Last updated: 2025-05-22

49 Clinical Operations Management jobs in San Francisco.

Hiring now: External Data Management @ Exelixis, Clinical Research Coordin @ Meta, Clinical Proj Mgr @ Neuralink, Associate Dir Clinical Op @ Arcus Bios, 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 .Explore more at at kaamvaam.com

🔥 Skills

clinical trials (17) project management (12) oncology (10) data management (10) clinical studies (9) compliance (8) clinical research (8) communication skills (8) regulatory compliance (7) GCP (6)

📍 Locations

South San Francisco (10) San Rafael (5) Alameda (4) Millbrae (4) Newark (4) Sunnyvale (4) Palo Alto (3) Redwood City (3) San Francisco (3) Burlingame (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…
Associate Clinical Data Management Director Alameda
Skills & Focus: data management, clinical trials, GCP, FDA regulations, data quality, EDC, process improvement, project management, compliance, vendor oversight
About the Company: Exelixis focuses on treating cancer and providing access to investigational therapies with a strong commitment to research and development.
Experience: A minimum of 9 years of related experience
Salary: $160,000 - $226,500
Type: Full-time
Benefits: comprehensive employee benefits package including 401k plan, medical, dental and vision coverage, life and disability i…
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…

Meta

Clinical Research Coordinator, Health and Wellbeing Burlingame
Skills & Focus: clinical research, health and wellbeing, human subjects, stakeholders, data collection, subject recruitment, study lifecycle, digital health, research execution, compliance management
About the Company: Meta builds technologies that help people connect, find communities, and grow businesses. When Facebook launched in 2004, it changed the way people connect. Ap…
Experience: 5+ years of experience with clinical research in either academic and/or commercial settings
Salary: $101,000/year to $152,000/year + bonus + equity + benefits
Type: Full Time
Benefits: Meta offers benefits including health, vacation, and more.
Clinical Study Operation Lead, Health and Wellbeing Burlingame
Skills & Focus: clinical research, operations, digital health, medical device, clinical study, protocol development, data management, remote clinical studies, multi-center, regulatory standards
About the Company: Meta builds technologies that help people connect, find communities, and grow businesses.
Experience: 8+ years in clinical research coordination/operations in industry and/or academic settings, or clinical setting in North America
Salary: $129,000/year to $185,000/year + bonus + equity + benefits
Type: Full Time
Benefits: Additional benefits include bonus, equity, and other benefits as listed in the posting.

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…

Arcus Biosciences

Associate Director, Clinical Operations Line Manager Hayward
Skills & Focus: clinical research, oncology, clinical operations, project management, team leadership, GCP, regulatory compliance, performance metrics, training and development, quality initiatives
About the Company: Arcus Biosciences is dedicated to developing innovative cancer immunotherapies with a focus on oncology research, aiming to improve patient outcomes.
Experience: 10+ years in clinical research, with 8+ years with an advanced degree; 4+ years as a direct line manager
Salary: $195,000 - $205,000 USD annually
Type: Full-time
Benefits: Stock programs, performance-based bonus, comprehensive benefits package
Sr. Manager, Site Budgets and Contracts (Contractor) Hayward
Skills & Focus: clinical trials, contracts, budgets, negotiation, oncology, compliance, FDA Regulations, GCPs, cross functional, risk management
Experience: 8+ years equivalent related business/industry experience, 5+ years experience with clinical budget negotiation
Type: Contract

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…
Clinical Trial Associate, Oncology Millbrae
Skills & Focus: clinical trials, oncology, study documents, data accuracy, trial master files, study initiation, investigator meetings, patient recruitment, regulatory compliance, team collaboration
About the Company: Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biolog…
Experience: Minimum of 3 days a week onsite presence; Bachelor's degree with 2 years of experience in a relevant field.
Salary: $104,000 to $114,000
Type: Full-time
Benefits: 401k plan with company matching, Medical, dental and vision insurance, Mental health and wellness benefits, Paid time o…
Senior Manager, Clinical Scientist Millbrae
Skills & Focus: clinical trial, clinical data, medical monitoring, protocol development, data analysis, regulatory requirements, oncology, clinical research, GCP, ICH
About the Company: Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enabl…
Experience: 10+ years with a Bachelor's degree, or 8+ years with a postgraduate degree
Salary: $163,000 to $178,600
Type: Full-time
Benefits: Bonus, equity, 401k, medical, dental, vision, mental health, wellness benefits, paid time off, life insurance, parental…

