The Clinical Research Coordinator I implement research studies and ensures research and human subject protection within Inova from site selection to study closure.
Coordinates financial aspects of study implementation and management from protocol feasibility through study closure. Develops a basic level of understanding of study coordination and the ability to perform a variety of tasks under direct supervision.
Participates in several different types of clinical studies (investigational products, study phases, therapeutic areas and indications).
Inova Employee Benefits and Perks :
- Health, Vision, and Dental Coverage
- Life Insurance, Short / Long Term Disability
- NEW ! 4 weeks PAID PARENTAL LEAVE
- Retirement : Inova matches dollar for dollar the first 5% of your eligible pay that you contribute to the plan
- Competitive salary : Pay based experience.
- Amazing Paid Time Off : Accrue PTO hours on your very first day of work.
- Supplemental Plans : Including Auto / Home Insurance discounts, Pet Insurance, Identity Theft Protection
- Additional Benefits : Educational Assistance of up to $5,250 / year, Student Loan Refinancing, Adoption Assistance, Child Care Centers, Scholarship Program, Free Parking, Exclusive savings opportunities to in-store events, theme parks, discounts, movie tickets and local offerings and so much more!
Shift : Days
Hours : Location :
Location :
Requirements for consideration :
Minimum Education :
Associate degree (or relevant experience in lieu of degree)
Years of Experience :
Two years patient care experience or 1-year clinical research experience with a bachelor's degree
Job Responsibilities
- Identifies and explains key protocol elements and performs study tasks under direct supervision.
- Explains basic elements of subject safety including the reasoning behind the required use of an Institutional Review Board / Independent Ethics Committee, study activity documentation, and event reporting requirements.
- Demonstrates subject protection under direct supervision.
- Explains the investigational products development process and identify key regulations to control these processes.
- Explains and performs study operational activities in compliance with Good Clinical Practice (GCP), and non-GCP related study management activities.
- Explains how to document data according to ALCOA-C (Attributable, Legible, Contemporaneous, Original, Accurate and Complete) principles.
- Other duties as assigned.
Utilizing random candidate selection methodology
LI-AL1
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