56 Clinical Operations Management jobs in San Francisco.

Redwood City

• Skills: Clinical Quality, GCP, audit plans, regulatory standards, clinical trials, biotechnology, risk assessment, communication skills, compliance guidance, training development
• Experience: 8+ years’ experience working within GCP in a pharmaceutical or biologics environment.
• Type: Full-time
• Salary: $135,000 - $155,000

Palo Alto

• Skills: Pharmacovigilance, Drug Safety, Individual Case Safety Reports (ICSRs), FDA safety regulations, ICH Guidelines, Adverse events, Study Management Teams (SMTs), Safety Management Plan (SMPs), Training documents (SOPs), Market Research and Patient Support programs (MAPs)
• Experience: Minimum of 8 years recent experience in Pharmacovigilance required; relevant pharmaceutical industry experience in drug safety required.

Fremont

• Skills: clinical trials, Clinical Research Associate, GCP, FDA, ICH guidelines, monitoring, regulatory compliance, patient recruitment, medical device studies, data capture systems
• Experience: Minimum of 5 years of experience working in clinical trials with 3 years as a Clinical Research Associate
• Type: Full-time
• Salary: $89,000 — $148,000 USD

San Francisco

• Skills: clinical trial management, project timeline adherence, quality delivery, clinical research, monitoring, regulatory documentation, data cleaning, collaborative environment, communication skills, clinical trial activities
• Experience: 5-7 years of clinical research experience with significant clinical monitoring experience.
• Type: Full-time

Redwood City

• Skills: data management, clinical studies, database activities, protocol review, data integrity, data cleaning, oncology, Medidata RAVE, regulatory guidelines, communication skills
• Experience: Minimum of 7 years of clinical data management experience in the pharmaceutical, biotechnology industry or in a CRO.
• Type: Full-time
• Salary: $180,000 - $195,000 per year

Alameda

• Skills: external data management, clinical trials, data quality, biological samples, FDA regulations, project management, oncology, vendor management, electronic data capture, data transfer plan
• Experience: Minimum of 11 years of related experience
• Type: Full-time
• Salary: $181,500 - $257,500 annually

San Rafael

• Skills: Medical Writing, Clinical Studies, Submissions, Document Preparation, Protocols, Informed Consent Forms, Safety Reports, Regulatory Submissions, Documentation Management, Biotechnology
• Experience: At least 5 years experience required
• Type: Contract
• Salary: null to null per hour

San Francisco

• 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
• Salary: $82,300.00 - $173,900.00

Sunnyvale

• Skills: clinical studies, evidence generation, clinical protocols, project management, regulatory compliance, biostatistics, clinical research, data analysis, stakeholder engagement, medical device trials
• Experience: Minimum Advanced degree in a scientific/bioengineering field (M.S., Ph.D. or M.D.) with a minimum of 5 years of experience in clinical research, or Bachelor’s degree in a scientific/bioengineering field with a minimum of 8 years of experience in clinical research is preferred, or a minimum of 10 years of experience in clinical research with relevant training.
• Type: Clinical & Medical Affairs

Fremont

• Skills: clinical trials, clinical studies, Good Clinical Practice, compliance, medical devices, ISO14155, communication, project management, neuroscience, regulatory requirements
• Experience: 5+ years of academic or industry experience working with medical devices
• Type: Full-time
• Salary: $105,000 - $195,000 USD

Santa Clara

• Skills: clinical research, project management, clinical trial, vendors, regulatory standards, protocol compliance, data collection, investigational sites, study design, clinical data
• Experience: Minimum 10 years’ experience directly supporting clinical research
• Type: Full-time

Newark

• Skills: clinical trials, study trackers, data verification, SOPs, clinical operations, protocol design, ICH/GCP regulations, teamwork, communication skills, Microsoft applications
• Experience: 2+ years in Clinical operations or healthcare-related experience
• Type: Full-time
• Salary: $85,000-$103,000

San Rafael

• Skills: Regulatory Affairs, CMC, Pharmaceutical, Biotechnology, Global Regulatory Strategy, Clinical Trials, Marketing Applications, Risk Assessment, Manufacturing Changes, Cross-functional Teams
• Experience: At least 12-15 years of experience in Regulatory Affairs CMC or related discipline in the pharmaceutical or biotechnology industry

