52 Clinical Operations Management jobs in San Jose.

Hiring now: External Data Management @ Exelixis, Clinical Proj Mgr @ Neuralink, Clinical Trial Mgr @ Grail, Dir Clinical Ops Study Ma @ Eikon Ther, Clinical Trial Management @ Ardelyx, Data Team Lead @ Iqvia, Sr Dir Clinical Developme @ Aditum Bio, Clinical Research Associa @ Bridgebio , Associate Dir Global Phar @ Ascendis P, Proj Mgr Cmc @ Adverum Bi.Explore more at jobswithgpt.com.

🔥 Skills

clinical trials (14) project management (14) data management (11) clinical trial (10) oncology (9) vendor management (9) clinical research (8) clinical operations (7) clinical studies (7) regulatory requirements (6)

đź“Ť Locations

South San Francisco (10) Redwood City (7) San Jose (6) Sunnyvale (5) Alameda (4) Millbrae (4) Newark (4) Santa Clara (4) Fremont (2) Oakland (2)
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Exelixis

External Data Management Director Alameda
Skills & Focus: 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
Salary: $181,500 - $257,500 annually
Type: Full-time
Benefits: 401k with company contributions, group medical, dental, vision coverage, life insurance, flexible spending accounts, an…
Senior Drug Safety Operations Manager Alameda
Skills & Focus: drug safety, clinical trials, case processing, vendor management, pharmacovigilance, SOP development, MedDRA coding, collaboration, safety management, analysis
Experience: 9 years of related experience with a BS/BA degree, or 7 years with MS/MA degree, or 2 years with PhD
Salary: $149,500 - $213,000 annually
Type: Full-time
Benefits: Comprehensive employee benefits package including 401k, medical, dental, and vision coverage, life and disability insur…
Associate Clinical Supply Chain Director Alameda
Skills & Focus: clinical supplies strategy, clinical trial management, packaging and labeling, inventory management, drug supply, interactive response technology, clinical operations, vendor collaboration, regulatory affairs, project management
About the Company: A biotechnology company focused on innovative R&D, including discovery, clinical trials, and collaborations aimed at treating cancer.
Experience: Minimum of eleven years related experience for BS/BA or nine years for MS/MA in related discipline.
Salary: $152,000 - $215,000 annually
Type: Full-time
Benefits: Comprehensive benefits package including a 401k plan, medical, dental, vision coverage, life and disability insurance, …

Neuralink

Clinical Project Manager Fremont
Skills & Focus: clinical trials, clinical studies, Good Clinical Practice, compliance, medical devices, ISO14155, communication, project management, neuroscience, regulatory requirements
About the Company: We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to th…
Experience: 5+ years of academic or industry experience working with medical devices
Salary: $105,000 - $195,000 USD
Type: Full-time
Benefits: Full-time employees are eligible for excellent medical, dental, and vision insurance through a PPO plan, paid holidays,…
Clinical Research Associate Fremont
Skills & Focus: clinical trials, Clinical Research Associate, GCP, FDA, ICH guidelines, monitoring, regulatory compliance, patient recruitment, medical device studies, data capture systems
About the Company: We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to th…
Experience: Minimum of 5 years of experience working in clinical trials with 3 years as a Clinical Research Associate
Salary: $89,000 — $148,000 USD
Type: Full-time
Benefits: An opportunity to change the world and work with some of the smartest and most talented experts; Growth potential; Exce…

Grail

Clinical Trial Manager Menlo Park
Skills & Focus: clinical trial, clinical operations, relationship management, site management, cross functional teams, problem solving, compliance, efficiency, fast paced environment, ambiguity
About the Company: We are a healthcare company, pioneering new technologies to advance early cancer detection. We have built a multi-disciplinary organization of scientists, engi…

