- Edwards Lifesciences (Los Angeles, CA)
- …Bachelor's Degree and a minimum of 5 years of work experience in clinical research monitoring, with a strong focus on quality assurance, quality control, ... Knowledge of cardiovascular physiology and structural heart anatomy + Previous medical device Clinical Research experience in cardiology + Clinical … more
- Taiho Oncology (Pleasanton, CA)
- …trial results. + Use scientific expertise to support the creation of relevant high- quality clinical documents such as study protocols and clinical study ... treatment and improving patients' lives. As a Senior Manager, Clinical Research Scientist, you will play a...development industry in oncology and with previous exposure to clinical development, such as reviewing of the quality… more
- Parexel (Sacramento, CA)
- …candidates based in the Midwest, West Coast, Northeast & North Carolina The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, ... credibility, scientific leadership and in order to facilitate their clinical development goals + Support the study...+ Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years… more
- ManpowerGroup (Sunnyvale, CA)
- **Title:** Clinical Research Associate (CRA) **Location:** Sunnyvale, CA **Duration:** 12 Months **Pay Range:** $45 to $50/hr We are looking for an **Internal ... Clinical Research Associate (CRA)** to join one...Review and ensure accurate reporting of adverse events. + Support subject enrolment, recruitment, and retention efforts. + Prepare… more
- Swedish Health Services (CA)
- **Description** **Remote Position** The Clinical Research Budgets Analyst will be responsible for the timely and accurate preparation and maintenance of budget ... time **Job Shift:** Day **Career Track:** Business Professional **Department:** 3909 SRE CLINICAL TRIALS RESEARCH **Address:** WA Seattle 801 Broadway **Work… more
- IQVIA (Carlsbad, CA)
- …in lieu of degree. Req * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... manage ongoing project expectations and issues. * Evaluate the quality and integrity of study site practices related to...and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- Parexel (Glendale, CA)
- …their safety and wellbeing. Develop professionally by gaining experience in delivering high- quality research projects in this growing sector. **What you'll do ... after training is completed (including but not limited):** + Support Standard Operating Procedures (SOPs), Good Clinical Practices (GCP), and all work processes… more
- BeOne Medicines (Emeryville, CA)
- …a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance ... with general and study-specific monitoring issues * Provide direct support to the Clinical Study Manager by...through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery… more
- Astellas Pharma (San Diego, CA)
- …The Site Manager will manage the site/sponsor relationship as it relates to clinical trial delivery through consistent communication and support . The Site ... ** Clinical Site Manager - Southern California** Do you...CSM for specific study providing study level oversight and support for CSMs assigned to the study. This assignment… more
- Medtronic (CA)
- …marketing materials. + Collaborate with cross-functional teams, such as marketing, sales, clinical , R&D, HE&R, Quality , Compliance and Regulatory, and may ... exciting role you will have primary responsibility for leading and developing clinical , scientific, and regulatory documents while working in a cross-functional team… more