Clinical Study Specialist Jobs in Tennessee , Employment

Are you looking for an exciting opportunity to join a dynamic team of clinical research professionals? We are seeking a Clinical Study Specialist to join our team and help us advance our mission of improving patient care through clinical research. As a Clinical Study Specialist, you will be responsible for managing clinical studies, ensuring compliance with regulatory requirements, and providing support to clinical investigators. If you are passionate about clinical research and have the skills and experience necessary to succeed in this role, we want to hear from you!

Overview A Clinical Study Specialist is a healthcare professional who is responsible for the planning, implementation, and management of clinical studies. They work closely with clinical research teams to ensure that all aspects of the study are conducted in accordance with applicable regulations and protocols. Clinical Study Specialists are responsible for the coordination of all activities related to the study, including the recruitment of participants, data collection, and analysis. Detailed Job Description Clinical Study Specialists are responsible for the planning, implementation, and management of clinical studies. They work closely with clinical research teams to ensure that all aspects of the study are conducted in accordance with applicable regulations and protocols. Clinical Study Specialists are responsible for the coordination of all activities related to the study, including the recruitment of participants, data collection, and analysis. They are also responsible for the preparation of study documents, such as protocols, informed consent forms, and study reports. In addition, Clinical Study Specialists are responsible for the training of research staff, the monitoring of study progress, and the management of study budgets. Job Skills Required

• Knowledge of clinical research regulations and protocols

• Excellent organizational and communication skills

• Ability to work independently and as part of a team

• Ability to manage multiple tasks and prioritize effectively

• Proficiency in Microsoft Office Suite

• Knowledge of medical terminology

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)

Job Knowledge

• Knowledge of clinical research regulations and protocols

• Knowledge of medical terminology

• Knowledge of data collection and analysis methods

• Knowledge of study design and implementation

Job Experience

• At least two years of experience in clinical research

• Experience in the preparation of study documents

• Experience in the training of research staff

• Experience in the monitoring of study progress

• Experience in the management of study budgets

Job Responsibilities

• Plan, implement, and manage clinical studies

• Ensure that all aspects of the study are conducted in accordance with applicable regulations and protocols

• Coordinate all activities related to the study, including the recruitment of participants, data collection, and analysis

• Prepare study documents, such as protocols, informed consent forms, and study reports

• Train research staff

• Monitor study progress

• Manage study budgets