- Parexel (Sacramento, CA)
- …Participate in the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), integrated clinical and statistical ... to MMP during the study conduct + Answer to site / study team questions relating to the study conduct...appropriate for the MD + Providing risk assessment of clinical trials for local sponsorship as needed with the… more
- Abbott (Pleasanton, CA)
- …supervision of senior colleague/ manager (or delegate), the Associate Clinical Site Lead drives study execution and operational excellence across Abbott ... indication of trends, clinical trial enrollment, and ICH-GCP and clinical research application. Adheres to specified site nomination, qualification, and… more
- Edwards Lifesciences (Irvine, CA)
- …longer and healthier lives. Join us and be part of our inspiring journey. As the Senior Analyst, Clinical Trials & Site Contracts, you will be responsible ... expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of...EW policies and procedures + In Collaboration with the Manager , initiate and maintain the Financial Score Card and… more
- BD (Becton, Dickinson and Company) (Irvine, CA)
- …your best self. Become a **maker of possible** with us. We are seeking a ** Senior Manager , Clinical Affairs** to lead strategic initiatives within our ... direction on field and remote monitoring of studies and data collection for all clinical trials, act as a study project manager , assess all data documentation,… more
- GRAIL (Menlo Park, CA)
- …technology, and healthcare companies. For more information, please visit grail.com . The Sr. Clinical Trial Manager serves as a clinical operations leader, ... + Manages all clinical operational aspects of a clinical trial from site selection, start-up, enrollment, maintenance, and close-out + Develops study related… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …to join the Clinical Operations team based in Santa Monica as a Senior Clinical Trial Manager , specializing in Late Phase studies. **Essential Duties ... and guidance for global late phase studies* Coordinates review of interim/final clinical study reports.* Ensures effectiveness of site budget/contract processes… more
- Bristol Myers Squibb (San Diego, CA)
- …the global leader in radiopharmaceuticals . We are seeking an experienced ** Clinical Medical Writer** with strong project management capabilities to join our growing ... clinical development team. This hybrid role combines the scientific...experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location.… more
- BeOne Medicines (San Mateo, CA)
- **General Description:** + Focusing mainly on the Depot storage, site distribution, drug return & destruction and logistics related Depot performance management in ... data calculation and reporting. + Coordinate or directly organize site to site transfer shipments as needed....Depot vendor's performance and report Depot metrics (KPIs) to senior management. + Ensure the requirements and business process… more
- Pfizer (South San Francisco, CA)
- …study level informed consent documents, and contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other ... responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for...requiring you to live within commuting distance and work on- site an average of 2.5 days per week. The… more
- Kelly Services (Irvine, CA)
- **Summary:** The Senior Clinical Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department ... relationships with colleagues across the organization. **Responsibilities:** + Serve as a Senior Clinical Research Specialist within the Clinical R&D… more
