Experienced Clinical Research Coordinator for Genetic Studies of Alzheimer's Disease and Related Dementias - Remote Opportunity with Travel Requirements
Introduction to the University of Miami and the Hussman Institute
The University of Miami, a prestigious institution renowned for its academic excellence and innovative research, is seeking a highly motivated and experienced Clinical Research Coordinator to join its team. The Hussman Institute for Human Genomics, a leading research center within the university, is dedicated to advancing our understanding of human genetics and its applications in medicine. As a key member of this team, you will play a vital role in contributing to the success of our genetic studies of Alzheimer's disease and related dementias.
Job Overview
We are looking for an experienced Clinical Research Coordinator to assist in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. The successful candidate will work closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols. This role will involve traveling throughout the United States to enroll participants in our genetic studies, collecting biological samples, and coordinating study activities and personnel.
Key Responsibilities
Assist in participant recruitment and retention activities, including screening potential study participants for eligibility
Perform study procedures, routine tests, data collection/recording, and daily operations of moderate risk clinical research protocols
Collect, process, pack, and ship specimens according to protocol, applicable standards, and regulations
Maintain study binders and filings according to protocol requirements, UM, and department policy
Distribute study drug materials according to practice standards and clinical credentials as delegated by the Principal Investigator
Monitor, document, report, and follow-up on study unanticipated/adverse events and protocol deviations
Assist in implementing protocol amendments under direct supervision of the Principal Investigator
Assist with study orientation and protocol-related in-services to research team and clinical staff
Monitor protocol implementation and study progress; keep investigators fully apprised of study progress; submit progress reports according to established schedule
Learn the research team and assist with communications/interactions with sponsor, data coordinating centers, compliance monitors, collaborators, investigators' academic administrative personnel, and departments
Assist in administrative tasks of study personnel, including orientation, documenting core competencies, certification mandates, safety/responsible conduct of research education, and performance reviews
Essential Qualifications
Bachelor's degree in a relevant field required
Minimum 2 years of relevant experience in clinical research coordination
Strong knowledge of clinical research principles, practices, and regulations
Excellent communication, organizational, and interpersonal skills
Ability to work independently and as part of a team
Proficiency in Microsoft Office and electronic data capture systems
Preferred Qualifications
Experience working with genetic studies, Alzheimer's disease, or related dementias
Spanish language proficiency
Certification in clinical research coordination (e.g., CCRC, CCRP)
Experience with data management and analysis software
Skills and Competencies
Strong attention to detail and ability to maintain accurate records
Excellent problem-solving and critical thinking skills
Ability to work in a fast-paced environment and prioritize multiple tasks
Strong analytical and technical skills
Ability to maintain confidentiality and handle sensitive information
Career Growth Opportunities and Learning Benefits
As a Clinical Research Coordinator at the University of Miami, you will have the opportunity to work with a talented team of researchers and clinicians, contributing to the advancement of genetic research and its applications in medicine. You will also have access to professional development opportunities, including training and education in clinical research principles, practices, and regulations. Our institution is committed to fostering a culture of excellence, innovation, and collaboration, providing a supportive environment for career growth and advancement.
Work Environment and Company Culture
The University of Miami is an equal opportunity employer, committed to diversity, equity, and inclusion. We offer a dynamic and supportive work environment, with a strong focus on teamwork, collaboration, and open communication. Our institution values work-life balance, providing a comprehensive benefits package, including medical, dental, tuition remission, and more. As a member of our team, you will be part of a vibrant community of scholars, researchers, and clinicians, working together to advance knowledge and improve human health.
Compensation, Perks, and Benefits
We offer a competitive salary and a comprehensive benefits package, including medical, dental, tuition remission, and more. As a full-time employee, you will be eligible for a range of perks and benefits, including paid time off, holidays, and retirement plans. Our institution is committed to recognizing and rewarding the contributions of our employees, providing opportunities for professional growth and development.
Conclusion
If you are a motivated and experienced clinical research professional looking for a challenging and rewarding opportunity, we encourage you to apply for this exciting role. As a Clinical Research Coordinator at the University of Miami, you will be part of a talented team of researchers and clinicians, contributing to the advancement of genetic research and its applications in medicine. Don't miss this opportunity to join our team and make a meaningful difference in the lives of others. Apply now and take the first step towards a rewarding and challenging career in clinical research coordination.