Palo Alto

• Skills: clinical studies, Good Clinical Practice (GCP), Trial Master File (TMF), monitoring, site management, regulatory submissions, data entry, quality reviews, clinical trial documentation, problem-solving
• Experience: Minimum 4-6 years of experience within clinical operations, study coordinator, or similar field
• Type: Full-time
• Salary: $115,000 - $145,000 USD

Millbrae

• 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
• Salary: $125,000 to $136,800

Oakland

• 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
• Salary: $335,000 - 375,000

South San Francisco

• Skills: regulatory affairs, INDs/CTAs, regulatory submissions, Health Authorities, clinical protocols, cross-functional teams, compliance, regulatory plans, global regulatory filings, CMC functions
• Experience: 7+ years or equivalent relevant experience in regulatory affairs in the biopharmaceutical industry

South San Francisco

• Skills: Medical Director, Rheumatology, Clinical Development, SLE program, TYK-2 inhibitor, Phase 2b study, Sponsor medical monitor, CRO collaboration, Data Monitoring Committee, Pharmacovigilance
• Experience: Licensed physician; Board certification in rheumatology or related field (desired); Industry experience in pharmacovigilance or clinical development (helpful).
• Salary: $285,000 - $325,000 USD annually

San Francisco

• 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
• Salary: $70,000

Redwood City

• Skills: Clinical Research, GCP, Regulatory Compliance, Data Verification, Site Monitoring, Clinical Trials, Recruitment Strategies, Document Maintenance, Audit Readiness, Collaboration
• Experience: Minimum of 4-6 years of experience in clinical research, including IVD experience.
• Type: Contract

Redwood City

• Skills: supply chain operations, logistics, inventory management, planning, data analytics, GMP, regulatory compliance, forecasting, cross-functional collaboration, clinical trials
• Experience: 5+ years of progressive experience in supply chain operations, with a focus on logistics, inventory management, and planning within biotech or pharmaceutical industry.
• Type: Contract
• Salary: $55 - $65 an hour

Palo Alto

• Skills: biostatistics, drug development, clinical study design, statistical analysis plans, exploratory analysis, FDA regulations, SAS programming, data analysis, cross-functional collaboration, clinical study reports
• Experience: PhD in statistics or equivalent, with at least 10 years of relevant experience in biotechnology or pharmaceutical industry
• Type: Full-time
• Salary: $225-240K/year

Palo Alto

• Skills: Medical Science Liaison, Neuroscience, Scientific relationships, Therapeutic areas, Research centers, Pipeline compounds, Clinical operations, Investigator initiated research, Cross-functional collaboration, Regulatory compliance
• Experience: Minimum of 3 years MSL experience or comparable role
• Type: Full-time

South San Francisco

• Skills: clinical trials, CRO management, regulatory standards, budget management, study protocols, GCP/ICH guidelines, team leadership, autoimmune disease, clinical budget, outsourcing
• Experience: At least 15 years in Clinical Operations, including 10+ years in management and 5+ years in autoimmune disease field
• Type: Full-time
• Salary: $235,000 - $280,000 USD per year

Hayward

• Skills: clinical trials, leadership, performance management, resource planning, employee development, operational excellence, mentorship, regulatory compliance, budget management, process improvements
• Type: other
• Salary: {'min': 165000.0, 'max': 185000.0, 'period': 'annual', 'currency': 'USD'}

Redwood City

• Skills: Clinical Research, Oncology, Monitoring, GCP/ICH Guidelines, Clinical Trials, Data Collection, Project Management, Medical Device, Study Protocol, Site Management
• Type: full_time
• Salary: {'min': 90400.0, 'max': 124300.0, 'period': 'annual', 'currency': 'USD'}

Berkeley

• Skills: Clinical Trial Manager, CRISPR, Clinical Operations, ICH-GCP, Vendor Management, Study Planning, Patient Enrollment, Data Management, Regulatory Compliance, CAR-T
• Type: full_time
• Salary: {'min': 150000.0, 'max': 165000.0, 'period': 'annual', 'currency': 'USD'}

Mountain View

• Skills: clinical studies, physiological research, data analysis, medical devices, statistical inferences, regulatory submissions, clinical data management, health and safety principles, clinical documentation, vendor management
• Type: full_time
• Salary: {'min': 117000.0, 'max': 160850.0, 'period': 'annual', 'currency': 'USD'}