Physician Lead in Neuroscience Clinical Trials - Pomona - beBeeClinicalResearcher

Clinical Trial Physician (Neurologist) - 8 hours per week · Location: Pomona, CA · Schedule: Flexible Part-Time (0-8 hours per week) · Start Date: Within 0-6 months · Position Summary · We are seeking a board-certified Neurologist to serve as a Principal Investigator (PI) or Sub- ...

We are looking for a Clinical Trials Associate to support device processes associated with clinical trials. · Ensure compliance with regulations and manage the lifecycle of device inventory and accountability to support clinical trials. · Partner with stakeholders to manage inven ...

We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · Various annual leave entitlements · A range of health insurance offerings to suit you and your family's ne ...

We are looking for a Clinical Trials Associate (CTMS/eTMF) to support device processes associated with clinical trials. The successful candidate will ensure compliance with regulations and manage the lifecycle of device inventory and accountability to support clinical trials. · E ...

RDI is a tech-enabled Contract Research Organization (CRO) focused on diagnostic and sample-centric clinical studies. · ...

RDI is a tech-enabled Contract Research Organization (CRO) focused on diagnostic and sample-centric clinical studies. · ...

We are looking for a Clinical Trials Associate You will support device processes associated with clinical trials and ensure compliance with regulations. · ...

We are looking for a Clinical Trials Associate to support device processes associated with clinical trials and ensure compliance with regulations. · Partner with stakeholders to manage inventory and device accountability for sites. · Evaluate clinical study documents and perform ...

The Clinical Trail Management Associate assists the Sr. Clinical Trail Management Associate in the operational execution of assigned clinical studies. The employee must conduct their work activities in compliance with all relevant laws and regulatory guidelines as well as all *** ...

The Clinical Trial Manager (CTM) is responsible for the oversight and management of all clinical operational activities at the trial and site level. · ...

+Clinical Trial Manager · Job summary: · We are hiring Clinical Trial Manager for one of our clients. · +Benefits:Visa Sponsorship is currently not available for this role · ...

We are builders of clinical trials at the intersection of clinical operations, laboratory execution and regulatory discipline. · Lead diagnostic and sample-centric studies from startup through closeout · Own timelines, deliverables and cross-functional coordination · ...

Clinical Project Manager at ICON plc. Manage and lead cross-functional trial teams to ensure completion of assigned trials according to established project team goals and objectives. · Manage day-to-day operations of assigned trials. · Lead cross-functional trial teams including ...

Clinical trial lead at ICON plc, a world-leading healthcare intelligence and clinical research organization. · ...

RDI is a tech-enabled Contract Research Organization (CRO) focused on diagnostic and sample-centric clinical studies. · Lead diagnostic and sample-centric studies from startup through closeout · Own timelines, deliverables, and cross-functional coordination · ...

We are hiring Clinical Trial Manager for our client.We offer a wide gamut of 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, · ...

We are looking for a Clinical Trials Associate to support device processes associated with clinical trials. You will ensure compliance with regulations and manage the lifecycle of device inventory and accountability. · Bachelor's Degree in a related field with a minimum of 1 year ...

The Systems, Analytics and Reporting Associate (CTMS) are responsible for global investigator payment setup and other CTMS related support activity. · The employee in this position will have excellent organizational skills, good computer skills, flexibility, attention to detail, ...

+This position will be in based onsite in Irvine, California with no travel. · Provide support in quality oversight of the TMF for studies within and across programs · Partner with study teams to support the adoption of processes and standards, · Provide TMF industry expertise to ...

National Institute of Clinical Research is seeking an experienced Clinical Trial Participant Recruitment Manager to lead participant recruitment and retention strategies across clinical research studies. · ...

The Clinical Trial Registries Associate is a member of the Global Clinical Trial Registries Team within Business Operations, part of Drug Development Operations. · Provide support in quality oversight of the Registry health for studies within and across programs · Contribute to R ...