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Experienced Clinical Research Coordinator Jobs in Iowa

Clinical Research Coordinator Jobs
By Northwell Health At , Lake Success, 11020 $58,540 - $92,650 a year
Bachelor's Degree required, or equivalent combination of education and related experience.
Collects labels, logs, processes, and ships biological specimens for analysis according to protocol and training requirements.
1-3 years of relevant experience, required.
Responsible for coordination of a designated study or group of studies.
In research projects, oversees recruitment of subjects, implementation of study procedures, and the collection and processing of data.
Keeps accurate and up-to-date records.
Clinical Research Coordinator Ii
By Sutter Health At , Palo Alto $40.85 - $61.28 an hour
Mentors and fosters a constructive teaching environment that helps students and new teammates build confidence in their skills, knowledge and abilities.
Performs information management functions, including maintaining databases, entering and auditing data, may perform trending.
Ensures compliance with protocol guidelines and requirements of regulatory agencies.
2 years experience conducting clinical research.
2 years experience ensuring compliance with research regulations.
Equivalent experience will be accepted in lieu of the required degree or diploma.
Clinical Research Coordinator 1 Jobs
By Baylor Scott & White Health At , Dallas, 75246
Implements various protocols for assigned research projects with appropriate departments throughout the organization by interacting with PIs, clinical managers and supervisors.
Obtains knowledge of departmental functions through reading literature, attending workshops, seminars and conferences and participating in professional organizations.
Research certification or other certifications per specialty area preferred.
Proven written and oral communication skills.
Exceptional computer skills, including Microsoft Office.
Ability to manage time reactive projects in order to meet deadlines.
Clinical Research Coordinator Jobs
By Banner Health At , Gilbert, 85234
This position will support clinical trials for solid tumor patients
This position is Monday - Friday 8am-5pm, No weekends, no holidays!
Our organization supports a drug-free work environment.
Clinical Research Coordinator Jobs
By Medix™ At Cincinnati Metropolitan Area, United States
Coordinates patient care in compliance with protocol requirements
Disburses investigational drug and provide patient teaching regarding administration and other patient educational needs
Screens potential patients for protocol eligibility
Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on clinical trials
Responsible for review of consents to ensure proper execution of the informed consent process for study subjects
Oversees the preparation of orders by physicians to assure that protocol compliance is maintained
Clinical Research Coordinator Jobs
By Valley Medical Center At , Renton, Wa $63,857 - $96,426 a year
Must have a working knowledge and be skilled in the use of personal computers, information storage and retrieval systems.
Coordinate with Health Information Management to assure appropriate identification of research protocol participants in the electronic health record.
Management of all miscellaneous tasks involved with coordinating clinical trials
Four year degree preferred, national certification a plus.
Minimum 1 year of experience in a clinical research environment.
Performs other related job duties as required.
Clinical Research Coordinator Jobs
By University of California, Davis At , Davis, 95616, Ca $30.03 - $48.29 an hour
Project management and organizational skills for coordinating aspects of research studies.
Data management experience. Ability to design and maintain an efficient filing and record keeping system.
Knowledge and experience with industry sponsored research.
CITI Certification for Biomedical Researchers and Good Clinical Practice (GCP) Certification after date of hire
Several years of Clinical Research Coordinator experience, with demonstrated increasing level of responsibility is preferred
Experience working with older adult population with cognitive impairment.

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