Clinical Research Coordinator I-Full Time (Days)

INOVA Sports Medicine department is seeking a Clinical Research Coordinator to join the team! Our research interests include return to sport following ACL reconstruction and clinical outcomes after arthroscopy surgery. If you are interested in guiding regulatory compliance, managing research finances, supporting personnel, and engaging in other aspects of a thriving clinical research program in Sports Medicine, then we would like to hear from you by submitting your application!

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: 2023 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.