Clinical Research Coordinator 1-Full Time (Days)

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: Varies

Location: INOVA Clinic And Schar Cancer

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

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We are Inova, Northern Virginia’s leading nonprofit healthcare provider. Every day, our 24,000+ team members provide world-class healthcare to the communities we serve. Our people are the reason we're a national leader in healthcare safety, quality and patient experience. And from best-in-class facilities to professional development opportunities, we support them at every step. At Inova, we're constantly striving to be ever better — to shape a more compassionate future for healthcare. 

Inova Health System is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to age, color, disability, gender identity or expression, marital status, national or ethnic origin, political affiliation, pregnancy (including childbirth, pregnancy-related conditions and lactation), race, religion, sex, sexual orientation, veteran status, genetic information, or any other characteristics protected by law.