Eikon Therapeutics

Director, Clinical Operations Study Management Millbrae
Skills & Focus: clinical operations, study management, global clinical trials, regulatory compliance, oncology, team leadership, protocols, Good Clinical Practice (GCP), management expertise, budget management
About the Company: Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biolog…
Experience: 12+ years with a Bachelor's degree or 10+ years with a post graduate degree
Salary: $226,000 to $247,000
Type: Full-time
Benefits: 401k plan with company matching, Medical, dental and vision insurance, Mental health and wellness benefits, Generous pa…
Senior Clinical Trial Manager, Oncology Millbrae
Skills & Focus: Clinical Trials, Oncology, Project Management, Leadership, Regulatory Compliance, Patient Recruitment, Data Management, Quality Assurance, Budget Management, Cross-functional Collaboration
About the Company: Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biolog…
Experience: 6+ years with a Post Graduate degree or 8+ years with a Bachelor's degree in a relevant field.
Salary: $143,000 to $156,750
Type: Full-time
Benefits: 401k plan with company matching, medical, dental and vision insurance, mental health and wellness benefits, generous pa…
Clinical Trial Manager, Oncology Millbrae
Skills & Focus: clinical trial management, oncology, regulatory compliance, project management, data management, clinical operations, patient care, ICH-GCP, FDA guidelines, communication skills
About the Company: Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biolog…
Experience: 3 to 8 years depending on education level
Salary: $130,000 to $142,500
Type: Full-time
Benefits: 401k plan with company matching, 95% medical premiums covered, dental and vision premiums covered, mental health benefi…

Ardelyx

Clinical Trial Management Associate Newark
Skills & Focus: clinical trial, CRO, vendor management, regulatory submissions, medical terminology, clinical development, study documentation, communication skills, proficiency in MS Office, study materials
About the Company: Ardelyx is a publicly traded commercial biopharmaceutical company founded with a mission to discover, develop and commercialize innovative first-in-class medic…
Experience: 3+ years of experience in clinical trial operations
Salary: $93,000 - $113,000
Type: Full-time
Benefits: Ardelyx offers a robust benefits package including a 401(k) plan with employer match, paid parental leave, health plans…
Clinical Trial Associate Newark
Skills & Focus: Clinical Trial Management, data verification, regulatory guidance, clinical trials, protocol deviations, adverse events, Microsoft applications, clinical protocols, ICH/GCP regulations, teamwork
About the Company: Ardelyx is a publicly traded commercial biopharmaceutical company founded with a mission to discover, develop and commercialize innovative first-in-class medic…
Experience: 2+ years of experience in Clinical operations or healthcare-related experience
Salary: $85,000-$103,000
Type: Full-time
Benefits: 401(k) plan with generous employer match, 12 weeks of paid parental leave, up to 12 weeks of living organ and bone marr…
Clinical Trial Management Associate Newark
Skills & Focus: clinical trial, CRO, medical terminology, ICH GCP Guidelines, regulatory submissions, study documentation, clinical studies, progress reports, MS Office, communication skills
About the Company: Ardelyx is a publicly traded commercial biopharmaceutical company founded with a mission to discover, develop and commercialize innovative first-in-class medic…
Experience: 3+ years of experience in clinical trial operations
Salary: $93,000 - $113,000
Type: Full-time
Benefits: 401(k) plan with generous employer match, 12 weeks of paid parental leave, flexible time off, health plans (medical, pr…

Iqvia

Data Team Lead Oakland
Skills & Focus: data management, clinical data management, project management, negotiations, quality management, financial tracking, process improvements, Good Clinical Practices, regulatory guidelines, compliance
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 5 years direct Data Management experience, including 3 or more years as a CDM project lead.
Salary: $82,300.00 - $173,900.00
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Aditum Bio

Senior Director, Clinical Development Oakland
Skills & Focus: Clinical Trial Design, Clinical Trials, Phase I, Phase II, Medical Monitoring, Safety Oversight, Regulatory Requirements, Compliance, Clinical Strategy, Cross-functional Team
About the Company: At Aditum Bio our mission is to provide access to medicines to patients in need. Co-founded by industry veterans Joe Jimenez, former CEO of Novartis and Mark F…
Experience: A minimum of 6 years of industry experience in clinical development in a pharmaceutical or biotech company setting.
Salary: $335,000 - 375,000
Type: Full-time
Benefits: medical, dental, vision, and 401k

