Clinical Research Coordinator I/II/III

Job Summary

Required Qualifications

• •Proof of legal authority to work in the United States
• •Bachelor's degree plus three (3) years of general research experience, or High School diploma/GED plus seven (7) years of general research experience
• •Obtain CRS Certification within 2 years of hire
• •Obtain CRS Certification within 2 years of hire
• •Obtain CRS Certification within 2 years of hire
• •CCRP, CCRC, or equivalent professional certification
• •Demonstrated proficiency in study planning/development
• •Demonstrated proficiency in study coordination/management
• •Demonstrated proficiency in data collection
• •Working knowledge of the Code of Federal Regulations
• •Working knowledge of the Code of Conduct for human research
• •Ability to organize complex projects
• •Attention to detail
• •Effective communication skills
• •Ability to travel
• •Ability to drive
• •Ability to walk
• •Ability to lift
• •Ability to reach
• •Ability to stoop
• •Ability to crouch
• •Ability to grasp
• •Ability to sit
• •Ability to stand
• •Ability to talk
• •Ability to hear
• •Finger dexterity
• •Ability to type/keyboard
• •Ability to schedule and appointment reminder calls
• •Ability to manage records
• •Ability to generate reports
• •Ability to manage day-to-day operations of research projects
• •Ability to maintain and manage study files
• •Ability to maintain and manage research databases
• •Ability to follow standard operating procedures
• •Ability to foster relationships with patients, study participants, family members, study personnel, site leads, collaborators, local patient and family advisory committee and regional coordinators
• •Ability to collaborate with faith-based organizations, community organizations, and other community leaders and agencies
• •Ability to participate and contribute to routine staff and organizational meetings
• •Ability to perform other duties as assigned
• •Ability to ensure quality control
• •Ability to enter data consistently and accurately
• •Ability to create and manage study files (electronic and hard files)
• •Ability to develop and maintain study timelines
• •Ability to provide recommendations for quality improvement
• •Ability to conduct enrollment and obtain consent
• •Ability to organize and conduct data collection events (collection of surveys and biometrics)
• •Ability to deliver and/or transport study-related items
• •Ability to screen potentially eligible participants
• •Ability to coordinate data collection appointments for study visits with participants
• •Ability to prepare data collection packets
• •Ability to administer survey instruments
• •Ability to collect biometrics
• •Ability to manage the day-to-day operations of the research projects
• •Ability to manage participant recruitment
• •Ability to manage consent
• •Ability to manage data collection
• •Ability to manage records
• •Ability to generate reports
• •Ability to manage study files
• •Ability to maintain research databases
• •Ability to apply knowledge of local policies, federal regulations, and guidelines
• •Ability to ensure effective and efficient workflow
• •Ability to adhere to quality standards
• •Ability to maintain a working knowledge of the Code of Federal Regulations
• •Ability to adhere to strict regulatory requirements
• •Ability to maintain and manage project/research databases within established quality control and security protocols
• •Ability to ensure study-related supplies are ordered
• •Ability to conduct data collection events
• •Ability to ensure adherence to quality standards for staff/program, and self
• •Ability to maintain and manage study files and research databases within established quality control and security protocols
• •Ability to enter data consistently and accurately
• •Ability to create and manage study files (electronic and hard files)
• •Ability to develop and maintain study timelines
• •Ability to follow standard operating procedures
• •Ability to foster relationships with patients, study participants and family members, study personnel, site leads, collaborators, local patient and family advisory committee and regional coordinators
• •Ability to collaborate with faith-based organizations, community organizations, and other community leaders and agencies
• •Ability to participate and contribute to routine staff and organizational meetings
• •Ability to perform other duties as assigned
• •Ability to maintain a working knowledge of the Code of Federal Regulations and the code of conduct for human research
• •Ability to adhere to strict regulatory requirements
• •Ability to ensure effective and efficient workflow
• •Ability to adhere to quality standards
• •Ability to maintain and manage project/research databases within established quality control and security protocols
• •Ability to enter data consistently and accurately
• •Ability to ensure quality control
• •Ability to create and manage study files (electronic and hard files)
• •Ability to generate reports
• •Ability to develop and maintain study timelines
• •Ability to follow standard operating procedures
