-up, site activation, clinical operations, or trial management experience.
clinical trial management systems, start-up tracking tools, Microsoft Teams
1mo
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UNIV - SISU Start-Up Manager & Protocol Writer - Hollings Cancer Center
Charleston, South Carolina, United States
$66k-$120k/yr OnsiteFull Time
3+ YOEBachelor's degree and 3+ years relevant experience; knowledge of GCP, CFR, FDA/IRB processes; protocol writing, study start-up, regulatory submissions, and clinical trials systems.
OnCore, eReg, clinicaltrials.gov
1mo
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Sr Clinical Study Manager
San Diego or United States
$150k-$190k/yr RemoteFull Time
6+ YOEBachelor's or master's in science/healthcare required, 6+ years clinical trial management, CRO/vendor management, budget and site oversight, trial start-to-finish experience, travel up to 25%, intermediate-advanced Excel/PowerPoint.
Microsoft Excel, Microsoft PowerPoint
1mo
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Entry-Level Project Coordinator (Study Start-Up)
Cincinnati, Ohio, United States
OnsiteFull Time
Bachelor's degree required (life sciences preferred), office experience preferred, strong organization and prioritization, Microsoft Office knowledge, attention to detail, excellent oral and written communication.
Trial Master File (TMF), Microsoft Office
2mo
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Local Study Associate Director- FSP
United States or North Carolina
RemoteFull Time
3+ YOEOncology-experienced LSAD (cell therapy preferred) with 3+ years in Development Operations (CRA/SrCRA). Leads local study teams, manages site start-up/monitoring, ensures ICH-GCP compliance, bachelor's preferred, national/international travel required.
CTMS, eTMF
1mo
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Site Recruiter - Feasibility & Start-up With CorEvitas
Waltham, Massachusetts, United States
$83k-$125k/yr RemoteFull Time
5+ YOEBachelor's preferred; minimum 5 years clinical research/site start-up experience; experience identifying investigator sites, site activation, feasibility, and study start-up; strong analytical, communication, and project management skills.
Salesforce, CTMS, ClinicalTrials.gov
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