39 Clinical Operations Management jobs in Boston.

Cambridge

• Skills: clinical research finance, invoicing, accounts payable, clinical research budgets, Clinical Trials Management System, RealTime, study budgets, financial reports, GAAP principles, stakeholder communication
• Experience: At least 7 years’ experience working with clinical research finance, for a research site; 5+ years experience in a strategic customer facing role
• Type: Full-time

Boston

• Skills: clinical trials, go-to-market strategies, sponsor-site interactions, contract research organizations (CROs), site collaboration, adoption, Site Connect application, efficiency, clinical operations, cross-functional team
• Experience: Strong understanding of clinical operations and sponsor-site interactions
• Type: Full-time

Cambridge

• Skills: data annotation, machine learning, cross-functional, project management, annotation teams, clinical research, regulatory submissions, quality metrics, dynamically-paced environment, Gastroenterology
• Experience: Over 2 years of experience in data annotation, data operations, or related fields, including at least 1 year in leading annotation teams.

Boston

• Skills: data management, clinical data management, project management, negotiations, quality management, financial tracking, process improvements, Good Clinical Practices, regulatory guidelines, compliance
• Experience: 5 years direct Data Management experience, including 3 or more years as a CDM project lead.
• Type: Full time

Cambridge

• Skills: leadership, clinical operations, clinical trial, obesity, metabolism, global management, cross-functional, strategic direction, project management, GCP
• Experience: 15+ years of clinical operations experience
• Type: Contract

Boston

• Skills: Program Management, Drug Development, Project Management, Biotechnology, Collaboration, Clinical Trials, IND Preparation, Partnerships, Project Plans, Communication
• Experience: Program management experience for drug development programs in late nonclinical/early clinical phases, with proven track record of advancing candidates into the clinic.

Boston

• Skills: clinical trial, stakeholder management, CRO oversight, GCP, ICH guidelines, clinical trial methodology, budget management, risk management, cross-functional team, vendor management
• Experience: 8+ years
• Type: Full-time

Cambridge

• Skills: Clinical Trial Design, Clinical Trials, Phase I, Phase II, Medical Monitoring, Safety Oversight, Regulatory Requirements, Compliance, Clinical Strategy, Cross-functional Team
• Experience: A minimum of 6 years of industry experience in clinical development in a pharmaceutical or biotech company setting.
• Type: Full-time

Cambridge

• Skills: clinical trial management, leadership, strategic management, clinical operations, quality, timelines, budgets, risk mitigation, vendor management, staff recruitment
• Experience: Minimum of 12 years relevant sponsor side pharmaceutical industry experience, 8 years within clinical trial management.
• Type: On-site/Hybrid

Boston

• Skills: clinical studies, CRO management, Informed Consent Form, project leadership, timelines, budgets, site management, quality assurance, clinical trial communications, CNS therapeutic experience
• Experience: Minimum 4+ years of experience or demonstration of equivalent capability in a Clinical Trials Manager role
• Type: Hybrid

Boston

• Skills: market research, healthcare, biological sciences, expert network, project management, scheduling, communication, consulting, expertise, compliance
• Experience: Minimum of 1-2 years' work experience in a healthcare-related field or life sciences firm.
• Type: Full-time

Cambridge

• Skills: clinical trials, study design, project management, budget management, protocol development, regulatory compliance, risk assessment, vendor management, cross-functional leadership, data quality
• Experience: Minimum of 8 years of relevant industry experience
• Type: Full-time

Watertown

• Skills: Clinical Development Planning, Clinical Development Implementation, Clinical trial protocols, Oncology, Medical monitor, Good Clinical Practice, Biostatistics, Translational Biomarker, Regulatory interactions, Ethical conduct
• Experience: Clinical practice experience ≥ 4 years.
• Type: Full-time

Somerville

• Skills: clinical operations, clinical trial management, global clinical trials, cross-functional teams, ICH/GCP guidelines, regulatory guidelines, risk management, project management, budget management, patient recruitment
• Experience: 8+ years of clinical operations experience, including 4+ years as a clinical trial manager
• Type: Full-time

