Study Coordinator Salary at Los Angeles Biomedical Research Institute BETA

Position: Research Associate - Administrative Location: 1000 Veteran Ave 32-59, LA 90095 Duration: 3 Months Shift 8:00 am - 5:00 pm includes a 60 min break Note: At least 1-2 year of study coordinator experience is required. Working hours - 8a-5p(M-F), On-site ONLY. SUMMARY STATEMENT The Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The position has responsibility for the implementation of research activities for one or more studies. The incumbent recognizes and performs necessary tasks to manage projects and prioritizes work to meet necessary deadlines. The incumbent is responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). The Clinical Research Coordinator collaborates w

Job Description Principal Investigator, Dr. Mustafa Khokha, MD, is looking for a Research Associate III to join the team! The Khokha Lab uses Xenopus, a frog model, to understand the molecular mechanisms that drive birth defects. The Research Associate will be responsible for managing the aquatics that house a colony of frogs which includes caring for adult frogs as well as rearing tadpoles to adulthood. Under general guidance, the Administrative Research Associate III works closely with PI, providing technical and/or administrative support in large or multi-project oriented labs. May be requested by PI to take on specific supervisory activities, and provide administrative leadership, and/or technical expertise. May develop hypothesis and assist in planning steps for the investigative process. Will review and remain current on literature as it relates to clinical/research study. Coordinates all lab and/or clinical activities, including but not limited to, budgetary/financial compliance

**Job Description** **Principal Investigator, Dr. Mustafa Khokha, MD, is looking for a Research Associate III to join the team!** Under general guidance, the Administrative Research Associate III works closely with PI, providing technical and/or administrative support in large or multi-project oriented labs. May be requested by PI to take on specific supervisory activities, and provide administrative leadership, and/or technical expertise. May develop hypothesis and assist in planning steps for the investigative process. Will review and remain current on literature as it relates to clinical/research study. Coordinates all lab and/or clinical activities, including but not limited to, budgetary/financial compliance, preparation of grant proposals, and creating independent presentations. Not responsible for generating grant funds. **What are the Primary Duties & Responsibilities?** + Provides miscellaneous clinical/research support (ad hoc data analysis, hypothesis development, programmin

Job Description Principal Investigator, Dr. Mustafa Khokha, MD, is looking for a Research Associate III to join the team The Khokha Lab uses Xenopus, a frog model, to understand the molecular mechanisms that drive birth defects. The Research Associate will be responsible for managing the aquatics that house a colony of frogs which includes caring for adult frogs as well as rearing tadpoles to adulthood. Under general guidance, the Administrative Research Associate III works closely with PI, providing technical and/or administrative support in large or multi-project oriented labs. May be requested by PI to take on specific supervisory activities, and provide administrative leadership, and/or technical expertise. May develop hypothesis and assist in planning steps for the investigative process. Will review and remain current on literature as it relates to clinical/research study. Coordinates all lab and/or clinical activities, including but not limited to, budgetary/financial compliance,

Job Description Job Description Matrix Clinical Research is a leading organization in the field of clinical research, dedicated to advancing medical knowledge and improving patient outcomes. We conduct cutting-edge research studies in various therapeutic areas, and we are looking for a dedicated Clinical Research Medical Assistant to join our dynamic team. Job Summary: The Clinical Research Medical Assistant will assist in the conduct of clinical trials by providing support to the clinical research team, ensuring the safety and well-being of study participants, and maintaining the integrity of study data. The ideal candidate is a detail-oriented professional with a passion for clinical research and patient care. Key Responsibilities: Assist in the recruitment, screening, and enrollment of study participants. Perform vital signs, ECGs, phlebotomy, and other clinical procedures as required by study protocols. Collect and process biological samples (e.g., blood, urine) for laboratory anal

Job Description Job Description Clinical Research Coordinator Location: Los Angeles, CA Travel: 50% travel required Experience: 2+ years in clinical trial coordination and regulatory compliance Job Overview We are seeking a dedicated and experienced Clinical Research Coordinator (CRC) to oversee the administration and coordination of industry-sponsored clinical trials across all protocol phases. This role requires strong expertise in regulatory compliance, IRB submissions, and clinical trial coordination. Strong adaptability and decision-making skills. Ability to comfortably work in a dynamic and high-volume clinical patient setting. Efficiently manage multiple tasks and prioritize efficiently. The ideal candidate will also have experience with investigational product (IP) handling, accountability, reconstitution, and destruction, as well as lab processing and specimen handling. Proficiency in Spanish is essential and phlebotomy skills required. A CMA certification is highly preferred.

About Us: Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k. Pay Range: $19.00 - $22.00/hr Working

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. As a Clinical Research Coordinator II, you will work independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. The incumbent will be responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. The CRC II member will be responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. The incumbent will present information at research staff