Bridgebio Pharma

Clinical Research Associate Palo Alto
Skills & Focus: clinical studies, Good Clinical Practice (GCP), Trial Master File (TMF), monitoring, site management, regulatory submissions, data entry, quality reviews, clinical trial documentation, problem-solving
About the Company: BridgeBio is a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic dise…
Experience: Minimum 4-6 years of experience within clinical operations, study coordinator, or similar field
Salary: $115,000 - $145,000 USD
Type: Full-time
Benefits: Market-competitive total rewards package including base pay, performance bonus, company equity, and generous health ben…

Ascendis Pharma

Associate Director, Global Pharmacovigilance Operations Palo Alto
Skills & Focus: 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)
About the Company: Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. We are advancing programs…
Experience: Minimum of 8 years recent experience in Pharmacovigilance required; relevant pharmaceutical industry experience in drug safety required.
Benefits: 401(k) plan with company match; Medical, dental, and vision plans; Company-offered Life and Accidental Death & Dismembe…

Adverum Biotechnologies, Inc.

Project Manager, CMC Redwood City
Skills & Focus: CMC, Project Management, Pharma, Process Development, Quality Control, Quality Assurance, Meeting Facilitation, Timeline Management, GMP Manufacturing, Clinical
About the Company: Adverum Biotechnologies, Inc. is a mission-driven clinical-stage company that aims to establish gene therapy as a new standard of care for highly prevalent ocu…
Experience: 1-2 years of project management experience in the Pharma CMC space
Salary: $73,500 - $82,536 a year
Type: Full Time
Benefits: Employees in this position are eligible to participate in the applicable Company equity incentive award plan. The amoun…
Senior Medical Monitor (Senior Director) Redwood City
Skills & Focus: medical monitoring, clinical trials, pharmacovigilance, drug safety, safety data, clinical protocols, adverse events, ICH/GCP guidelines, clinical research, safety documentation
About the Company: Adverum Biotechnologies, Inc. is a mission-driven clinical-stage company that aims to establish gene therapy as a new standard of care for highly prevalent ocu…
Experience: 10-12 years direct experience in medical monitoring and/or pharmacovigilance and/or drug safety experience
Salary: $305,000 - $327,000
Type: Full Time
Benefits: Employees are eligible to participate in the company’s standard employee benefit programs including medical, dental, vi…

Arcellx

Lead Data Manager Redwood City
Skills & Focus: data management, clinical studies, database activities, protocol review, data integrity, data cleaning, oncology, Medidata RAVE, regulatory guidelines, communication skills
About the Company: Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other…
Experience: Minimum of 7 years of clinical data management experience in the pharmaceutical, biotechnology industry or in a CRO.
Salary: $180,000 - $195,000 per year
Type: Full-time
Benefits: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every…
Clinical Operations Leader Redwood City
Skills & Focus: clinical trials, oncology, project management, clinical operations, trials initiation, quality checks, regulatory requirements, team-oriented, data quality, SOPs
About the Company: Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other…
Experience: 8+ years of clinical operations experience with both early and late-stage oncology clinical trials; 2+ years of direct line management experience.
Salary: $190k - $205,000 per year
Type: Full-time
Benefits: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every…

Biomea Fusion

Clinical Pharmacologist DMPK Redwood City
Skills & Focus: clinical pharmacology, DMPK, pharmacokinetics, data analysis, modeling, clinical study protocols, regulatory documents, multi-disciplinary team, population PK, in vitro ADME
About the Company: At Biomea Fusion, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients.
Experience: At least 2-3 years of relevant industry experience
Salary: $125,000 to $145,000
Type: Full-Time
Benefits: Competitive benefits package, opportunity to participate in stock programs, performance-based bonus programs

Adverum Biotechnologies, Inc.

