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Clinical Research Coordinator 1-Full Time (Days)

Inova Health System | Falls Church, VA, US, 22042

Posted 3 hours ago


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Description

INOVA's Cancer Research Team is seeking a Clinical Research Coordinator to join their team!

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!

See Full List of Benefits and Eligibility Here: 2024 INOVA BENEFITS GUIDE

Requirements for consideration:

Minimum Education:

  • Bachelor's degree in related field (or relevant experience in lieu of degree equivalent to 4 years)

Years of Experience:

  • 3 years patient care experience, including 2 years of research or 2 years healthcare experience.

Certification:

  • Basic Life Support
  • CRC Certification- must apply for certification after 2 years clinical research experience.

Job Responsibilities

  • Acts as a specialized research professional on multiple ongoing research studies.
  • Facilitates and coordinates daily clinical trial activities and plays a critical role in the conduct of the study.
  • Works collaboratively with the entire Inova study team, sponsors, and monitors to ensure productivity and timely completion of studies.
  • Participates in a broad range of different types of clinical studies and operates e-clinical technologies independently.
  • Oversees investigational product development process and applies key regulatory requirements.
  • Executes Good Clinical Practice (GCP)-related clinical study activities and non-GCP-related clinical study activities.
  • Documents data in accordance with ALCOA-C principles (Attributable, Legible, Contemporaneous, Original, Accurate and Complete).
  • Other duties as assigned.

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