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Experienced Clinical Research Coordinator Jobs in Nevada

Clinical Research Coordinator Jobs
By Phoenix Children's Hospital At , Phoenix
Creates study budgets and works with management to determine financial feasibility and resources necessary to conduct the trial
Reviews all regulatory requirements to ensure implementation of appropriate methods, practices, and procedures for all research activities in designated area
With the principal investigator, explains the study purpose, parameters, and requirements of the studies to the participants
Completes case report forms, data entry, and maintains source documentation for all study participants
Offering the most comprehensive care across ages, communities and specialties
Advancing education and training to shape the next generation of clinical leaders
Clinical Research Coordinator Jobs
By Medasource At Manhattan, NY, United States
1+ years of Clinical Research Coordination experience
Resilient in recovering from setbacks and skilled at finding detours around obstacles.
Ensure data quality and integrity throughout the life of the study.
Collaborate with members of the research and care teams across MSK regarding data input.
Generate data reports and deliver to all necessary parties on the progress of the research project, database, or protocol.
Ensure all appropriate Institutional, State, and Federal regulations throughout the study are followed.
Clinical Research Coordinator - Twain
By Comprehensive Cancer Centers of Nevada At Las Vegas, NV, United States
Participates in required training and education programs. Responsible for education of clinic staff regarding clinical research
Additional responsibilities may include working directly with other research bases and/or sponsors
Minimum one (1) year of medical office experience, oncology or clinical research preferred
SoCRA or ACRP certification preferred
Collaborates with physicians in determining the eligibility of patients for clinical trials
Responsible for accurate and timely data collection, documentation, entry, and reporting. Schedules and participates in monitoring and auditing activities

Are you an experienced Clinical Research Coordinator looking for a new challenge? We are looking for a motivated individual to join our team and help us conduct clinical research studies. You will be responsible for coordinating all aspects of the clinical research process, from protocol development to data collection and analysis. If you have a passion for clinical research and are looking for an exciting opportunity, this is the job for you!

Overview Experienced Clinical Research Coordinators are responsible for managing and coordinating clinical research projects. They are responsible for ensuring that all research activities are conducted in accordance with applicable regulations and guidelines. They must be knowledgeable in clinical research protocols, regulatory requirements, and Good Clinical Practice (GCP). Detailed Job Description Experienced Clinical Research Coordinators are responsible for the planning, implementation, and management of clinical research projects. They must ensure that all research activities are conducted in accordance with applicable regulations and guidelines. They must be knowledgeable in clinical research protocols, regulatory requirements, and Good Clinical Practice (GCP). They must be able to effectively communicate with research staff, sponsors, and other stakeholders. They must be able to develop and maintain effective working relationships with research staff, sponsors, and other stakeholders. Job Skills Required
• Knowledge of clinical research protocols, regulatory requirements, and Good Clinical Practice (GCP)
• Excellent communication and interpersonal skills
• Ability to develop and maintain effective working relationships with research staff, sponsors, and other stakeholders
• Ability to manage multiple projects simultaneously
• Ability to work independently and as part of a team
• Strong organizational and problem-solving skills
• Proficiency in Microsoft Office Suite
Job Qualifications
• Bachelor’s degree in a related field
• At least 3 years of experience in clinical research
• Certification in Clinical Research Coordination (CCRC) or Clinical Research Associate (CRA)
Job Knowledge
• Knowledge of clinical research protocols, regulatory requirements, and Good Clinical Practice (GCP)
• Knowledge of clinical trial design, data management, and statistical analysis
• Knowledge of medical terminology and clinical terminology
• Knowledge of medical ethics and patient privacy regulations
Job Experience
• At least 3 years of experience in clinical research
• Experience in clinical trial design, data management, and statistical analysis
• Experience in developing and managing clinical research projects
• Experience in working with sponsors and other stakeholders
Job Responsibilities
• Develop and manage clinical research projects
• Ensure that all research activities are conducted in accordance with applicable regulations and guidelines
• Develop and maintain effective working relationships with research staff, sponsors, and other stakeholders
• Monitor and report on the progress of clinical research projects
• Prepare and submit reports to sponsors and other stakeholders
• Ensure compliance with applicable regulations and guidelines
• Provide guidance and support to research staff
• Maintain accurate and up-to-date records