Director/Senior, Clinical Program Management Redwood City
Skills & Focus: clinical trial management, program management, cross-functional teams, strategic planning, Phase 3 studies, clinical operations, data management, regulatory compliance, clinical program strategy, project management tools
About the Company: Adverum Biotechnologies, Inc. is a mission-driven clinical-stage company that aims to establish gene therapy as a new standard of care for highly prevalent ocu…
Experience: Minimum of 10-12+ years of experience in clinical program management or clinical trial operations within the biotech, pharmaceutical, or CRO industry.
Salary: $216,000 - $250,000
Type: Full Time
Benefits: Employees are eligible to participate in the Company’s standard employee benefit programs, which currently include medi…

Arcellx

Manager, Clinical Quality Redwood City
Skills & Focus: Clinical Quality, GCP, audit plans, regulatory standards, clinical trials, biotechnology, risk assessment, communication skills, compliance guidance, training development
About the Company: Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other…
Experience: 8+ years’ experience working within GCP in a pharmaceutical or biologics environment.
Salary: $135,000 - $155,000
Type: Full-time
Benefits: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every…

Iqvia

Sr. CRA, Sponsor Aligned, Oncology San Jose
Skills & Focus: Clinical Research Associate, monitoring, clinical trial, oncology, GCP, ICH guidelines, site visits, patient recruitment, quality assurance, documentation
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 3+ years of on site oncology monitoring experience strongly preferred. 1.5+ years of oncology monitoring experience can be considered.
Salary: $71,900.00 - $189,000.00
Type: Full-time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
Clinical Research Associate, Sponsor Dedicated San Jose
Skills & Focus: monitoring, site management, clinical research, Good Clinical Practice, protocol, data integrity, regulatory requirements, subject recruitment, documentation, communication
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: At least 2 years of on-site monitoring experience.
Salary: $71,900.00 - $189,000.00
Type: Full time
Benefits: Benefits programs designed to meet total well-being needs.

Parexel

Contract & Proposal Manager San Jose
Skills & Focus: Administrative, Clinical Research, Project Leadership, Biostatistics, Regulatory, Consulting, Clinical Trials, Clinical Operations, Diversity & Inclusion, Hiring Process
About the Company: Parexel is a global biopharmaceutical services organization that provides a range of services to improve the health of patients and patients' access to medicat…
Type: Contract
Benefits: Flexible Work Arrangement, Work-life balance, Corporate Responsibility approach

Iqvia

CRA 2 - Oncology San Jose
Skills & Focus: clinical research, site monitoring, oncology, GCP, ICH, protocol adherence, regulatory requirements, project management, data integrity, communication
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: At least 1.5 years of on-site monitoring experience.
Salary: $87,200.00 - $189,000.00
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Kyowa Kirin North America

Director, Clinical Operations- Clinical Trial Execution San Jose
Skills & Focus: clinical operations, clinical trials, project planning, resource management, regulatory guidelines, clinical management, stakeholder management, clinical development, cross functional, CRO selection
About the Company: Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in …
Experience: Minimum 12 years of experience in study management at a sponsor/biotechnology/pharmaceutical company. Minimum 5 years demonstrated managerial, organizational, and leadership skills in a dynamic environment running multiple clinical trials.

Parexel

Clinical Research Associate (CRA) San Jose
Skills & Focus: Clinical Research, Associate, CRA, Clinical Trials, Pharmaceutical, Biotechnology, Monitoring, Regulatory, Site Care, Data Management
About the Company: Parexel is a global consulting firm specializing in providing comprehensive drug development services to the pharmaceutical and biotechnology industries.

