Clinical Research Coordinator

Clinical Research Coordinator in Los Angeles, CA. Opportunity! This Jobot Consulting Job is hosted by: Robert Reyes Are you a fit? Easy Apply now by clicking the "Quick Apply" button and sending us your resume. Salary: $50 - $67 per hour A bit about us: Prestige Hospital System Advancing new knowledge and improving health outcomes through research Why join us? Competitive compensation Medical Insurance Dental Insurance Vision Insurance Life Insurance Flexible Schedule Job Stability Career growth If you are passionate, thrive in a fast-paced environment and are ready to take your career to the next level, we would love to hear from you. Job Details Job Details: We are seeking a dynamic and experienced Consulting Clinical Research Coordinator (CRC) to join our growing team in the healthcare industry. This role is instrumental in driving the success of diverse clinical trial types, including Phase I-IV Industry, NIH, and investigator-initiated Interventional and observational studies. The ideal candidate will have a strong background in clinical research and a proven track record of excellence in a senior or lead CRC capacity. Experience in academic medical centers, particularly UCLA/UCSF-type environments, will be highly advantageous. This role requires frequent interaction with sponsors, so comfort and experience in this area are essential. Responsibilities: As a Consulting Clinical Research Coordinator, your key responsibilities will include: 1. Overseeing and coordinating the daily activities of clinical trials to ensure compliance with protocol and overall clinical objectives. 2. Developing and implementing study-specific procedures, data collection systems, and research tools. 3. Collaborating with investigators to identify problems and provide solutions that ensure the integrity of research data. 4. Training and supervising clinical research staff to ensure they are performing their roles effectively and in compliance with study protocols. 5. Liaising with sponsors, investigators, and other stakeholders to ensure smooth communication and timely resolution of any issues. 6. Assisting in the preparation of regulatory submissions, progress reports, and other essential documents. 7. Participating in study design and protocol development, bringing your expertise to bear on the development of high-quality, efficient, and ethical clinical trials. Qualifications: To be considered for this role, you will need: 1. A minimum of 5 years of experience in a senior or lead CRC capacity, with demonstrated success in managing complex clinical trials. 2. Extensive experience across diverse trial types: Phase I–IV Industry, NIH, and investigator-initiated Interventional and observational studies. 3. Experience in academic medical centers, with a preference for UCLA/UCSF-type environments. 4. Exceptional communication skills and the ability to comfortably interact with sponsors, investigators, and other stakeholders. 5. Strong leadership and team management skills, with the ability to mentor and develop clinical research staff. 6. Excellent problem-solving skills, with the ability to identify and resolve issues in a timely and effective manner. 7. A strong commitment to ethical practices in clinical research, with a thorough understanding of regulatory requirements and guidelines. Join us as we continue to advance the frontiers of healthcare through clinical research. We look forward to reviewing your application. Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. 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