Clinical Research Coordinator

Benefits

Qualifications

• •Facilitates data quality and integrity
• •Obtain and maintain appropriate credentialing approval from the
• •Healthcare related training with current licensure/certification in
• •their field OR Bachelor's degree from an accredited university with
• •a major in the area of research being conducted
• •Certified Clinical Research Professional as defined by The Society
• •of Clinical Research Associates or Certified Clinical Research
• •Professionals OR Ability to obtain certification as a Clinical
• •Research Professional/Coordinator within two years from date of
• •hire or upon eligibility
• •Air Force Specialty Code
• •universities participating in federal financial aid programs to
• •Nationally recognized as a Great College to Work For ,
• •Ready to start building a rewarding career in a positive
• •positive culture that puts people first
• •12 more items(s)

Responsibilities

• •clinic conduct, marketing, and data management of all clinical
• •research activities in assigned department(s)
• •Carries out
• •supervisory responsibilities in accordance with policies and
• •Responsibilities may include training new
• •employees; assisting with planning, assigning, and directing work;
• •addressing complaints and resolving problems
• •frequently exposed to fumes or airborne particles
• •occasionally exposed to toxic or caustic chemicals and dangerous
• •bodily fluids
• •Approximately 5-15% travel (often long-distance) is
• •Develop and maintain relationships with faculty members
• •interested in or currently conducting clinical research
• •Develop and maintain relationships with assigned
• •pharmaceutical, medical device, and other medical manufacturers
• •Actively market the Clinical Research Institute
• •Facilitate IRB application and submission via Cayuse
• •Facilitate ongoing and timely communication with the IRB via
• •Cayuse system
• •Recruit and enroll human subjects while protecting subjects and
• •Maintain study files/documents on all assigned studies
• •Facilitates data quality and integrity
• •Assist with development and management of research study
• •Assist faculty/staff with development of research
• •Assist with clinical research education and training of
• •volunteers, students, new employees
• •Attend affiliated clinical research meetings and professional
• •meetings where research and compliance training may occur
• •Obtain SoCRA (CCRP) or ACRP (CCRC) certification when
• •M-F 8am - 5pm and occasional late evenings or weekends
• •Coordinator as defined by the Association of Clinical Research
• •maintain and disclose campus crime statistics and security
• •By October 1 of each year, institutions must publish
• •and distribute their Annual Campus Security Policy & Crime
• •Statistics Report (ASR) to current and prospective students and
• •and advancing knowledge through innovative research
• •33 more items(s)