Johnson & Johnson

Principal Clinical Research Associate – Shockwave Medical Santa Clara
Skills & Focus: clinical research, project management, clinical trial, vendors, regulatory standards, protocol compliance, data collection, investigational sites, study design, clinical data
About the Company: Johnson & Johnson is a global leader in healthcare innovation, aiming to prevent, treat, and cure complex diseases through smarter and less invasive treatments.
Experience: Minimum 10 years’ experience directly supporting clinical research
Type: Full-time
Assoc. Director Clinical and Preclinical Santa Clara
Skills & Focus: clinical research, preclinical research, evidence generation, regulatory submissions, project management, team leadership, medical devices, biologics, global clinical trials, strategic assessment
About the Company: Johnson & Johnson is a global leader in healthcare innovation, empowering breakthroughs in preventing, treating, and curing complex diseases.
Experience: Minimum of 8 years of related scientific/technical experience, including leadership/management; minimum of 2 years of people management-related experience.
Salary: $168,000 to $271,000
Type: Full-time
Benefits: Annual performance bonus based on individual and corporate performance; competitive, performance-based compensation pro…
Associate Project Head - OTTAVA Capital Santa Clara
Skills & Focus: project management, medical devices, capital equipment, cross-functional team leadership, regulatory requirements, clinical affairs, risk management, strategic planning, agile framework, collaboration
About the Company: Johnson & Johnson's Family of Companies is focused on healthcare innovation to improve patient outcomes and advance medical technology.
Experience: 8+ years of relevant industry experience, including 3+ years of people management
Type: Fully Onsite

Alumis Inc.

Director, Biostatistics South San Francisco
Skills & Focus: Biostatistics, clinical trials, statistical analysis plans, CRO management, regulatory submissions, data quality, simulation work, integrated analyses, clinical study design, statistical deliverables
About the Company: Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases.
Experience: Ph.D. in Biostatistics with at least 8 years of experience, or Master’s with a minimum of 10 years of directly relevant experience.
Salary: $245,000 - $255,000
Type: Full-time
Benefits: Generous stock option grants, annual bonus program, health insurance premiums paid at 90% for employees, 80% for depend…

Ideaya Biosciences

Director of DMPK-Clinical Pharmacology South San Francisco
Skills & Focus: DMPK, Clinical Pharmacology, project progression, cross-functional teams, strategic leadership, development strategy, registration requirements, early-stage programs, late-stage programs, oncology
About the Company: IDEAYA Biosciences (NASDAQ: IDYA) is a public, clinical-stage precision medicine oncology company committed to the discovery, development, and commercializatio…
Experience: significant clinical pharmacology experience

Biogen

Clinical Trial Manager South San Francisco
Skills & Focus: Clinical Trial Management, Operational Strategy, Clinical Research Organization, Protocol Development, Study Delivery, Site Feasibility, Risk Mitigation, Budget Management, Team Operations, Regulatory Compliance
About the Company: Biogen’s West Coast Hub, based in South San Francisco, is specifically focused on transforming the lives of patients with severe immune-mediated diseases by de…
Type: Hybrid

Alumis Inc.

Medical Director, Rheumatology South San Francisco
Skills & Focus: Medical Director, Rheumatology, Clinical Development, SLE program, TYK-2 inhibitor, Phase 2b study, Sponsor medical monitor, CRO collaboration, Data Monitoring Committee, Pharmacovigilance
About the Company: Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases.
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
Benefits: Health insurance premiums paid at 90% for employee, 80% for dependents; Free access to Genentech Bus & Ferry Share prog…

Maze Therapeutics

Senior Clinical Trial Specialist South San Francisco
Skills & Focus: Clinical Operations, clinical trial, vendor management, ICH/GCP Guidelines, study protocols, documentation, process improvement, data management, sample analysis, SOP development
About the Company: Maze Therapeutics is a clinical-stage biopharmaceutical company harnessing the power of human genetics to develop novel, small molecule precision medicines for…
Experience: 2-3+ years in Clinical Operations within a biotech or pharmaceutical environment
Salary: $126,000 to $154,000
Type: Full-time
Benefits: competitive medical, dental, and vision insurance, mental health offerings, equity incentive plan, 401(k) program with …
Senior Clinical Trial Specialist South San Francisco
Skills & Focus: Clinical Operations, clinical trial, vendor management, ICH/GCP Guidelines, study protocols, documentation, process improvement, data management, sample analysis, SOP development
About the Company: Maze Therapeutics is a clinical-stage biopharmaceutical company harnessing the power of human genetics to develop novel, small molecule precision medicines for…
Experience: 2-3+ years in Clinical Operations within a biotech or pharmaceutical environment
Salary: $126,000 to $154,000
Type: Full-time
Benefits: competitive medical, dental, and vision insurance, mental health offerings, equity incentive plan, 401(k) program with …
Senior Clinical Trial Specialist South San Francisco
Skills & Focus: Clinical Operations, clinical trial, vendor management, ICH/GCP Guidelines, study protocols, documentation, process improvement, data management, sample analysis, SOP development
About the Company: Maze Therapeutics is a clinical-stage biopharmaceutical company harnessing the power of human genetics to develop novel, small molecule precision medicines for…
Experience: 2-3+ years in Clinical Operations within a biotech or pharmaceutical environment
Salary: $126,000 to $154,000
Type: Full-time
Benefits: competitive medical, dental, and vision insurance, mental health offerings, equity incentive plan, 401(k) program with …