• •Ability to provide recommendations for quality improvement
• •Ability to foster relationships with patients, study participants and family members, study personnel, site leads, collaborators, local patient and family advisory committee and regional coordinators
• •Ability to collaborate with faith-based organizations, community organizations, and other community leaders and agencies
• •Ability to participate and contribute to routine staff and organizational meetings
• •Ability to perform other duties as assigned
• •Ability to maintain a working knowledge of the Code of Federal Regulations and the code of conduct for human research
• •Ability to adhere to strict regulatory requirements
• •Ability to ensure effective and efficient workflow
• •Ability to adhere to quality standards
• •Ability to maintain and manage project/research databases within established quality control and security protocols
• •Ability to enter data consistently and accurately
• •Ability to ensure quality control
• •Ability to create and manage study files (electronic and hard files)
• •Ability to generate reports
• •Ability to develop and maintain study timelines
• •Ability to follow standard operating procedures
• •Ability to provide recommendations for quality improvement
• •Ability to foster relationships with patients, study participants and family members, study personnel, site leads, collaborators, local patient and family advisory committee and regional coordinators
• •Ability to collaborate with faith-based organizations, community organizations, and other community leaders and agencies
• •Ability to participate and contribute to routine staff and organizational meetings
• •Ability to perform other duties as assigned
• •Ability to maintain a working knowledge of the Code of Federal Regulations and the code of conduct for human research
• •Ability to adhere to strict regulatory requirements
• •Ability to ensure effective and efficient workflow
• •Ability to adhere to quality standards
• •Ability to maintain and manage project/research databases within established quality control and security protocols
• •Ability to enter data consistently and accurately
• •Ability to ensure quality control
• •Ability to create and manage study files (electronic and hard files)
• •Ability to generate reports
• •Ability to develop and maintain study timelines
• •Ability to follow standard operating procedures
• •Ability to provide recommendations for quality improvement
• •Ability to foster relationships with patients, study participants and family members, study personnel, site leads, collaborators, local patient and family advisory committee and regional coordinators
• •Ability to collaborate with faith-based organizations, community organizations, and other community leaders and agencies
• •Ability to participate and contribute to routine staff and organizational meetings
• •Ability to perform other duties as assigned
• •Ability to maintain a working knowledge of the Code of Federal Regulations and the code of conduct for human research
• •Ability to adhere to strict regulatory requirements
• •Ability to ensure effective and efficient workflow
• •Ability to adhere to quality standards
• •Ability to maintain and manage project/research databases within established quality control and security protocols
• •Ability to enter data consistently and accurately
• •Ability to ensure quality control
• •Ability to create and manage study files (electronic and hard files)
• •Ability to generate reports
• •Ability to develop and maintain study timelines
• •Ability to follow standard operating procedures
• •Ability to provide recommendations for quality improvement
• •Ability to foster relationships with patients, study participants and family members, study personnel, site leads, collaborators, local patient and family advisory committee and regional coordinators
• •Ability to collaborate with faith-based organizations, community organizations, and other community leaders and agencies
• •Ability to participate and contribute to routine staff and organizational meetings
• •Ability to perform other duties as assigned
• •Ability to maintain a working knowledge of the Code of Federal Regulations and the code of conduct for human research
• •Ability to adhere to strict regulatory requirements
• •Ability to ensure effective and efficient workflow
• •Ability to adhere to quality standards
• •Ability to maintain and manage project/research databases within established quality control and security protocols
• •Ability to enter data consistently and accurately
• •Ability to ensure quality control
• •Ability to create and manage study files (electronic and hard files)
• •Ability to generate reports
• •Ability to develop and maintain study timelines
• •Ability to follow standard operating procedures
• •Ability to provide recommendations for quality improvement
• •Ability to foster relationships with patients, study participants and family members, study personnel, site leads, collaborators, local patient and family advisory committee and regional coordinators
