Research Coordinator (1846)
About The Position
US Heart and Vascular is in need of a Research Coordinator to join our team in Tucson, AZ with Pima Heart and Vascular. Responsibilities: Responsible for ensuring study is compliance with local and federal laws and regulations Consents subject according to FDA requirements Recruits and screens potential study participants and performs intake assessments Creates and/or maintains all documents and records related to the study Extracts and inputs data as required into electronic systems Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress Manages the inventory of equipment and supplies related to the study and orders more as needed Attends meetings, events and seminars in order to promote the study Is a Liaison between study site, sponsors, cro, labs, ect Collects specimens (phlebotomy a plus), may process in a lab, and ship specimens (IATA familiarity a plus) Creates reports on each study, including notes on protocols, workload, data collection, and more May need to travel between work sites to meet with trail participants Requirements: 3+ years previous experience working in a clinical research setting Excellent written and verbal communication skills Ability to speak a second language is an asset, but not required Understanding of medical terminology as well as standard clinical procedures and protocols Prior experience training and mentoring staff members is preferred Some experience with budgets or finance Flexibility with your work schedule Strong written and verbal communication skills About Tucson, AZ: Located in Pima county, Tucson is considered the soul of the Sonoran Desert and the flavor of the Southwest, making it a hotspot for outdoor enthusiasts. Join a community rich in food, arts, culture, and the great outdoors. Tucson International Airport (TUS) offer nonstop service to 20+ destination airports, with convenient one-stop connections. Qualifications
Requirements
- 3+ years previous experience working in a clinical research setting
- Excellent written and verbal communication skills
- Understanding of medical terminology as well as standard clinical procedures and protocols
- Flexibility with your work schedule
- Strong written and verbal communication skills
Nice To Haves
- Ability to speak a second language is an asset, but not required
- Prior experience training and mentoring staff members is preferred
- Some experience with budgets or finance
Responsibilities
- Responsible for ensuring study is compliance with local and federal laws and regulations
- Consents subject according to FDA requirements
- Recruits and screens potential study participants and performs intake assessments
- Creates and/or maintains all documents and records related to the study
- Extracts and inputs data as required into electronic systems
- Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress
- Manages the inventory of equipment and supplies related to the study and orders more as needed
- Attends meetings, events and seminars in order to promote the study
- Is a Liaison between study site, sponsors, cro, labs, ect
- Collects specimens (phlebotomy a plus), may process in a lab, and ship specimens (IATA familiarity a plus)
- Creates reports on each study, including notes on protocols, workload, data collection, and more
- May need to travel between work sites to meet with trail participants
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What This Job Offers
Job Type
Full-time
Education Level
Associate degree
