Clinical trials management jobs in California (CA) State

If you are a Jazz employee please apply via the Internal Career site Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people ...

If you are a Jazz employee please apply via the Internal Career site Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people ...

If you are a Jazz employee please apply via the Internal Career site Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people ...

If you are a Jazz employee please apply via the Internal Career site Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people ...

The primary responsibilities of this position are to provide statistical consulting to clients in the biotech/pharmaceutical industry in their drug development programs with a focus on protocol/study design, analysis planning, and regulatory submission strategies. Provide statistical consult...

The primary responsibilities of this position are to provide statistical consulting to clients in the biotech/pharmaceutical industry in their drug development programs with a focus on protocol/study design, analysis planning, and regulatory submission strategies. Provide statistical consult...

The primary responsibilities of this position are to provide leadership in planning and conducting data analyses in clinical studies, and participate in planning and data analyses for regulatory submission. • Provide statistical consulting to clinical study design • Review study protocols and wr...

The primary responsibilities of this position are to provide leadership in planning and conducting data analyses in clinical studies, and participate in planning and data analyses for regulatory submission. • Provide statistical consulting to clinical study design • Review study protocols and wr...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000...

Greets patients, take appropriate vital signs, review current medications and record in medical record Assists with tracking and monitoring department specific data Provide clinical support, and ensuring the research trials compliance within research protocols Aid in the effective management of p...

Redwood City, CA (Hybrid)Corporate Strategy – Product Development /Full-time /HybridAbout KariusKarius is a venture-backed life science startup that is transforming the way pathogens and other microbes are observed throughout the body.  By unlocking the information present in microbial cell-free ...

The Clinical Trial Assistant (CTA) supports study teams in the planning, designing, executing, monitoring, and reporting of clinical trials. To assist project teams with trial progress tracking by updating the Clinical Trial Management systems. Clinical Trial Assistant in life sciences industry p...

Oversee data management activities including reviewing data management documents, data flow metrics, and driving data snapshot/closeout activities. The Clinical Data Manager will be responsible for daily data management tasks for all phases of clinical trials including CRO/vendor oversight and su...

Reporting to the Head of DM, this leader in Data Management will take ownership of a study in early development clinical trials. Lead data management activities from study startup through conduct and eventually closeout. Serve as in-house Data Management SME and collaborate with internal cross-fu...

Reporting to the Head of DM, this leader in Data Management will take ownership of a study in early development clinical trials. Lead data management activities from study startup through conduct and eventually closeout. Serve as in-house Data Management SME and collaborate with internal cross-fu...

The Clinical Program Manager in Clinical Operations Study Management will be responsible for overseeing the execution of clinical trials in oncology and other therapeutic areas, as required. ...

Director of Regulatory Submissions and Quality Monitoring. Coordinate w/ the PI & internal/external parties regarding the collection & maintenance of regulatory IRB & other documentation & procedures. At least 3 years of project management experience in clinical trials research or human subjects ...

Associate Director, Clinical Program Management *Hybrid Role - Redwood City, CA* Meet has partnered with an exciting biotech that is focused in the chronic illness space! They're very well-funded and have a strong mid-stage pipeline (multiple P1/2 trials). They are seeking an Associate Director o...

JOB TITLE: Senior Clinical Trial Specialist DEPARTMENT: Clinical Operations HIRING MANAGER: Lorna Dean LOCATION: South San Francisco, California / Remote (Hybrid) TYPE: Full-Time HI-Bio is a clinical-stage biotechnology company based in South San Francisco, California. Our shared purpose is to tr...

Provide technical, clinical, and educational support for all MicroVention products with the focus on new technologies. Provide didactic, hands-on, pre-clinical, clinical training, and case support to physicians, all hospital personnel, and customers as well as MV associates. Provide support for M...

Job Title: Clinical Contracts & Finance Manager- III* Location: Foster city, CA or NJ or Santa Monica, CA Duration: 12+ Months This is an onsite position 5 days a week. Candidate can be based in either FC or NJ or Santa Monica locations Description: Client is a research-based biopharmaceutical co...

About Us: Sagimet is a clinical-stage biopharmaceutical company developing novel fatty acid synthase (FASN) inhibitors that are designed to target dysfunctional metabolic pathways in diseases resulting from the overproduction of the fatty acid, palmitate. Sagimet’s lead drug candidate, denifansta...

Role Title: Director, Manufacturing, Science & Technology Department: Manufacturing Supervisor: COO and CEO FLSA: Exempt CORE VALUES Respect ● Passion ● Teamwork ● Integrity ● Honesty ● Commitment ● Collaboration FUNCTION SUMMARY Director, MSAT The Director of Manufacturing, Science, and Technolo...

... including clinical trials, stem cell transplants, transfusions, and other care delivery models ... Work with management to identify payer trends or potential issues * Demonstrate exceptional ...