- Abbott (Alameda, CA)
- …processes. This role is critical to the successful collection, reporting and analysis of clinical trial data as well as the mentorship of junior team members. ... 114,000 colleagues serve people in more than 160 countries. ** Clinical Data Manager ** **Working at Abbott** At...+ Develop and maintain Data Management Plans (DMPs) for clinical trials . + Develop edit check specifications… more
- J&J Family of Companies (Santa Clara, CA)
- …United States of America **Job Description:** Johnson & Johnson is hiring for a **Sr. Clinical Data Manager - Shockwave Medica** l to join our team. The position ... the treatment of calcified plaque. **Position Overview** The Sr. Clinical Data Manager is responsible for the...Knowledge and experience in supporting device pre- and/or post-market clinical studies, including IDE trials preferred. +… more
- Gilead Sciences, Inc. (Foster City, CA)
- … clinical study process improvements and SOPs. + Meets all requirements for Senior Clinical Trial Manager (Senior CTM) grade 28 position with demonstrable ... the worldwide execution of all Phase I - IV clinical trials across all Gilead therapeutic areas....global registration and commercialization of Gilead's products. As a ** Clinical Program Manager ** , you will oversee… more
- Abbott (Alameda, CA)
- …agreements (based on templates approved and provided by Legal) to ensure timely clinical trial start and compliance to internal and external regulations. + ... Negotiates Master Clinical Trial Site Agreements ("MCTSA"), Facility Use...terminology. Expertise with GCPs, and regulatory compliance guidelines for clinical trials (eg applicable ISO Standards, FDA).… more
- GRAIL (Menlo Park, CA)
- …medical device and/or pharmaceutical industry. + Prior experience leading mid to large scale clinical trials and ability to support multiple projects at a given ... For more information, please visit grail.com . The Senior Clinical Data Manager (CDM) will lead data...a state of constant audit-readiness and filed in the Trial Master File. + Create/review the Data Transfer Plan… more
- Abbott (Alameda, CA)
- …strategy implementation and operations for overseeing the direction, planning, execution, clinical trials /research and the data collection activities. + ... improve energy, lose weight or enhance athletic performance. The Clinical Affairs Manager will manage teams within...study design and costs. + Responsible for directing human clinical trials , for company products under development.… more
- BeOne Medicines (San Mateo, CA)
- …regular updates on study progress in the region to senior management and Global Clinical Study Manager as required + Represents the regional study team at ... study is operationally feasible in the region, drives trial feasibility, country allocation and site selection process for... Clinical Study Report in collaboration with Global Clinical Study Manager and Medical Writing **Quality:**… more
- Taiho Oncology (Pleasanton, CA)
- …design, conduct, monitoring and review of study data, analysis and reporting of clinical trials . Performance Objectives: + Collaborates with other key team ... Biomarkers and Medical Writing etc.), to deliver high quality clinical trial results. + Use scientific expertise...+ Keeps Sr. Medical Director current on status of clinical trials and provides ongoing risk assessments… more
- Terumo Neuro (Aliso Viejo, CA)
- …and resource allocation as it relates to data management. + Develop and implement clinical trial database, including CRF development and all aspects of data ... **12521BR** **Title:** Sr. Manager , Clinical Data Management **Job Description:** The Senior Manager , CDM oversees clinical data management activities… more
- Edwards Lifesciences (Sacramento, CA)
- …responsible for ensuring patient safety by overseeing the ethical conduct of clinical trials , maintaining strict regulatory compliance, and ensuring data ... on field monitoring of studies and data collection for clinical trials with increased volume and complexity...for consistency with case report form, and determine if clinical trial /study subject documentation is within parameters… more
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