Alumis Inc.

Associate Director, Data Management South San Francisco
Skills & Focus: clinical trial data, data management, Case Report Form, clinical database, Data Management Plans, data quality, vendor management, eCRF specifications, data integration, clinical research regulations
About the Company: Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases.
Experience: 10+ years of relevant experience
Salary: $195,000 USD to $220,000 USD annually
Type: Full-time
Benefits: Health insurance premiums paid at 90% for employee, 80% for dependents. Free access to Genentech Bus & Ferry Share prog…

Biogen

Clinical Trial Manager South San Francisco
Skills & Focus: clinical trial, CRO, operational strategy, protocol development, budget management, site feasibility, risk mitigation, compliance, scientific meetings, team operations
About the Company: Biogen’s West Coast Hub is focused on transforming the lives of patients with severe immune-mediated diseases by developing novel targeted therapies.

Intuitive Surgical

Sr. Manager, Clinical Affairs – Emerging Technology Sunnyvale
Skills & Focus: clinical trials, clinical protocols, regulatory submissions, clinical study strategy, cross-functional collaboration, budget management, investigational sites, data management, project management, communication skills
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: 12+ years of professional experience with at least 3-5 years of supervisory experience preferred; Minimum of 5 years of experience managing clinical studies autonomously through different study phases.
Type: Full-time
Senior Clinical Study Manager Sunnyvale
Skills & Focus: clinical studies, clinical research, regulatory approvals, protocol development, site selection, compliance, data management, biostatistics, clinical trial agreements, monitoring
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: 5-10 years of experience in clinical research
Type: Full-time

Ceribell, Inc

Director, Clinical Operations Sunnyvale
Skills & Focus: Clinical Operations, Protocol Development, Site Qualification, IRB Process Navigation, Patient Enrollment, Data Monitoring, Compliance, Quality Assurance, Strategic Contribution, Regulatory Requirements
About the Company: Ceribell is a medical technology company focused on transforming the diagnosis and management of patients with serious neurological conditions. The Ceribell Sy…
Experience: Minimum of 8-10 years of experience in clinical operations within the medical device industry.
Salary: $220,000 - $235,000 USD
Type: Hybrid
Benefits: Annual Bonus Opportunity + Ceribell Equity, 100% Employer paid Health Benefits for the Employee, Life & Long-term disab…

Intuitive Surgical

Sr. Clinical Research Associate Sunnyvale
Skills & Focus: Clinical Research, Medical Devices, Good Clinical Practice, Clinical Trials, Regulatory Compliance, Data Management, Clinical Monitoring, Patient Recruitment, Study Design, Protocol Development
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: Typically requires a minimum of 8 years of related experience.
Type: Full-time
Benefits: Market-competitive compensation packages, inclusive of base pay, incentives, benefits, and equity.
Senior Clinical Study Manager Sunnyvale
Skills & Focus: clinical studies, regulatory approvals, clinical trial strategy, clinical protocols, study design, monitoring, protocol compliance, study documents, patient recruitment, literature review
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: 5 years in clinical research with advanced degree, or 8 years with bachelor's, or 10 years of relevant experience.

Sgs

Jr. Clinical Research Coordinator Union City
Skills & Focus: clinical studies, protocol, Good Clinical Practices, Standard Operating Procedures, study documentation, Electronic Data Capture, recruiting materials, scheduling subjects, quality assurance, customer service