Experienced Clinical Research Coordinator Jobs in Kentucky , Employment

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

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