• •Ability to collaborate with faith-based organizations, community organizations, and other community leaders and agencies
• •Ability to participate and contribute to routine staff and organizational meetings
• •Ability to perform other duties as assigned
• •Ability to maintain a working knowledge of the Code of Federal Regulations and the code of conduct for human research
• •Ability to adhere to strict regulatory requirements
• •Ability to ensure effective and efficient workflow
• •Ability to adhere to quality standards
• •Ability to maintain and manage project/research databases within established quality control and security protocols
• •Ability to enter data consistently and accurately
• •Ability to ensure quality control
• •Ability to create and manage study files (electronic and hard files)
• •Ability to generate reports
• •Ability to develop and maintain study timelines
• •Ability to follow standard operating procedures
• •Ability to provide recommendations for quality improvement
• •Ability to foster relationships with patients, study participants and family members, study personnel, site leads, collaborators, local patient and family advisory committee and regional coordinators
• •Ability to collaborate with faith-based organizations, community organizations, and other community leaders and agencies
• •Ability to participate and contribute to routine staff and organizational meetings
• •Ability to perform other duties as assigned
• •Ability to maintain a working knowledge of the Code of Federal Regulations and the code of conduct for human research
• •Ability to adhere to strict regulatory requirements
• •Ability to ensure effective and efficient workflow
• •Ability to adhere to quality standards
• •Ability to maintain and manage project/research databases within established quality control and security protocols
• •Ability to enter data consistently and accurately
• •Ability to ensure quality control
• •Ability to create and manage study files (electronic and hard files)
• •Ability to generate reports
• •Ability to develop and maintain study timelines
• •Ability to follow standard operating procedures
• •Ability to provide recommendations for quality improvement
• •Ability to foster relationships with patients, study participants and family members, study personnel, site leads, collaborators, local patient and family advisory committee and regional coordinators
• •Ability to collaborate with faith-based organizations, community organizations, and other community leaders and agencies
• •Ability to participate and contribute to routine staff and organizational meetings
• •Ability to perform other duties as assigned
• •Ability to maintain a working knowledge of the Code of Federal Regulations and the code of conduct for human research
• •Ability to adhere to strict regulatory requirements
• •Ability to ensure effective and efficient workflow
• •Ability to adhere to quality standards
• •Ability to maintain and manage project/research databases within established quality control and security protocols
• •Ability to enter data consistently and accurately
• •Ability to ensure quality control
• •Ability to create and manage study files (electronic and hard files)
• •Ability to generate reports
• •Ability to develop and maintain study timelines
• •Ability to follow standard operating procedures
• •Ability to provide recommendations for quality improvement
• •Ability to foster relationships with patients, study participants and family members, study personnel, site leads, collaborators, local patient and family advisory committee and regional coordinators
• •Ability to collaborate with faith-based organizations, community organizations, and other community leaders and agencies
• •Ability to participate and contribute to routine staff and organizational meetings
• •Ability to perform other duties as assigned
• •Ability to maintain a working knowledge of the Code of Federal Regulations and the code of conduct for human research
• •Ability to adhere to strict regulatory requirements
• •Ability to ensure effective and efficient workflow
• •Ability to adhere to quality standards
• •Ability to maintain and manage project/research databases within established quality control and security protocols
• •Ability to enter data consistently and accurately
• •Ability to ensure quality control
• •Ability to create and manage study files (electronic and hard files)
• •Ability to generate reports
• •Ability to develop and maintain study timelines
• •Ability to follow standard operating procedures
• •Ability to provide recommendations for quality improvement
• •Ability to foster relationships with patients, study participants and family members, study personnel, site leads, collaborators, local patient and family advisory committee and regional coordinators
• •Ability to collaborate with faith-based organizations, community organizations, and other community leaders and agencies
• •Ability to participate and contribute to routine staff and organizational meetings
• •Ability to perform other duties as assigned
• •Ability to maintain a working knowledge of the Code of Federal Regulations and the code of conduct for human research
