Executive Assistant to CRO - Foster City

We are looking for a highly capable Executive Assistant to support our Chief Revenue Officer (CRO) and Chief Marketing Officer (CMO) at Replit. This role is ideal for an experienced EA who is ready to take on rapid organizational growth and act as a strategic partner to senior le ...

We are looking for a highly capable Executive Assistant to support our Chief Revenue Officer (CRO) and Chief Marketing Officer (CMO) at Replit. · This role is ideal for an experienced EA who is ready to take on rapid organizational growth and act as a strategic partner to senior ...

We are seeking an experienced Executive Assistant who has directly supported a CRO within a tech organization. · ...

The role will be responsible for the overall management and coordination of operational activities involved in the planning, conduct and completion of clinical trials including the management of deliverables, adherence to budget, and ongoing risk mitigation. · Bachelor's degree o ...

Clinical trials management associate with at least 3+ years of experience and a BS or BA in a relevant scientific discipline. Participates in meetings and conference calls with CROs, vendors, and multi-functional teams. Assists in CRO or vendor selection, coordinates CROs or vend ...

Sr. Clinical Trial Management Associate at Foster City, CA. · ...

This role will immediately assume biomarker data management responsibilities for representing biomarker data management at the biomarker Sub Team (BST) meetings. · ...

Clinical records associate with experience in maintaining clinical trial documentation and preclinical study records required. · Maintain an understanding of GCP, ICH and GLP regulations associated with the maintenance and retention of clinical trial documentation and preclinical ...

This role will immediately assume biomarker data management responsibilities for representing biomarker data management at the biomarker Sub Team (BST) meetings. The candidate will also be responsible for providing oversight to studies that fall within the BSTs. · ...

This role involves maintaining clinical trial documentation and preclinical study records following GCP, ICH and GLP regulations. · * Maintain an minimal understanding of GCP, ICH and GLP regulations associated with the maintenance and retention of clinical trial documentation an ...

We are seeking a highly motivated individual to join the Clinical Operations group. · This position reports into the Associate Director, Clinical Operations, · and is responsible for supporting the study team with study execution and providing logistical support in managing · the ...

We are seeking a highly motivated individual to join the Clinical Operations group. · We will have the opportunity to make a lasting impact at a company on the forefront of transforming oncology. · Assist in site selection activities · Manage assigned vendors to ensure that proje ...

Dice is the leading career destination for tech experts at every stage of their careers. Our client, NexInfo Solutions, Inc., is seeking a Clinical Trials Management Associate to assist in site selection and study implementation. · Provides administrative assistance in site selec ...

Provide input and assist with harmonization of Clinical Operations databases and tracking tools. · Assist in the maintaining clinical information and training of Clinical Operations personnel in the clinical trials database · ...

We are seeking a highly motivated individual to join the Clinical Operations group. This position reports into the Associate Director, Clinical Operations. · Working under the direction of the study lead(s), support global study by completing assigned tasks which include, but are ...

We are seeking a highly motivated individual to join the Clinical Operations group. This position reports into the Associate Director, Clinical Operations. · Working under the direction of the study lead(s), support global study by completing assigned tasks which include but are ...

Clinical Trials Management Associate · Provides administrative assistance in site selection, study implementation and ongoing coordination of study sites. · Monitors fairly routine study sites performing routine data collection source data verification. · ...

This is a QA Inspector position at Integrated Resources, Inc. · ...

+Gilead is creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and ensure access to these therapies across the globe. · +Lea ...

The Clinical Project Associate works under general supervision for routine tasks and with detailed instructions on new assignments. They must be familiar with FDA and EMA Regulations, ICH Guidelines, GCP, and standard clinical operating procedures. Excellent verbal and written co ...