I
Clinical Research Coordinator 1 - Oncology
Inova Health System
10 hours ago
Full-time
On-site
Fairfax, Virginia, United States
Occupational Therapist
Inova Schar Cancer Research is looking for a dedicated Clinical Research
Coordinator 1 - Oncology to join the Team. This full-time role will be day-shift
working Monday – Friday located in Fairfax, VA.
The Clinical Research Coordinator 1 - Oncology implements 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 is consistently ranked a national healthcare leader in safety, quality and
patient experience. We are also proud to be consistently recognized as a top
employer in both the D.C. metro area and the nation.
Featured Benefits:
* Committed to Team Member Health: offering medical, dental and vision
coverage, and a robust team member wellness program.
* Retirement: Inova matches the first 5% of eligible contributions – starting
on your first day.
* Tuition and Student Loan Assistance: offering up to $5,250 per year in
education assistance and up to $10,000 for student loans.
* Mental Health Support: offering all Inova team members, their
spouses/partners, and their children 25 mental health coaching or therapy
sessions, per person, per year, at no cost.
* Work/Life Balance: offering paid time off, paid parental leave, flexible work
schedules.
Clinical Research Coordinator 1 - Oncology 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.
* Explains the importance of professional conduct and describe leadership
principles that impact the effective operation of an investigative site.
* Explains the variety of communication channels, roles and relationship and
outlets for study results that impact the conduct of clinical research.
* May perform other duties as assigned.
Minimum Qualifications:
* Education: Associate’s Degree or relevant experience in lieu of a degree
* Experience: 2 years of patient care experience or 1 year of clinical research
experience with a Bachelor’s Degree
Preferred Qualifications:
* Certified Clinical Research Coordinator preferred.
* Experience leading informed consent discussions and enrolling participants in
clinical research studies preferred.
* Experience developing, implementing, and/or evaluating clinical research
protocols and operational workflows preferred.
* Experience screening patients for research study eligibility and
collaborating effectively within multidisciplinary teams, including
physicians, healthcare providers, research coordinators, and other research
staff preferred.
* Experience collecting, managing, and verifying research data for accuracy
against source documentation preferred.
We are Inova, Northern Virginia’s leading nonprofit healthcare provider. Every
day, our 26,000+ 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 is an Equal Opportunity 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.
Coordinator 1 - Oncology to join the Team. This full-time role will be day-shift
working Monday – Friday located in Fairfax, VA.
The Clinical Research Coordinator 1 - Oncology implements 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 is consistently ranked a national healthcare leader in safety, quality and
patient experience. We are also proud to be consistently recognized as a top
employer in both the D.C. metro area and the nation.
Featured Benefits:
* Committed to Team Member Health: offering medical, dental and vision
coverage, and a robust team member wellness program.
* Retirement: Inova matches the first 5% of eligible contributions – starting
on your first day.
* Tuition and Student Loan Assistance: offering up to $5,250 per year in
education assistance and up to $10,000 for student loans.
* Mental Health Support: offering all Inova team members, their
spouses/partners, and their children 25 mental health coaching or therapy
sessions, per person, per year, at no cost.
* Work/Life Balance: offering paid time off, paid parental leave, flexible work
schedules.
Clinical Research Coordinator 1 - Oncology 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.
* Explains the importance of professional conduct and describe leadership
principles that impact the effective operation of an investigative site.
* Explains the variety of communication channels, roles and relationship and
outlets for study results that impact the conduct of clinical research.
* May perform other duties as assigned.
Minimum Qualifications:
* Education: Associate’s Degree or relevant experience in lieu of a degree
* Experience: 2 years of patient care experience or 1 year of clinical research
experience with a Bachelor’s Degree
Preferred Qualifications:
* Certified Clinical Research Coordinator preferred.
* Experience leading informed consent discussions and enrolling participants in
clinical research studies preferred.
* Experience developing, implementing, and/or evaluating clinical research
protocols and operational workflows preferred.
* Experience screening patients for research study eligibility and
collaborating effectively within multidisciplinary teams, including
physicians, healthcare providers, research coordinators, and other research
staff preferred.
* Experience collecting, managing, and verifying research data for accuracy
against source documentation preferred.
We are Inova, Northern Virginia’s leading nonprofit healthcare provider. Every
day, our 26,000+ 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 is an Equal Opportunity 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.