3,763 study manager jobs at 1,922 companies in United States
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Study Manager
Chandler or Tucson
OnsiteFull Time
StantecNYSE, TSX: STN: Global design, engineering, and consulting firm.
10+ YOE10+ years study/project management experience in mining or heavy industry; bachelor\u0002s in engineering preferred; PE preferred; strong leadership, risk/value management, communication, and stakeholder liaison skills.
StantecNYSE, TSX: STN: Global design, engineering, and consulting firm.
10+ YOE6+ MgmtLeads mining studies with 10+ years PM experience; strong leadership, risk management, stakeholder liaison; Bachelor's in Engineering; PE license preferred; MBA asset.
WorleyASX: WOR: Global provider of professional project and asset services.
10+ YOEBachelor's in engineering/mining/metallurgy or equivalent; 10+ years MMM industry experience and 8+ years ESP; experience leading front-end studies, NI 43-101/SK-1300 knowledge, strong analytical and stakeholder skills.
WorleyASX: WOR: Global provider of professional project and asset services.
10+ YOE8+ MgmtBachelor's in engineering or related,10+ years MMM industry experience,8+ years ESP experience,demonstrated front-end study leadership including OOM, PFS and FS,knowledge of NI 43-101/SK-1300,strong stakeholder and analytical skills.
CTI Clinical Trial and Consulting Services: Privately held global contract research organization serving pharmaceutical, biotechnology, and medical-device companies with clinical trials and consulting.
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
Altasciences: Private Canadian contract research organization serving pharmaceutical and biotechnology companies with integrated early drug development services.
High school diploma or GED and related experience required; college degree preferred. Requires strong written and verbal communication, leadership, organization, customer service, and fast-paced work skills.
Parexel: Global clinical research organization providing drug development services.
6+ YOEBachelor's degree with 7+ years or master's degree with 6+ years of operational clinical trial experience; study management leadership, CRO/vendor oversight, GCP knowledge, English fluency, and global travel availability required.
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.
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.
DM Clinical Research: Runs a network of clinical trial investigator sites.
5+ YOE5+ years clinical research experience required, knowledge of FDA and ICH-GCP, completion of study trainings, strong communication, and ability to manage site compliance and enrollment.
BeOne MedicinesNasdaq Global Select Market: ONC: Public Swiss oncology biopharmaceutical developing and delivering cancer medicines for patients worldwide.
8+ YOEBachelor's degree in a scientific or healthcare discipline, 8+ years of clinical research experience, and proven global clinical study project management experience. Advanced clinical operations knowledge required; oncology preferred.
Microsoft Office, Project Planning Applications, Clinical Trial Management Systems (CTMS)
NAMSA: Private global medical-device CRO serving MedTech companies with testing, preclinical and clinical research, and regulatory consulting.
3+ YOEBachelor's degree or equivalent experience, 3+ years of clinical trial or monitoring experience, project management experience, English fluency, GCP and medical device trial knowledge.
Electronic Data Capture (EDC), Clinical Trial Management System (CTMS), Trial Master File (TMF), Microsoft PowerPoint
iuvo Bioscience: Ophthalmology-focused contract research organization serving pharmaceutical, biotech, and medical-device companies with clinical trial services.
Bachelor's degree or equivalent, experience in clinical operations/drug-device development, ophthalmology experience preferred, knowledge of FDA/ICH/GCP/HIPAA/IRB, project management skills, strong communication and analytical abilities, Microsoft Office proficiency.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft Teams, SurveyMonkey, Microsoft Forms, EDC, eCRF
California Builder Services: California real-estate consulting firm helping developers and homeowner associations with public reports, budgets, and reserve studies.
Experience managing projects and staff, performing property inspections, preparing reserve study reports, client presentations, proficiency with Microsoft Word/Excel/Outlook, valid driver license and reliable transportation, ability to walk/stand/lift for inspections.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Bluebeam
Allergan AestheticsNYSE: ABBV: ’s medical aesthetics business develops, manufactures, and markets injectables, body-contouring, plastic-surgery, and skincare products for healthcare providers.
8+ YOEBachelor's degree required; 8+ years clinical research study management; leadership and cross-functional experience; experience with drug/device/interventional studies and end-to-end study operations; familiar with ICH/GCP and clinical trial systems (EDC, IRT, CTMS, eTMF).
TakedaTokyo Stock Exchange: 4502: Global research-driven biopharmaceutical.
6+ YOEBachelor's degree required, 6+ years in pharmaceutical or clinical research organizations, including 4+ years in clinical study management. Global and early- or late-phase study experience required.
Inspire Medical SystemsNYSE: INSP: Public medical technology developing and commercializing minimally invasive neurostimulation solutions for patients with obstructive sleep apnea.
5+ YOEManage clinical studies, oversee site selection/activation, track and report safety, collaborate with CROs/IRBs, and produce study documentation; bachelor\u0002s degree and 5+ years clinical research experience required.
Princeton or Miami or California or United Kingdom or Ireland
$139k-$163k/yrOnsiteFull Time
Summit TherapeuticsNasdaq: SMMT: Public biopharmaceutical oncology developing investigational medicines for patients with serious unmet medical needs.
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
Revolution MedicinesNASDAQ: RVMD: Clinical-stage oncology developing targeted RAS-addicted cancer therapies.
5+ YOEBachelor of Science in science and 5+ years of biotech, pharmaceutical, or CRO experience; knowledge of GLP, ICH, and FDA guidelines; strong collaboration, communication, prioritization, and deadline-management skills.
Oregon State University: Public land-grant research university based in Corvallis, Oregon.
3+ YOEBachelor's degree in relevant field, 3+ years progressive experience in international education or study abroad administration, student advising experience, cultural competency with Spain/Latin America, program coordination and budgeting skills, strong communication and analytical abilities.