Clinical Research Specialist II

Benefits

Qualifications

• •This role is designed to be 100% onsite, giving you the opportunity to collaborate closely with your team and immerse yourself in the energy of our workplace
• •Bachelor's Degree required
• •5 years of experience in area of research specialty required

Responsibilities

• •The Clinical Research Specialist II provides clinical research expertise by participating in the design and implementation of research projects as needed
• •Responsible for specific and assigned aspects of research infrastructure development, coordinates projects, and communicates status and improvement areas to leadership
• •May implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts
• •Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB)
• •Provides research writing activities such as developing scientific documents for abstracts, publications, presentations, funding applications, and study protocols
• •Serves as an internal advisor for specific departmental activities
• •Provides guidance regarding project planning, project logistics, and project implementation
• •Provides clinical research expertise by participating in the design and implementation of research projects as needed by the department or institution
• •Responsible for specific and assigned aspects of research infrastructure development and/or maintenance
• •Coordinates research projects at an institutional or departmental level
• •Communicates project status and improvement areas with leadership in a timely manner
• •Projects may include, but are not limited to investigator-initiated protocol development including protocol writing, case report form development, budget development, and coordination of departmental research committees
• •May implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts
• •Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board
• •Maintains research practices using Good Clinical Practice (GCP) guidelines
• •Maintains strict patient confidentiality according to HIPAA regulations and applicable law
• •Participates in required training and education programs
• •Shift Duration : 8 hour
• •15 more items(s)