• •Ability to adhere to strict regulatory requirements
• •Ability to ensure effective and efficient workflow
• •Ability to adhere to quality standards
• •Ability to maintain and manage project/research databases within established quality control and security protocols
• •Ability to enter data consistently and accurately
• •Ability to ensure quality control
• •Ability to create and manage study files (electronic and hard files)
• •Ability to generate reports
• •Ability to develop and maintain study timelines
• •Ability to follow standard operating procedures
• •Ability to provide recommendations for quality improvement
• •Ability to foster relationships with patients, study participants and family members, study personnel, site leads, collaborators, local patient and family advisory committee and regional coordinators
• •Ability to collaborate with faith-based organizations, community organizations, and other community leaders and agencies
• •Ability to participate and contribute to routine staff and organizational meetings
• •Ability to perform other duties as assigned
• •Ability to maintain a working knowledge of the Code of Federal Regulations and the code of conduct for human research
• •Ability to adhere to strict regulatory requirements
• •Ability to ensure effective and efficient workflow
• •Ability to adhere to quality standards
• •Ability to maintain and manage project/research databases within established quality control and security protocols
• •Ability to enter data consistently and accurately
• •Ability to ensure quality control
• •Ability to create and manage study files (electronic and hard files)
• •Ability to generate reports
• •Ability to develop and maintain study timelines
• •Ability to follow standard operating procedures
• •Ability to provide recommendations for quality improvement
• •Ability to foster relationships with patients, study participants and family members, study personnel, site leads, collaborators, local patient and family advisory committee and regional coordinators
• •Ability to collaborate with faith-based organizations, community organizations, and other community leaders and agencies
• •Ability to participate and contribute to routine staff and organizational meetings
• •Ability to perform other duties as assigned
• •Ability to maintain a working knowledge of the Code of Federal Regulations and the code of conduct for human research
• •Ability to adhere to strict regulatory requirements
• •Ability to ensure effective and efficient workflow
• •Ability to adhere to quality standards
• •Ability to maintain and manage project/research databases within established quality control and security protocols
• •Ability to enter data consistently and accurately
• •Ability to ensure quality control
• •Ability to create and manage study files (electronic and hard files)
• •Ability to generate reports
• •Ability to develop and maintain study timelines
• •Ability to follow standard operating procedures
• •Ability to provide recommendations for quality improvement
• •Ability to foster relationships with patients, study participants and family members, study personnel, site leads, collaborators, local patient and family advisory committee and regional coordinators
• •Ability to collaborate with faith-based organizations, community organizations, and other community leaders and agencies
• •Ability to participate and contribute to routine staff and organizational meetings
• •Ability to perform other duties as assigned
• •Ability to maintain a working knowledge of the Code of Federal Regulations and the code of conduct for human research
• •Ability to adhere to strict regulatory requirements
• •Ability to ensure effective and efficient workflow
• •Ability to adhere to quality standards
• •Ability to maintain and manage project/research databases within established quality control and security protocols
• •Ability to enter data consistently and accurately
• •Ability to ensure quality control
• •Ability to create and manage study files (electronic and hard files)
• •Ability to generate reports
• •Ability to develop and maintain study timelines
• •Ability to follow standard operating procedures
• •Ability to provide recommendations for quality improvement
• •Ability to foster relationships with patients, study participants and family members, study personnel, site leads, collaborators, local patient and family advisory committee and regional coordinators
• •Ability to collaborate with faith-based organizations, community organizations, and other community leaders and agencies
• •Ability to participate and contribute to routine staff and organizational meetings
• •Ability to perform other duties as assigned
• •Ability to maintain a working knowledge of the Code of Federal Regulations and the code of conduct for human research
• •Ability to adhere to strict regulatory requirements
• •Ability to ensure effective and efficient workflow
• •Ability to adhere to quality standards
• •Ability to maintain and manage project/research databases within established quality control and security protocols