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Last updated: 1 day ago $105,000.00 yearly Full-time Clinical Research Site Manager.At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities.As a leading network of advanced clinical trial sites, we leverage... Show more $135,000.00 yearly Full-time Clinical Research Site Leader/Chief Operating Officer.Requisition Number: CLINI003092.Location: CIT Riverside, CenExel CIT, 5700 Division Street, STE 101, Riverside, CA 92506, USA.Each of CenExel's... Show more Full-time Licensed Clinical Psychologist (Ph.CHE Behavioral Health Services.Licensed Clinical and Counseling Psychologists to join our APA-approved, clinician-led behavioral health team.CHE has been a nation... Show more $110,000.00 yearly Full-time We are searching for a Child and/or Adult Clinical Psychologistto provides clinical services including psychological assessments and individual, family, multi-family, couples, and group therapy, b... Show more Full-time The Department of Biochemistry and Molecular Biology studies how biomolecules function and interact to drive the complex, diverse, and adaptive behaviors of living systems.Our focus is on biologica... Show more Full-time Shared Services: Human Research Protection Program (Full-Time, Day Shift, Hybrid/Remote) -.Our mission is to continue the teaching and healing ministry of Jesus Christ.Our core values are compassio... Show more $95,000.00 yearly Full-time Loma Linda University Faculty Medical Group, Department of Pediatrics,and The Inland Empire Autism Assessment Center of Excellence (AAC) are seeking a pediatric neuropsychologist/pediatric psychol... Show more $34.17 hourly Full-time +1 College of Natural & Agricultural Sciences.Qualifies for Employee Referral Bonus: No.The Research Administrator 2 (RA) will provide direct support in pre- and post-award administration for the assi... 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Show more $15.00 hourly Part-time +1 Product Testers are wanted to work from home nationwide in the US to fulfill upcoming contracts with national and international companies.We guarantee 15-25 hours per week with an hourly pay of bet... Show more Full-time Great employees deserve great benefits!.Paid vacation 3 weeks per year.Medical, dental, vision, and life and disability plans.Sick time and company holidays.Leave programs for qualifying events.Eli... Show more The cities near Rialto, CA that boast the highest number of psychologist research assistant jobs are: Moreno Valley San Bernardino Riverside Menifee The 10 cities near Rialto, CA that have the most job openings are: Victorville Pomona Corona Rancho Cucamonga Ontario Fontana Moreno Valley San Bernardino Riverside West Covina The 10 most popular job searches in Rialto, CA are: amazon government warehouse work from home amazon warehouse construction security amazon flex factory worker truck driving At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion. The Site Manager performs clinical research activities as a Clinical Research Coordinator while also serving as Manager of the site operations. The Site Manager owns meeting or exceeding financial targets, KPIs, and patient enrollment, as well as champions screening, patient retention, and partnering with other Headlands centralized departments or sites. Position Type: Full-time Location: Onsite in Riverside, CA Responsibilities: Strategic and Operational Management Evaluates overall performance of the Site and recommends and implements processes and plans for improvement. Responsible for maintaining a site calendar to ensure adequate enrollment for studies and coordination of employee PTO. Staff Development and Management Fosters a culture of excellence, teamwork, and innovation among site staff Hires, trains, and mentors site staff, including Clinical Research Coordinators, Research Assistants, Administrative Assistants, Registered Nurses, support personnel, etc. Partners with Human Resources and Management when hiring new employees for the site by reviewing candidate credentials, conducting interviews, and giving input about potential new hires Supervises performance of other Clinical Research Coordinators, Research Assistants, and support staff at the Site Quality Assurance & Compliance Maintains up-to-date knowledge of all relevant regulatory guidelines and requirements Ensures the site's compliance with FDA, ICH, and local regulatory agency regulations Clinical Research Coordination In addition to assuming management responsibilities as a Site Manager, this individual performs the duties of a Clinical Research Coordinator Protects the rights, safety, and welfare of human subjects, follows Good Clinical Practice, and works cooperatively with others Monitors study activities to ensure compliance with study protocols, with site policies, and with applicable federal, state, and local regulations Oversee the planning, initiation, and execution of clinical trials at the site Maintains required records of study activity including case report forms, drug dispensation records, and regulatory forms Manages and optimizes patient recruitment and retention efforts Assesses eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and other healthcare professionals Addresses any patient concerns or issues promptly and professionally Documentation and Reporting Documents findings and events in the CTMS platform and in other binders and platforms as directed Reviews proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks Performs other duties as assigned, including duties routinely performed by the Company's Research Assistants Requirements: 5+ years of experience as a delegated Clinical Research Coordinator on multiple phase 2-4 clinical research trials, simultaneously Proficiency in FDA regulations governing clinical trials Strong supervisory skills to lead research staff effectively Ability to collect and manage research data accurately Familiarity with documentation review processes in clinical research Knowledge of medical terminology relevant to clinical trials management GCP (Good Clinical Practice) Strong communication skills with all members of the team. Preferred Qualifications: Capability to perform phlebotomy procedures CCRC or CCRP certified $100,000 - $105,000 USD Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind. Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. #J-18808-Ljbffr