Clinical Research Coordinator

Overview Clinical Research Coordinator | Temp to Hire | Salary: $70,000 - $75,000 per year. Position hosted by Jobot Consulting (onsite in Fountain Valley, CA, M-F; hybrid not available). Fluency in English and Spanish is required. About the role We are seeking an experienced Consulting Clinical Research Coordinator to join our healthcare team. This role involves managing and overseeing clinical trials, ensuring studies are conducted in accordance with ethical standards and regulatory requirements, and contributing to groundbreaking research in Gynecologic Oncology (GynOnc). Why join us? Medical, Dental and Vision Insurance 401K with Match Temp to Hire opportunity PTO and Sick PTO And more Job Details Bachelor's degree in a related field preferred 3+ years of experience in clinical research coordination Prior experience in Gynecologic Oncology (GynOnc) is a plus Excellent knowledge of clinical trial design, management, and regulatory requirements Strong understanding of Good Clinical Practice (GCP) guidelines Exceptional organizational skills and ability to manage multiple clinical trials simultaneously Excellent communication and interpersonal skills Proficient in using clinical trial management systems and related software Ability to work effectively in a team and independently Detail-oriented with strong problem-solving skills Proven ability to maintain confidentiality and handle sensitive information with discretion Willingness to stay updated on trends and developments in GynOnc Commitment to improving patient care and treatment outcomes through clinical research Note: Fully onsite (M-F) at Fountain Valley, CA; hybrid not available Responsibilities Oversee day-to-day management of clinical trials, including patient recruitment, data collection, and data analysis Ensure trials are conducted per study protocol, ethical standards, and regulatory requirements Coordinate with physicians, nurses, and other healthcare professionals to ensure patient safety and data integrity Develop and maintain relationships with study sponsors, investigators, and key stakeholders Prepare and submit regular reports on study progress and results Participate in development of study protocols, informed consent forms, and case report forms Identify, evaluate, and manage potential risks and issues related to clinical trials Provide training and guidance to other members of the clinical research team Stay updated on trends and advancements in GynOnc Application notice Interested in hearing more? Easy Apply now by clicking the "Easy 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, disability, military status, genetic information or any other basis protected by applicable laws. Jobot may perform background checks with authorization and may consider candidates with criminal histories in a manner consistent with applicable laws. For information on privacy, see Jobot’s Privacy Policy and related notices. #J-18808-Ljbffr