56 Clinical Operations Management jobs in New York City.

New York City

• 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

Somerset

• Skills: clinical research, monitoring, study management, Good Clinical Practice, site management, data integrity, regulatory submissions, recruitment, documentation, communication
• Experience: Some organizations require completion of CRA training program or prior monitoring experience.
• Type: Full time

Somerset

• Skills: Human Resources, Clinical Research, Regulatory Affairs, Biopharmaceutical, Flexible Work Arrangement, Career Advancement, Inclusion, Diversity, Clinical Trials, Project Management

Jersey City

• 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

Basking Ridge

• Skills: medical director, clinical development, oncology, clinical trials, medical/scientific supervision, clinical study concepts, protocols, collaboration, scientific advisory boards, translational research
• Experience: 3 to 5 years
• Type: Contract

New York City

• Skills: clinical operations, clinical trials, CRO management, data integrity, regulatory guidelines, project management, leadership, strategy development, stakeholder communication, clinical study protocols
• Experience: 15+ years of clinical operations management experience
• Type: Full-time

Brooklyn

• Skills: Good Clinical Practices, clinical research, protocol compliance, patient recruitment, FDA regulations, ICH guidelines, data management, blood draws, patient coordination, documentation
• Experience: A minimum of 3 years prior Clinical Research Coordinator experience required
• Type: On-site

Basking Ridge

• Skills: Data Management, Clinical Data Management, CROs, Regulatory Requirements, Coaching, Mentoring, Performance Management, Project Budget, Data Quality, Risk Management
• Experience: Minimum of 8 years of clinical data management experience; Minimum of 3 years of people manager experience.
• Type: Contract

Jersey City

• Skills: clinical protocols, clinical study reports, investigator brochures, regulatory writing, document quality management, timelines, GCP guidelines, clinical development, project management, data interpretation
• Experience: 3+ years of relevant experience for Master's or 5+ years for Bachelor's degree.
• Type: Full-time

New York City

• Skills: clinical research, patient interaction, database management, research protocols, chemical exposure assessment, participant recruitment, clinical assessments, manuscript drafting, social media, healthcare
• Experience: 2 years of clinical research experience preferred

Jersey City

• Skills: clinical trials, mobile clinical services, research nurse, patient care, Good Clinical Practice, BLS Certification, travel requirements, nursing license, study participant visits, decentralized model
• Experience: Minimum 2+ years clinical/research experience preferred
• Type: Per Diem

New York City

• 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

Somerset

• Skills: preclinical development, project management, regulatory compliance, cross-functional teams, pharmaceutical, budget management, data management, IND programs, CRO management, communication skills
• Experience: At least 10 years of relevant work experience, including a minimum of 5-8 years of preclinical research, project management experience in pharmaceutical or biotech industry.
• Type: Full-time

Somerset

• Skills: Biotech, Project Leadership, Clinical Trials, Innovative Therapy, Patient Care, Research, Execution, Design, Milestones, Clinical Operations
• Type: Remote

Somerset

• Skills: Clinical Research Scientist, drug development, clinical trial protocols, patient recruitment, data management, regulatory documents, cross-functional teams, clinical studies, collaboration, Oncology Therapeutic Experience
• Experience: At least a Bachelor’s degree in life science discipline. Bachelor’s degree with 6+ years’; or MS with 5+ years’; or PharmD/PhD with 4+ years of pharma experience in clinical development or a related field.

New York City

• Skills: oncology, project management, clinical-stage, drug development, cross-functional, timelines, milestones, R&D functions, communication, process improvement
• Experience: 3+ years in drug development role, 2+ years project management experience in oncology
• Type: Full-time

Somerset

• Skills: Clinical Development Plan, Clinical trials, Good Clinical Practice, Regulatory authorities, IND, NDA/BLA, oncology, clinical strategy, management, collaboration
• Experience: 2 or more years of pharmaceutical experience in Clinical Development for Medical Director; 5 or more years for Senior Medical Director.
• Type: Full-time

New York City

• Skills: clinical trial execution, clinical study teams, vendor and CRO management, study budgets, data management, GCP regulations, study system setup, risk management, regulatory compliance, collaborative culture
• Experience: 7+ years in clinical operations, 3+ years in clinical project management within biotech, early phase oncology experience
• Type: Full-time

Princeton

• Skills: data management, vendor oversight, data quality, regulatory submissions, risk assessments, sponsor/vendor collaboration, clinical trial data, data standards, quality management, project management

New York City

• Skills: clinical trials, oncology, FDA, GCP, data review, clinical data, safety monitoring, protocol review, regulatory compliance, biotech
• Experience: Minimum of 5 years of highly relevant experience related to conduct of clinical trials
• Type: Full-time

New York City

• Skills: Clinical Data Management, CDM, Biopharmaceutical, EDC, Data Quality Reviews, Vendor Oversight, Clinical Trials, Data Processing, Biometrics, Project Management
• Type: full_time

Bridgewater

• Skills: clinical trial, regulatory submissions, data analysis, clinical protocol, biostatistics, GCP, ICH guidelines, FDA, EMA, scientific writing
• Type: full_time

Piscataway

• Skills: clinical trials, data entry, project manager, SOP adherence, observations recording, skin evaluations, test results, subject management, study protocol, data review
• Type: full_time