49 trial manager jobs at 20 companies in Watsonville, CA
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Clinical Trial Manager
San Carlos, California, United States
$129k-$218k/yrHybridFull Time
IntuitiveNASDAQ: ISRG: Robotic-assisted systems for minimally invasive surgery.
3+ YOERequires 3+ years of clinical trial operations experience in medical devices or diagnostics, multi-site study and CRO/vendor coordination, GCP/ICH knowledge, project management skills, and a relevant bachelor's degree.
Imperative Care: Develops medical devices for stroke and vascular disease treatment.
5+ YOE1+ Mgmt5+ years of clinical research management, preferably in medical devices; IDE studies; FDA/GCP knowledge; strong collaboration and communication; willingness to travel 20-30%
Clinical Data Management Systems, Regulatory Compliance, GCP, FDA Regulations, IDE
Akura Medical: Developing catheter-based mechanical thrombectomy platforms for VTE treatment.
7+ YOE7+ years managing medical device clinical trials including start-up, monitoring oversight, and closeout; strong knowledge of ICH GCP, ISO 14155, and FDA regulations; experience with CROs, EDC, budgeting, and regulatory inspections.
Ascendis PharmaNASDAQ: ASND: Develops long-acting prodrug therapies for rare diseases and oncology.
7+ YOEBachelor’s or master’s degree in natural or health sciences preferred, 7+ years managing or monitoring Phase 1–3 trials, ICH-GCP expertise, vendor management, site monitoring, and proficiency with Veeva Systems, CTMS, Endpoint IRT, and Microsoft Office.
Veeva Systems, Clinical Vault eTMF, Veeva EDC, CTMS, Endpoint IRT, Microsoft Office, Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint
KemperNYSE: KMPR: Provides specialized auto, life, and health insurance services.
3+ YOE3+ years trial attorney experience, membership in the State Bar, insurance-defense experience preferred, ability to travel as needed, use case management software, and produce timely status reports.
Stanford University: A private research university providing higher education and research.
2+ YOEBachelor's degree and 2 years clinical research experience; knowledge of clinical trials data management, regulatory requirements (HIPAA,FDA,IRB,GCP), medical terminology, Microsoft Office; supervisory experience.
Business Development Senior Specialist – Litigation & Trial
San Francisco or Redwood City or New York City or Washington or Chicago
$100k-$125k/yrHybridFull Time
Latham & Watkins: Global law firm providing legal services for complex corporate matters.
4+ YOEBachelor's degree, minimum 4 years related experience (2 years in litigation practice), strong research, analysis, and business development skills; ability to manage multiple priorities.
2+ YOELead statistical execution for clinical programs, manage external statisticians/programmers, evaluate CDISC packages, proficiency in SAS and R, MS/PhD preferred, and minimum 2 years clinical trial experience.
Elite Clinical Network: Clinical research network operating sites for pharmaceutical trials.
1+ YOE1–2 years clinical research experience, basic understanding of trial operations and regulations, strong communication and organizational skills, familiarity with Microsoft Office and clinical trial systems, bachelor's degree preferred.
VaxcyteNASDAQ: PCVX: Developing vaccines to prevent and treat bacterial diseases.
9+ YOEBachelor's in life sciences/supply chain,9+ years clinical supply management,experience with blinded clinical supplies,vaccine trials,Veeva,GMP,cold-chain packaging,global regulatory labeling,and cross-functional leadership.
Stanford University: Private research university providing academic education and medical services.
2+ YOEBachelor's degree and 2 years clinical research experience (or equivalent); knowledge of clinical trials data management, HIPAA/FDA/IRB/GCP, Microsoft Office and database applications; strong interpersonal and communication skills; thoracic clinical knowledge preferred.
Summit TherapeuticsNASDAQ: SMMT: Developing oncology therapies to improve patient quality of life.
10+ YOE10+ years clinical data management experience in biotech/pharma, EDC and data standards experience, MedDRA/WHODRUG knowledge, leadership and CRO/vendor oversight, understanding of FDA/ICH/GCP and clinical trial data processes.
Attovia Therapeutics: Creates biotherapeutics for treating immune-mediated diseases and oncology.
1+ YOEBachelor's degree in life sciences, nursing, health sciences, or related field; 1–3 years supporting clinical trials; ICH-GCP knowledge; strong organization, communication, detail management, and Microsoft Office proficiency.
Microsoft Office, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, Veeva Vault TMF, Wingspan, CTMS, eISF, EDC, electronic quality management systems
Law Foundation of Silicon Valley: Provides free legal services and advocacy for underrepresented people
10+ YOEJ.D. and active California Bar, 10+ years legal experience, proven impact litigation and trial record, significant management/mentorship experience, ability to secure attorneys' fees, and strategic communications experience.
Product Marketing Specialist - Product Led Growth (PLG)
Sunnyvale, California, United States
$109k-$125k/yrOnsiteFull Time
Illumio: Provides zero-trust segmentation software to contain cyberattacks.
2+ YOE2+ years product marketing experience in enterprise security or cloud infrastructure, strong written/verbal communication, project management, technical aptitude, and experience defining PLG web trial and marketplace journeys.
AbbottNYSE: ABT: Manufactures medical devices, diagnostics, and nutritional health products.
8+ YOEBachelor's degree and minimum 8 years conducting clinical studies; experience with medical device trials, IDE/TAVR preferred; knowledge of device regulations; experience with safety, physician management, and external research committees.
York Law Firm: Personal injury and elder abuse law firm in Sacramento.
5+ YOEMinimum 5 years litigation paralegal experience (California preferred). Strong federal and CA court rules knowledge, discovery and trial support experience, legal drafting, e-discovery, case management, and advanced Microsoft Office skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
Protagonist TherapeuticsNASDAQ: PTGX: Developing oral peptide therapeutics for complex diseases.
10+ YOEAdvanced degree in pharmaceutical, pharmacology-related, or quantitative sciences; 10+ years of industry experience; clinical pharmacology, PK/PD, modeling, clinical trials, regulatory, and cross-functional leadership experience.