Clinical Site Monitor - Los Angeles, CA

The oversees the New Beginning's Program participants' activities and ensuring compliance with program rules and expectations. This position helps maintain smooth and consistent facility and residence operations. · ...

The Site Monitor is responsible for overseeing program participants and ensuring compliance with program rules and expectations. · Minimum high school diploma or equivalency, associate degree in social services preferred · One - two years' experience in behavioral health or soci ...

The Site Monitor oversees participants' activities in an interim housing program for individuals experiencing homelessness. The role involves maintaining smooth facility operations while assisting clients in overcoming barriers to recovery. · Performs duties as prescribed by esta ...

The Site Monitor oversees the New Beginning's Program participants' activities and ensuring compliance with program rules and expectations. · ...

The Client Support Specialist at The Village at Midvale plays a critical role · Foster a calm, respectful, and welcoming environment. · Support the overnight operations of the site. · ...

We are currently seeking a Senior Clinical Research Associate to join our diverse and dynamic team.As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requir ...

The Oversight Monitor provides independent oversight of clinical monitoring activities conducted by Contract Research Organizations (CROs) and third-party vendors. · ...

The Oversight Monitor provides independent oversight of clinical monitoring activities conducted by Contract Research Organizations (CROs) and third-party vendors. · ...

The Site Administrator is responsible for successfully managing day to day operations of all Martin Luther King Community Medical Group sites. Provides physicians and allied health professionals resources required to meet patient needs and meet the strategic and financial objecti ...

+h2>Job summary · The Clinical Research Associate supports clinical trial execution by independently monitoring study sites and ensuring compliance with protocol GCP and regulatory requirements. · Perform site qualification initiation monitoring and close-out visits · Review sour ...

The Clinical Research Associate will work on multiple trials within the Cross Therapeutic areas - Start up focus. · ...

+ The Site Administrator is responsible for successfully managing day to day operations of all Martin Luther King Community Medical Group sites. · ...

+We are seeking a Clinical Research Associate to join our team in Los Angeles. The successful candidate will be responsible for conducting site visits and ensuring compliance with ICH-GCP and regulations.+ · ++• Serve as the primary point of contact between investigational sites ...

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. · Oversee and manage clinical trial activities. · Ensure data integrity, participant safety, and compliance throughout the study lifecycle. · ...

The Operations Manager Shelter Services role provides day-to-day oversight of shelter monitors and security staff across multiple Interim Housing Inside Safe shelter sites. · This hands-on leadership position supervises more than 50 shelter monitors security staff operating acros ...

+ Bioremediation Field Technician · CAER is seeking two Field Bioremediation Technicians to support hands-on field implementation and monitoring of bioremediation projects.This role is ideal for someone who enjoys outdoor, physically active work and is interested in applied envir ...

Senior MEP Inspector. · Visits construction sites and inspects each stage of construction up to completion. · Maintains daily activity logs and reports. · ...

Clinical Research Associate - Oncology - Los Angeles, CA ICON plc is a world-leading healthcare intelligence and clinical research organization. · Serve as the primary point of contact between investigational sites and the sponsor · ...

· This ​jobs requires a Sr. · a Bachelor's degree from an accredited university or college. · a superb understanding of all aspects of clinical research. · a minimum five years clinical research experience. · demonstrated strong written and verbal communication skills with inter ...

Clinical Research Associates work with healthcare organizations to oversee the execution of clinical trials and ensure compliance with ICH-GCP regulations. · ...