Assist in the planning, implementation, managing, and reporting of Phase I-III clinical studies. In collaboration with other clinical staff and/or an external CRO, monitoring clinical trial conduct/metrics (enrollment, GCP practices, handling of safety issues, etc.)
The candidate will use their immunology knowledge and will master the molecular immunological techniques including molecular cloning, retroviral transduction, siRNA, western blotting, immuno precipitation, PCR, RT-PCR.
The primary responsibilities include, but are not limited to: designing complex quantitative pathology assays, and implementing new technologies to address key questions about our therapeutic candidates.
The Clinical Coordinator plays a critical role in the successful implementation of telemedicine protocols for behavioral health patients in the emergency departments, inpatient units and in clinics at DHTN partner sites.
This position is responsible for completing analyses and developing manuscripts for cohort studies at the San Francisco Coordinating Center (SFCC), focused on clinical and translational research about aging.
The candidate will use their immunology knowledge and will master the molecular immunological techniques including molecular cloning, retroviral transduction, siRNA, western blotting, immunoprecipitation, PCR, RT-PCR.
This position will work closely with a cross-functional team to ensure that clinical trials are conducted in a timely fashion and in a manner compliant with SOPs, ICH/GCP/regulatory guidelines, company goals, and budgets.
As a Clinical Affairs Scientist, your main responsibilities will be to determine clinical strategy in conjunction with team members, write clinical protocols, analyze data and write reports to support the clinical documentation of Companion Diagnostics (CDx)in the field of tissue-based Cancer Diagnostics.
The Clinical Scientist will be a key contributor in building an integrated development plan in late development and will provide support to new development activities, as well as clinical guidance and assessment of future opportunities to advance the science and address unmet needs in oncology clinical development.
The Clinical Research Associate (CRA) conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Initiation, Routine Monitoring, and Close-out Visits.