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…
Lead Study Biostatistician Palo Alto
Skills & Focus: biostatistics, drug development, clinical study design, statistical analysis plans, exploratory analysis, FDA regulations, SAS programming, data analysis, cross-functional collaboration, clinical study reports
About the Company: Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. They are advancing progra…
Experience: PhD in statistics or equivalent, with at least 10 years of relevant experience in biotechnology or pharmaceutical industry
Salary: $225-240K/year
Type: Full-time
Benefits: 401(k) plan with company match, Medical, dental, and vision plans, Company-offered Life and AD&D insurance, Company-pro…

Adverum Biotechnologies, Inc.

Preclinical Study Monitor Redwood City
Skills & Focus: CRO Management, Study Oversight, GLP compliance, Data Management, Regulatory requirements, Communication, Collaboration, Drug development, Protocol development, Record-keeping
About the Company: Adverum Biotechnologies is a clinical-stage gene therapy company targeting unmet medical needs in ophthalmology and rare diseases. Adverum develops gene therap…
Experience: Minimum 5 years of relevant experience in preclinical study monitoring.
Salary: $124,092 - $133,013
Type: Full-time
Benefits: Employees in this position are eligible to participate in the applicable Company equity incentive award plan. The compa…

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…
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…

Clearview Healthcare Partners

Primary Research Coordinator San Francisco
Skills & Focus: market research, healthcare, biological sciences, expert network, project management, scheduling, communication, consulting, expertise, compliance
About the Company: ClearView Healthcare Partners is a premier life sciences strategy consulting firm headquartered in Boston, with offices in San Francisco, New York City, London…
Experience: Minimum of 1-2 years' work experience in a healthcare-related field or life sciences firm.
Salary: $70,000
Type: Full-time
Benefits: Annual discretionary performance bonus and a comprehensive benefits package.

Precision Medicine Group

Clinical Trial Manager San Francisco
Skills & Focus: clinical trial management, project timeline adherence, quality delivery, clinical research, monitoring, regulatory documentation, data cleaning, collaborative environment, communication skills, clinical trial activities
About the Company: We are a team of clinical trial experts who are dedicated to the success of our clients so that patients can receive much-needed treatments. We have nurtured a…
Experience: 5-7 years of clinical research experience with significant clinical monitoring experience.
Type: Full-time

Iqvia

Data Team Lead San Francisco
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.

Biomarin Pharmaceutical Inc.

Associate Director Global Study Operations San Rafael
Skills & Focus: clinical trial management, people management, leadership, coaching, process improvement, stakeholder engagement, compliance, project scope, communication, team development
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: Minimum of 8 years in the pharmaceutical industry with a BA/BS degree with a focus on life sciences, nursing, or related technical or scientific discipline or 6 years in the pharmaceutical industry with a master’s degree.
Vendor Laboratory Manager (VLM) San Rafael
Skills & Focus: vendor oversight, clinical studies, biospecimen management, project management, biomarker operations, quality standards, clinical protocol, risk mitigation, stakeholder communication, clinical operations
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: 3+ years project management, and/or clinical operations experience.

Biomarin

Medical Writer (TEMPORARY) San Rafael
Skills & Focus: Medical Writing, Clinical Studies, Submissions, Document Preparation, Protocols, Informed Consent Forms, Safety Reports, Regulatory Submissions, Documentation Management, Biotechnology
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: At least 5 years experience required
Salary: null to null per hour
Type: Contract
Benefits: Includes a discretionary bonus and/or long-term incentive units, and full range of medical, financial, and/or other ben…

Biomarin Pharmaceutical Inc.

