Our Clinical Research Coordinator job description includes the responsibilities, duties, skills, education, qualifications, and experience.
About the Clinical Research Coordinator role
A Clinical Research Coordinator is responsible for organizing and managing clinical trials and research studies. This involves recruiting and coordinating with research participants, administering surveys and tests, collecting and organizing data, and ensuring compliance with ethical and regulatory standards. They must also be knowledgeable of medical terminology and have excellent communication and organizational skills.
Role Purpose
The purpose of a Clinical Research Coordinator (CRC) is to oversee and coordinate the administrative, clinical, and data-related activities of clinical research studies. This includes overseeing the development and implementation of protocols, coordinating activities among the research team and other stakeholders, monitoring regulatory compliance, and managing data collection, entry, and analysis. CRCs are responsible for ensuring the accuracy and completeness of the research data and for maintaining the confidentiality of the research data according to institutional policies and procedures. Additionally, CRCs are often responsible for educating research staff and participants about the research process and providing guidance to research staff on the proper implementation of the research protocol.
Clinical Research Coordinator Summary
The Clinical Research Coordinator is responsible for overseeing and managing the day-to-day operations of clinical research studies. This includes managing research budgets, coordinating study teams, ensuring compliance with protocol, and monitoring patient safety. The Clinical Research Coordinator will also be responsible for developing and implementing recruitment and retention plans, reviewing and submitting data, and maintaining accurate and complete study records. Additionally, the Clinical Research Coordinator may be responsible for assisting in the development of study protocols, participating in monitoring visits, and preparing reports for data analyses. The Clinical Research Coordinator must have excellent communication and organizational skills, the ability to work independently, and the ability to interact effectively with study sponsors, investigators, and other study teams.
Clinical Research Coordinator Duties
- Plan and coordinate all activities related to the clinical research process
- Recruit and screen participants for clinical research studies
- Collect, manage and analyze data from clinical research studies
- Organize and maintain clinical research records
- Ensure accurate and timely completion of clinical research studies
- Monitor adherence to protocols and research regulations
- Prepare and submit reports to sponsors
- Provide guidance and support to clinical research personnel
Clinical Research Coordinator Skills
- Strong organizational and communication skills
- Experience in clinical research or related field
- In-depth knowledge of clinical research protocols
- Proficiency with computer software applications
- Ability to manage multiple tasks simultaneously
Clinical Research Coordinator Requirements
- Bachelor's degree in a related field
- Experience in clinical research
- Knowledge of FDA regulations and ethical standards
- Ability to manage multiple projects and prioritize tasks
Personal Traits
- organizational skills
- attention to detail
- collaborative attitude
- good communication