Clinical Trial Management - Los Angeles

The Project Manager (PM) for the Division of Clinical Trials Development (CTD) supports clinical research efforts at UCLA and within the TRIO-US Network. · ...

We're here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have chang ...

The Clinical Trails Manager is responsible for managing the activities of several clinical studies including assisting in the development of study-related documents, study site management, and patient data monitoring. This position works on site in El Segundo, CA or remotely depe ...

· About RDI · RDI is a tech-enabled Contract Research Organization (CRO) focused on diagnostic and sample-centric clinical studies. We partner with leading IVD and life sciences companies when studies need to be executed with precision, speed, and operational rigor. · We are bui ...

Clinical Trails Management Associate - III role involves conducting site evaluations/initiations and closeout visits in addition to routine monitoring visits. The candidate must meet all requirements for Clinical Research Associate position. · ...

We are seeking an experienced Clinical Trials Management Associate to support the planning coordination and execution of clinical trials for a high-profile client. · Ensure regulatory compliance data quality and efficient collaboration with CROs vendors and internal teams. · ...

Se busca un Clinical Trials Management Associate para una client muy importante. · ...

The Clinical Trials Management Associate - III is a senior-level clinical operations role responsible for independently managing and supporting routine clinical trial activities with limited supervision. · This role ensures site compliance, data integrity, and adherence to regula ...

+ Clinical Trials Management Associate - III* · Location: Santa Monica, CA · + Specific Job Responsibilities: Assures site compliance with the routine protocol and regulatory requirements and quality of data. + Travel is required + Excellent verbal, written, interpersonal and p ...

As a Clinical Trials Management Associate III at LeadStack Inc., you will lead site evaluations/initiations and closeout visits in addition to routine monitoring visits. · ...

Join Net2Source Inc. as Clinical Trials Management Associate - III and contribute to routine clinical trial activities with limited supervision. · Conduct site evaluations and monitoring visits ...

The Senior Clinical Trial Manager is responsible for the successful execution of clinical trials from protocol concept to completion. · Manages all clinical aspects of a study. · Assesses operational feasibility and manages comprehensive study timelines and metrics. · Participate ...

We are seeking an experienced Clinical Trials Management Associate to support the planning, coordination, and execution of clinical trials for a high-profile client. · Conduct site evaluations, initiations, monitoring, and close-out visits · Ensure protocol, regulatory, and data ...

We are seeking a Clinical Trials Management Associate for a very important client. · Working knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of routine clinical trials · Assures site compliance with the routine protocol and regulatory requ ...

LeadStack Inc. is an award-winning, one of the nation's fastest-growing, certified minority-owned (MBE) staffing services provider of contingent workforce. · ...

We are hiring Clinical Trials Management Associate for one of our clients. · We offer consulting solutions customized to our 450+ clients ranging from Fortune 500/1000 to Start-ups across various verticals like Technology, · Financial Services, Healthcare, Life Sciences, Oil & Ga ...

The Senior Clinical Trial Manager (Senior CTM) is responsible for the successful execution of clinical trials from protocol concept through clinical study report.The Senior CTM ensures completion of study deliverables typically works on studies with moderate to high complexity in ...

+Job summary · Puma Biotechnology Inc. is seeking a Senior Clinical Trial Manager to oversee the execution of clinical trials from protocol concept through clinical study report. · +ResponsibilitiesManages all clinical aspects of a study. · Assesses operational feasibility and st ...

+4 years of experience and a BS or BA in a relevant scientific discipline · Must meet all requirements for Clinical Research Associate position and have demonstrated proficiency in all relevant areas. · Specific Job Responsibilities: · Assures site compliance with the routine pro ...

The Senior Clinical Trial Management Specialist is responsible for the planning execution and oversight of clinical trials in compliance with regulatory requirements ICH-GCP guidelines and company SOPs.This role involves cross-functional collaboration vendor and CRO oversight sit ...