Clinical Research Coordinator I, Pulmonary
About The Position
When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Under general supervision and direction will be responsible for the coordination and administration of multiple research studies. Works closely with principal investigators and research staff facilitating all aspects of assigned clinical trials. Implements study protocols in accordance to regulatory and institutional requirements. Sets up administrative systems to manage the progress of each study while screening, recruiting and following study participants and collecting and reporting study data. Interacts with study participants diagnosed with various medical conditions and diagnoses.
Requirements
- Bachelor’s degree required
- 0-2 years of experience in a research or medical setting
- Ability to address problems that are routine, somewhat repetitive and generally solved by following clear directions and procedures
- Ability to travel nationally to other research sites, attend investigator meetings and educational conferences as required
- Strong organizational, multi-tasking, attention to detail and communication skills
- Ability to take direction, set priorities and work somewhat independently
- Ability to demonstrate a positive attitude and respond to request in a timely and respectful manner
- Ability to work in small teams, interact with professional personnel at all levels of an organization, and work with study participants of various diseases compassionately and respectfully
- Experience with computer systems, including web-based applications
- In the absence of any of these skills, demonstrates the ability to be thoroughly trained to meet organizational standards
- Beth Israel Lahey Health requires that all staff be vaccinated against influenza (flu) as a condition of employment
Responsibilities
- Coordination and administration of multiple research studies
- Works closely with principal investigators and research staff facilitating all aspects of assigned clinical trials
- Implements study protocols in accordance to regulatory and institutional requirements
- Sets up administrative systems to manage the progress of each study while screening, recruiting and following study participants and collecting and reporting study data
- Interacts with study participants diagnosed with various medical conditions and diagnoses
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
