Clinical Research Coordinator Salary at The Parkinson's & Movement Disorder Foundation BETA

Job Description: Location: Los Angeles, CA (90033) Pay: $30 - $40/hour As the experienced Clinical Research Coordinator, you will work with a team that is dedicated to bringing quality care to those in the community who need it most. The majority of our patients are Hispanic, speak Spanish, and are diabetic. We work mostly in the diabetic wound care space, where we help patients find access to new treatments and devices so they can avoid amputations. The patients we support and provide care to are from under-served and minority populations that typically don’t get the focus they deserve. We are on a mission to fix that. We work on both federally and privately funded studies. As a member of the team, you will: Collaborate with our team of clinical research coordinators Work closely with renowned doctors and researchers Work with our doctors across multiple clinics to help recruit, screen, and enroll patients Review and comprehend study protocols Help with patient scheduling and follow-u

Job Description Primary Duties and Responsibilities The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for study and assist with study budget and patient research billing. Ensures compliance with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care. Primary Duties and Responsibilities Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study. Evaluates and abstracts clinical research data from source documents. Ensures compliance with protocol and overall clinical research o

Job Description Job Description Summary NRC Research Institute is seeking a full-time and part-time Clinical Rater for its Los Angeles, CA research site. The individual will regularly collaborate with Psychologists, Psychiatrists, Clinical Research Coordinators, Medical Monitors, and Pharmaceutical representatives. The Clinical Rater will be instrumental in the planning, implementation, coordination, and execution of activities associated pharmaceutical development. Job Responsibilities The Clinical Rater will administer various clinical efficacy scales on different patient populations, such as ADHD, Alzheimer’s disease, Bipolar Disorder, Major Depressive Disorder, Schizophrenia, etc. The Clinical Rater will follow guidelines set forth by study protocols written by various pharmaceutical companies. The Clinical Rater will write elaborate psychological in-take reports to document and confirm a DSM-5 diagnosis by utilizing data points from clinical efficacy scales. In addition, the Clini

Description: Provide leadership in the planning, development, and implementation of program plans for all initiatives instituted by RD. Provide leadership in program operations and administrative functions including budget and business transactions, outreach and marketing, and dissemination. Serves as key contact and resource for RD program information within SC CTSI and its partners. Ensure participants and teams are informed and have access to available tools, materials, and resources. Track and monitor SC CTSI-sponsored research team progress and work with RD leadership to ensure appropriate processes are in place and interventions occur when needed. Communicate and promote new team science tools and activities; track and prompt participation for follow-up through all phases. Requirements: 1+ year of experience or combined education/experience as substituted for minimum experience in directly related field of administrative support services and either clinical, basic, and/or populat

CARE Institute is a start-up company firmly established in the research industry. We provide quality clinical research that significantly impacts the health of patients and communities. Our mission is to advance scientific and medical knowledge within the industry. The clinical research coordinator (CRC) is responsible for all aspects of the clinical trial, ensuring trouble-free running of all clinical trials. This is not limited to one trial at a time. The CRC will be monitoring the study to ensure that it complies with protocols, is ethically conducted and follows regulatory standards. The CRC will work with the Recruitment Specialist and Regulatory Specialist in completing all forms, procedures, and compliance for each trial. Attention to detail and organizational skills are essential for success in this role. Responsibilities: Supervise the daily activities of a study and monitor the activities of the subjects and researchers Perform various medical procedures including patient vit

**Job Description** **Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements!** Work alongside physician-scientists and researchers who are making life-saving medical and scientific breakthroughs. Our team of scientists develop some of the most advanced clinical trials in the world. The Clinical Research Coordinator I will work independently providing study coordination, screening of patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. This position is responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. The incumbent will be responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. The CRC I member will present study information at research staff meetings and ensur

Job Description: As the experienced Clinical Research Coordinator, you will work with a team that is dedicated to bringing quality care to those in the community who need it most. The majority of our patients are Hispanic, speak Spanish, and are diabetic. We work mostly in the diabetic wound care space, where we help patients find access to new treatments and devices so they can avoid amputations. The patients we support and provide care to are from underserved and minority populations that typically don’t get the focus they deserve. We are on a mission to fix that. We work on both federally and privately funded studies. As a member of the team, you will:: Collaborate with our team of clinical research coordinators Work closely with renowned doctors and researchers Work with our doctors across multiple clinics to recruit, screen, and enroll patients Review and comprehend study protocols Coordinate and attend monitor site visits and prepare site visit documentation Ensure study staff is

Job Description Job Description Job Description: Clinical Research Coordinator (CRC) – Phlebotomist or Medical Assistant SeraCollection Research Services is seeking experienced Phlebotomists and Certified Medical Assistants for Clinical Research Coordinator (CRC) positions. This is an excellent opportunity to advance your career in clinical research. Position Overview: All Phlebotomists and Medical Assistants will receive comprehensive training to become Clinical Research Coordinators, including certification in Good Clinical Practices (GCP) and Shipping of Dangerous Goods (IATA). While prior experience in medical research is not required, it is highly recommended. Our work involves high-risk patients and infectious diseases, including COVID-19. Full PPE is provided to ensure safety. This role involves more than just blood draws — you will also work closely with the CRC Lead to manage and organize research-related documentation, file paperwork, and input data accurately into clinical s