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Experienced Clinical Research Coordinator Jobs in Indiana

Clinical Research Coordinator Jobs
By Advarra At Indianapolis, IN, United States
Perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study protocol.
Performs duties and responsibilities in a highly organized manner.
Maintain up-to-date working knowledge of regulatory compliance guidelines as defined by the federal regulations, IRBs, and state laws.
3 years of gene therapy or CNS experience required.
CCRP/CCRC/SOCRA certifications or equivalent preferred
Current training in human subjects protection education, Good Clinical Practice, and HIPAA Privacy
Clinical Research Coordinator Jobs
By AION Biosystems At Albany, New York Metropolitan Area, United States
●Proficient in Microsoft Office including Word, Excel, Project and PowerPoint, Data management platforms, EMR systems
A combination of education and experience may be considered
●Ensure remote patient monitoring platforms are integrated between the hospital system and Idion
●Maintain completeness of site documents and manage patient and study data
●Ability to prioritize assignments, manage time efficiently and assist in project oversight to meet established deadlines
●Attention to detail with outstanding organizational skills
Clinical Research Coordinator Jobs
By University of Louisville At Center, IN, United States
Maintain in-depth knowledge of protocol requirements and complete all required training prior to performing tasks.
Collect, document, and analyze data obtained from research studies.
Screen patients for entry into clinical studies and assess patients at each visit regarding compliance with protocol, complications, and difficulties.

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