Associate Director, Clinical Medical Writing San Rafael
Skills & Focus: Medical Writing, Regulatory submissions, Clinical studies, Document development, Team management, Cross-functional collaboration, Budgeting, Clinical development, Vendor management, Project management
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: At least 10 years of experience as a medical writer in the pharmaceutical industry. Minimum of 3 years administrative and/or functional management experience as a manager of a medical writer team or department in a clinical development setting.
Associate Director Global Study Operations San Rafael
Skills & Focus: clinical trials, management experience, drug development, team leadership, process improvement, communication skills, cross-functional collaboration, vendor oversight, training programs, regulatory compliance
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: Minimum of 8 years in the pharmaceutical industry with a BA/BS degree or 6 years with a master's degree.
Type: Full-time

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…
Senior Director, Clinical Operations South San Francisco
Skills & Focus: clinical trials, CRO management, regulatory standards, budget management, study protocols, GCP/ICH guidelines, team leadership, autoimmune disease, clinical budget, outsourcing
About the Company: Alumis Inc. is a precision medicines company dedicated to transforming the lives of patients with autoimmune diseases.
Experience: At least 15 years in Clinical Operations, including 10+ years in management and 5+ years in autoimmune disease field
Salary: $235,000 - $280,000 USD per year
Type: Full-time
Benefits: Health insurance, stock options, annual bonus, free onsite gym, generous PTO, cell phone stipend, Genentech bus & ferry…
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…

Bridgebio Oncology Therapeutics

Clinical Scientist - Oncology South San Francisco
Skills & Focus: clinical development, oncology, clinical studies, protocol writing, data analysis, collaboration, medical monitoring, clinical trials, team environment, strategic planning
About the Company: BridgeBio Oncology Therapeutics (“BBOT”) is a clinical-stage company focused on developing novel therapeutics to address unmet needs in RAS-driven tumors.
Experience: At least 3 years of oncology clinical development experience
Salary: $193,000 - $222,000 USD
Type: Full-time
Benefits: Market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous…

Ideaya Biosciences

Study Lead South San Francisco
Skills & Focus: Study Lead, clinical trials, clinical activities, cross-functional, clinical programs, trial planning, execution, Medial Monitor, Biostatistics, Translational Science
About the Company: IDEAYA Biosciences is a public, clinical-stage precision medicine oncology company committed to the discovery, development, and commercialization of targeted t…

Maze Therapeutics

Associate Director of Clinical Operations South San Francisco
Skills & Focus: Clinical trial execution, Leadership, Vendor management, Budget oversight, Data quality, Regulatory compliance, Process optimization, Clinical operations, Cross-functional collaboration, Strategic thinking
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: 8–10 years of clinical operations experience, including leadership of Phases I–III trials
Salary: $194,000 - $237,000
Type: Full-time
Benefits: competitive medical, dental, and vision insurance, mental health offerings, equity incentive plan, 401(k) program with …
Associate Director of Clinical Operations South San Francisco
Skills & Focus: Clinical trial execution, Leadership, Vendor management, Budget oversight, Data quality, Regulatory compliance, Process optimization, Clinical operations, Cross-functional collaboration, Strategic thinking
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: 8–10 years of clinical operations experience, including leadership of Phases I–III trials
Salary: $194,000 - $237,000
Type: Full-time
Benefits: competitive medical, dental, and vision insurance, mental health offerings, equity incentive plan, 401(k) program with …
Associate Director of Clinical Operations South San Francisco
Skills & Focus: Clinical trial execution, Leadership, Vendor management, Budget oversight, Data quality, Regulatory compliance, Process optimization, Clinical operations, Cross-functional collaboration, Strategic thinking
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: 8–10 years of clinical operations experience, including leadership of Phases I–III trials
Salary: $194,000 - $237,000
Type: Full-time
Benefits: competitive medical, dental, and vision insurance, mental health offerings, equity incentive plan, 401(k) program with …

Abbvie

Clinical Scientist II South San Francisco
Skills & Focus: clinical trials, drug development, scientific data, program strategy, study protocols, Good Clinical Practices, pharmacovigilance standards, research collaborations, clinical study report, regulatory documents
About the Company: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tom…
Experience: Bachelors/Masters with 13+ years of experience, advanced Degree 3+ years of experience
Salary: $121,000 - $230,000
Type: Full-time
Benefits: A comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance…

Intuitive Surgical

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.
Senior Clinical Study Manager Sunnyvale
Skills & Focus: clinical studies, evidence generation, clinical protocols, project management, regulatory compliance, biostatistics, clinical research, data analysis, stakeholder engagement, medical device trials
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: 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
Clinical Study Manager III Sunnyvale
Skills & Focus: clinical studies, evidence generation, regulatory approvals, clinical protocols, research studies, data management, monitoring, clinical research, protocol development, medical device trials
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…