Boston

• Skills: clinical research, operations management, study deliverables, project management, clinical trials, talent development, team leadership, regulatory compliance, performance metrics, stakeholder management
• Experience: Minimum 7 years of clinical research experience

Waltham

• Skills: Clinical Operations, clinical trials, study conduct, regulatory documents, study metrics, team collaboration, investigator meetings, trial master file, best practices, inspection readiness
• Experience: 2+ years of relevant hands-on drug development experience in Sponsor setting
• Type: Full-time

Cambridge

• Skills: Clinical Development, Neuroscience, Medical Monitoring, Regulatory Affairs, Clinical Trials, Strategic Decision Making, Cross-functional Teams, Adverse Events, Pharmaceutical Development, Patient-Focused
• Experience: MD (or equivalent) in relevant area with appropriate post-doctoral training and certification
• Type: Hybrid

Waltham

• Skills: Program Management, Cross-functional team, Development plan, Clinical development, Regulatory strategy, Project execution, Stakeholder communication, Risk management, Neuromuscular diseases, Therapeutics
• Experience: 8-12+ years

Boston

• Skills: clinical trial finance, budgeting, forecasting, vendor invoices, financial trackers, accrual reports, contract negotiations, study budgets, financial summaries, ERP systems
• Experience: 5+ years in clinical trial finance or operations
• Type: Contract

Cambridge

• Skills: T-cell engagers, clinical trials, project management, regulatory requirements, vendor oversight, CRO management, clinical operations, clinical development, Immunology, mAb therapeutics
• Type: full_time

Boston

• Skills: pharmacovigilance, patient safety, regulatory compliance, gene therapy, clinical development, risk assessment, post-marketing surveillance, international regulatory requirements, high-performing teams, collaboration
• Type: full_time

Boston

• Skills: clinical trials, regulatory documents, TMF management, CRO oversight, audit and inspection readiness, patient-focused, drug development, project timelines, budget management, clinical research
• Type: full_time

Waltham

• Skills: clinical operations, vendor management, budget management, clinical trials, strategic plans, cross-functional teams, GCP guidelines, negotiation, process improvements, operational efficiencies
• Type: full_time

Cambridge

• Skills: clinical trial, Trial Master Files, CROs, clinical studies, Study Team Leader, study supplies, meeting minutes, benchmark metrics, proprietary capabilities, clinical project teams
• Type: contract

Woburn

• Skills: clinical development, Good Clinical Practices, regulatory submissions, clinical trials, interventional radiology, medical expertise, CRO, budget management, patient outcomes, cross functional collaboration
• Type: full_time

Boston

• Skills: administrative tasks, scientific tasks, medical communications, project coordination, healthcare sector, quality control, client communication, project compliance, team collaboration, data extraction
• Type: full_time

Boston

• Skills: neuromonitoring, clinical strategy, clinical trials, regulatory requirements, medical devices, critical care, study design, clinical research, neuroscience, startup environment
• Type: full_time

Cambridge

• Skills: project management, biotech, pharmaceutical, IND submission, platform-based, communication, risk mitigation, data analysis, cross-functional teams, MIMIC platform
• Type: full_time

Cambridge

• Skills: clinical development, early-phase clinical trials, protocol development, clinical trial management, regulatory compliance, data management, biostatistics, pharmacology, clinical strategy, vendor management
• Type: full_time

Cambridge

• Skills: clinical pharmacology, oncology, autoimmune disease, clinical development, study protocols, regulatory documents, therapeutics, biopharmaceutical, CROs, translational medicine

Boston

• Skills: clinical trial management, IND submission, vendor management, project management, clinical operations, cross-functional teams, GCP, ICH, oncology, synthetic lethality
• Type: full_time

Cambridge

• Skills: Clinical Research, Biostatistics, Regulatory Affairs, Data Management, Statistical Programming, Project Leadership, Patient Care, Clinical Trials, Remote Work, Employee Well-being
• Type: full_time

Boston

• Skills: clinical trials, patient recruitment, regulatory compliance, Good Clinical Practice, data management, adverse events, drug development, clinical trial management system, study coordination, study documentation
• Type: full_time