Operations Coordinator Salary at Echo Church BETA

*The ideal candidate for this role will reside in / near: Milpitas, Mountain View, Burlingame, San Carlos, Redwood City, Palo Alto or Sunnyvale California. *This role operates Tuesday - Saturday 8a-5p PST. Who We Are: At OPENLANE we make wholesale easy so our customers can be more successful. We’re a technology company building the world’s most advanced—and uncomplicated—digital marketplace for used vehicles. We’re a data company helping customers buy and sell smarter with clear, actionable insights they can understand and use. And we’re an innovation company accelerating the future of wholesale remarketing through curiosity, collaboration, and an entrepreneurial spirit. Our Values: Driven Waybuilders. We pursue challenges that inspire us to build, create and innovate. Relentless Curiosity. We seek to understand and improve our customers’ experience. Smart Risk-Taking. We transform risk into progress through data, experience, and intuition. Fearless Ownership. We deliver what we promis

Clinical Research Coordinator Overview As a Clinical Research Coordinator, you will lead the study team and be responsible for the execution of complex clinical trials from study design through study close out. You will be responsible for business and financial management of our research site, as well as oversight of day-to-day operations. Responsibilities Perform daily oversight and business management of all trials from start to study closure Coordinating, monitoring, and supervising all aspects of clinical studies from start-up to closeout, to ensure proper execution of assigned clinical research trials and to ensure that study protocols are me Preparing and maintaining administrative logs and trackers, including Regulatory Documents Collection tracker, eTMF tracker, Health Canada submission tracker, Central IRB Submission tracker, Site Shipments tracker, study visits, etc. Package, label, process, and ship specimen, filing and tracking of study visits, survey documents, including m

Clinical Research Coordinator Overview As a Clinical Research Coordinator, you will lead the study team and be responsible for the execution of complex clinical trials from study design through study close out. You will be responsible for business and financial management of our research site, as well as oversight of day-to-day operations. Responsibilities Perform daily oversight and business management of all trials from start to study closure Coordinating, monitoring, and supervising all aspects of clinical studies from start-up to closeout, to ensure proper execution of assigned clinical research trials and to ensure that study protocols are me Preparing and maintaining administrative logs and trackers, including Regulatory Documents Collection tracker, eTMF tracker, Health Canada submission tracker, Central IRB Submission tracker, Site Shipments tracker, study visits, etc. Package, label, process, and ship specimen, filing and tracking of study visits, survey documents, including m

Clinical Research Coordinator Overview As a Clinical Research Coordinator, you will lead the study team and be responsible for the execution of complex clinical trials from study design through study close out. You will be responsible for business and financial management of our research site, as well as oversight of day-to-day operations. Responsibilities Perform daily oversight and business management of all trials from start to study closure Coordinating, monitoring, and supervising all aspects of clinical studies from start-up to closeout, to ensure proper execution of assigned clinical research trials and to ensure that study protocols are me Preparing and maintaining administrative logs and trackers, including Regulatory Documents Collection tracker, eTMF tracker, Health Canada submission tracker, Central IRB Submission tracker, Site Shipments tracker, study visits, etc. Package, label, process, and ship specimen, filing and tracking of study visits, survey documents, including m

LEGARZA PROGRAM SPECIALIST - FULL TIME AND PART TIME POSITIONS AVAILABLE WHO ARE WE LOOKING FOR? The Legarza team is looking for a self-starter with a desire to be a part of a highly effective team, who is willing to go the extra mile in order to ensure success. We are in search of a motivated go-getter who has the skills and determination to develop, grow, and manage a phenomenal sports program. Someone that is meticulously organized and wakes up every morning with a passion to bring out the best in yourself and others. Someone who takes pride in being able to find creative solutions or bring order from chaos. As we continue to expand, we need a quality person who believes in our values and has the skills to implement, manage, and grow an extraordinary youth sports program. JOB DESCRIPTION: The job will require the talent to excite a group of children and will also mandate a professional approach in an office environment. You will inspire the next generation of leaders while running t

Clinical Research Coordinator Overview As a Clinical Research Coordinator, you will lead the study team and be responsible for the execution of complex clinical trials from study design through study close out. You will be responsible for business and financial management of our research site, as well as oversight of day-to-day operations. Responsibilities Perform daily oversight and business management of all trials from start to study closure Coordinating, monitoring, and supervising all aspects of clinical studies from start-up to closeout, to ensure proper execution of assigned clinical research trials and to ensure that study protocols are me Preparing and maintaining administrative logs and trackers, including Regulatory Documents Collection tracker, eTMF tracker, Health Canada submission tracker, Central IRB Submission tracker, Site Shipments tracker, study visits, etc. Package, label, process, and ship specimen, filing and tracking of study visits, survey documents, including m

Job Description: Overview: Serving as a full-time, embedded Operations Coordinator with a Fortune 50 Company in its corporate security organization, the selected candidate will be a high-visibility partner that leads the coordination and strategic alignment of activities that support diverse business functions. This position requires scrupulous attention to detail and the ability to operate at a tactical, and operational level. The primary focus of this position will be to coordinate scheduling, meetings, and activities assisting our client’s Regional Security Manager as they manage programs, people, and projects associated with a global corporate security program. The selected candidate will be responsible for providing administrative assistance, maintaining comprehensive and accurate records, organizing meetings, including scheduling, sending reminders, and managing calendars, including making appointments. This position requires curiosity, thoughtfulness, and a dedication to solving

Job Title: Clinical Research Coordinator I – Cardiovascular Research Location: Oakland Clinic and Pleasanton, CA (Onsite, East Bay, SF Bay Area) Position Type: 12-month contract About the Role: We are seeking 2-3 Clinical Research Coordinators (CRC I) to join our cardiovascular research team. This entry-level role is ideal for individuals passionate about clinical research and patient care, looking to make an impact in advancing cardiovascular health. The position will primarily be based onsite at our Oakland and Pleasanton clinics, supporting our ongoing clinical trials and studies. Key Responsibilities: Participant Recruitment: Conduct phone screening to recruit eligible patients and members for cardiovascular studies. Informed Consent: Obtain and document informed consent from study participants, ensuring understanding and compliance with study protocols. Clinical Measurements: Collect and record physical metrics, including height and weight, during participant visits. Data Entry: M