Clinical Research Administrator Jobs in Vermont , Employment

Are you looking for an exciting opportunity to join a dynamic team in a fast-paced clinical research environment? We are looking for a Clinical Research Administrator to join our team and help us make a difference in the lives of patients. You will be responsible for managing the day-to-day operations of clinical research studies, ensuring compliance with applicable regulations, and providing administrative support to the research team. If you have a passion for clinical research and are looking for a rewarding career, this is the job for you!

Overview A Clinical Research Administrator is responsible for the management and coordination of clinical research projects. This includes overseeing the development, implementation, and evaluation of clinical research protocols, as well as the management of personnel and resources. The Clinical Research Administrator is also responsible for ensuring compliance with applicable regulations and guidelines. Detailed Job Description The Clinical Research Administrator is responsible for the overall management and coordination of clinical research projects. This includes the development, implementation, and evaluation of clinical research protocols, as well as the management of personnel and resources. The Clinical Research Administrator is also responsible for ensuring compliance with applicable regulations and guidelines. The Clinical Research Administrator will work closely with the Principal Investigator and other research staff to ensure that all research activities are conducted in accordance with established protocols and procedures. The Clinical Research Administrator will also be responsible for the preparation and submission of reports, as well as the maintenance of records and documentation. Job Skills Required

• Knowledge of clinical research protocols and procedures

• Knowledge of applicable regulations and guidelines

• Excellent organizational and communication skills

• Ability to work independently and as part of a team

• Ability to manage multiple projects and prioritize tasks

• Ability to work under pressure and meet deadlines

• Strong problem-solving and decision-making skills

• Proficiency in Microsoft Office Suite

Job Qualifications

• Bachelor’s degree in a related field

• At least two years of experience in clinical research

• Certification in clinical research (e.g. CCRA, CCRP, etc.)

Job Knowledge

• Knowledge of clinical research protocols and procedures

• Knowledge of applicable regulations and guidelines

• Knowledge of data management and analysis

• Knowledge of medical terminology

Job Experience

• At least two years of experience in clinical research

• Experience in project management

• Experience in data management and analysis

• Experience in preparing and submitting reports

Job Responsibilities

• Develop, implement, and evaluate clinical research protocols

• Manage personnel and resources

• Ensure compliance with applicable regulations and guidelines

• Prepare and submit reports

• Maintain records and documentation

• Monitor progress of research projects

• Analyze data and interpret results

• Provide guidance and support to research staff