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Overview Clinical Research Associate I (CRA I) is a professional who works in the clinical research industry and is responsible for the management of clinical trials. The CRA I is responsible for the day-to-day management of the clinical trial, including the coordination of all activities related to the trial, such as patient recruitment, data collection, and reporting. Detailed Job Description The Clinical Research Associate I is responsible for the day-to-day management of clinical trials. This includes the coordination of all activities related to the trial, such as patient recruitment, data collection, and reporting. The CRA I is also responsible for ensuring that all clinical trial activities are conducted in accordance with applicable regulations and guidelines. The CRA I will also be responsible for the preparation of clinical trial documents, such as protocols, case report forms, and informed consent forms. The CRA I will also be responsible for the monitoring of clinical trial sites to ensure that all activities are conducted in accordance with the protocol and applicable regulations and guidelines. Job Skills Required

• Knowledge of clinical research regulations and guidelines

• Excellent organizational and communication skills

• Ability to work independently and as part of a team

• Ability to manage multiple tasks and prioritize work

• Ability to work in a fast-paced environment

• Ability to work with minimal supervision

• Proficiency in Microsoft Office Suite

Job Qualifications

• Bachelor’s degree in a related field

• At least one year of experience in clinical research

• Certification in Good Clinical Practice (GCP)

• Knowledge of clinical research regulations and guidelines

Job Knowledge

• Knowledge of clinical research regulations and guidelines

• Knowledge of clinical trial design and methodology

• Knowledge of clinical trial data management

• Knowledge of clinical trial monitoring

• Knowledge of clinical trial reporting

Job Experience

• At least one year of experience in clinical research

• Experience in clinical trial design and methodology

• Experience in clinical trial data management

• Experience in clinical trial monitoring

• Experience in clinical trial reporting

Job Responsibilities

• Coordinate all activities related to the clinical trial

• Prepare clinical trial documents, such as protocols, case report forms, and informed consent forms

• Monitor clinical trial sites to ensure that all activities are conducted in accordance with the protocol and applicable regulations and guidelines

• Ensure that all clinical trial activities are conducted in accordance with applicable regulations and guidelines

• Prepare and submit clinical