Apply Now
The University of Miami, a prestigious institution renowned for its academic excellence and innovative research, is seeking a highly motivated and experienced Clinical Research Coordinator to join its team. The Hussman Institute for Human Genomics, a leading research center within the university, is dedicated to advancing our understanding of human genetics and its applications in medicine. As a key member of this team, you will play a vital role in contributing to the success of our genetic studies of Alzheimer's disease and related dementias.
Job Overview
We are looking for an experienced Clinical Research Coordinator to assist in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. The successful candidate will work closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols. This role will involve traveling throughout the United States to enroll participants in our genetic studies, collecting biological samples, and coordinating study activities and personnel.
Key Responsibilities
Assist in participant recruitment and retention activities, including screening potential study participants for eligibility
Perform study procedures, routine tests, data collection/recording, and daily operations of moderate risk clinical research protocols
Collect, process, pack, and ship specimens according to protocol, applicable standards, and regulations
Maintain study binders and filings according to protocol requirements, UM, and department policy
Distribute study drug materials according to practice standards and clinical credentials as delegated by the Principal Investigator
Monitor, document, report, and follow-up on study unanticipated/adverse events and protocol deviations
Assist in implementing protocol amendments under direct supervision of the Principal Investigator
Assist with study orientation and protocol-related in-services to research team and clinical staff
Monitor protocol implementation and study progress; keep investigators fully apprised of study progress; submit progress reports according to established schedule
Learn the research team and assist with communications/interactions with sponsor, data coordinating centers, compliance monitors, collaborators, investigators' academic administrative personnel, and departments
Assist in administrative tasks of study personnel, including orientation, documenting core competencies, certification mandates, safety/responsible conduct of research education, and performance reviews
Essential Qualifications
Bachelor's degree in a relevant field required
Minimum 2 years of relevant experience in clinical research coordination
Strong knowledge of clinical research principles, practices, and regulations
Excellent communication, organizational, and interpersonal skills
Ability to work independently and as part of a team
Proficiency in Microsoft Office and electronic data capture systems
Preferred Qualifications
Experience working with genetic studies, Alzheimer's disease, or related dementias
Spanish language proficiency
Certification in clinical research coordination (e.g., CCRC, CCRP)
Experience with data management and analysis software
Skills and Competencies
Strong attention to detail and ability to maintain accurate records
Excellent problem-solving and critical thinking skills
Ability to work in a fast-paced environment and prioritize multiple tasks
Strong analytical and technical skills
Ability to maintain confidentiality and handle sensitive information
Career Growth Opportunities and Learning Benefits
As a Clinical Research Coordinator at the University of Miami, you will have the opportunity to work with a talented team of researchers and clinicians, contributing to the advancement of genetic research and its applications in medicine. You will also have access to professional development opportunities, including training and education in clinical research principles, practices, and regulations. Our institution is committed to fostering a culture of excellence, innovation, and collaboration, providing a supportive environment for career growth and advancement.
Work Environment and Company Culture
The University of Miami is an equal opportunity employer, committed to diversity, equity, and inclusion. We offer a dynamic and supportive work environment, with a strong focus on teamwork, collaboration, and open communication. Our institution values work-life balance, providing a comprehensive benefits package, including medical, dental, tuition remission, and more. As a member of our team, you will be part of a vibrant community of scholars, researchers, and clinicians, working together to advance knowledge and improve human health.
Compensation, Perks, and Benefits
We offer a competitive salary and a comprehensive benefits package, including medical, dental, tuition remission, and more. As a full-time employee, you will be eligible for a range of perks and benefits, including paid time off, holidays, and retirement plans. Our institution is committed to recognizing and rewarding the contributions of our employees, providing opportunities for professional growth and development.
Conclusion
If you are a motivated and experienced clinical research professional looking for a challenging and rewarding opportunity, we encourage you to apply for this exciting role. As a Clinical Research Coordinator at the University of Miami, you will be part of a talented team of researchers and clinicians, contributing to the advancement of genetic research and its applications in medicine. Don't miss this opportunity to join our team and make a meaningful difference in the lives of others. Apply now and take the first step towards a rewarding and challenging career in clinical research coordination.
Apply Now