Intake Coordinator

Description We are offering a short-term contract employment opportunity for a Clinical Research Coordinator in Walnut Creek, California. This role operates within the clinical research industry and involves analyzing, interpreting, and making decisions regarding protocol management for research protocols. Responsibilities: Analyze and interpret research protocols, making decisions regarding their management Evaluate protocol adherence, notifying relevant parties of deviations or violations Interact with monitors and sponsors to address and resolve study issues Conduct weekly team review meetings to provide insight on the clinical research process and team performance Train staff as needed and document these sessions Develop and update Unit Rules and Guidelines to ensure adherence to site SOPs Maintain an organized, efficient team environment Review and reconcile source documentation for accuracy such as medical history, medications, adverse events (AEs), etc. Update and maintain study enrollment logs and submit to the Sponsor as required Collect and review protocol forms and documentation to ensure accuracy Plan and execute workload for SIV/pre-study visits Make recommendations for patient recruitment activities Assist with reporting of serious adverse events (SAEs) Enter data into electronic case report forms (E-CRFs) or CRFs ensuring accuracy Maintain a high level of knowledge and understanding of the current study protocolSkills required include Research and Clinical Trial Operations.If you are interested, please apply and call us immediately at (510)470-7450Requirements Must possess a Bachelor's degree in a health-related field Should have a minimum of 2 years of experience in Clinical Research Profound knowledge of Clinical Trial Operations is essential Familiarity with Good Clinical Practice (GCP) guidelines is required Strong organizational skills and ability to manage multiple tasks concurrently Must have excellent written and verbal communication skills Proficient in Microsoft Office Suite Ability to maintain confidentiality of sensitive information Strong analytical skills and attention to detail Ability to work independently as well as in a team environment Must be willing to learn new processes and procedures High ethical standards and a commitment to scientific integrity Familiarity with electronic data management systems is a plus Must be able to travel as needed for study requirements. Robert Half is the world’s first and largest specialized talent solutions firm that connects highly qualified job seekers to opportunities at great companies. We offer contract, temporary and permanent placement solutions for finance and accounting, technology, marketing and creative, legal, and administrative and customer support roles.Robert Half works to put you in the best position to succeed. We provide access to top jobs, competitive compensation and benefits, and free online training. Stay on top of every opportunity - whenever you choose - even on the go. Download the Robert Half app (https://www.roberthalf.com/us/en/mobile-app) and get 1-tap apply, notifications of AI-matched jobs, and much more.All applicants applying for U.S. job openings must be legally authorized to work in the United States. Benefits are available to contract/temporary professionals, including medical, vision, dental, and life and disability insurance. Hired contract/temporary professionals are also eligible to enroll in our company 401(k) plan. Visit roberthalf.gobenefits.net for more information.© 2024 Robert Half. An Equal Opportunity Employer. M/F/Disability/Veterans. By clicking “Apply Now,” you’re agreeing to Robert Half’s Terms of Use (https:///www.roberthalf.com/us/en/terms) .