The US Oncology Network · 9 hours ago
Clinical Research Coord.
Teaneck, NJ
Full-time
Onsite
Entry, Mid Level
$49K/yr - $70K/yr
2+ years expThe US Oncology Network is seeking a Clinical Research Coordinator who will report to the Manager of Clinical Research. This role is responsible for coordinating and conducting assigned research studies, including patient recruitment, data collection, and compliance with clinical protocols.
CommunitiesHealth CareMedicalOncologyTest and Measurement
Responsibilities
Leads recruitment efforts and screens potential patients for eligibility for studies
Ability to achieve enrollment targets on assigned studies
Obtains informed consent from patients and conducts study visits for clinical trials
Creates Case Report Forms
Completes assessments on study subjects as per protocol
Documents study assessments
Enters study data into EDC systems
Collects, processes, stores and ships lab specimens; documents lab procedures, lab results and follows up with patients and medical staff as necessary
Coordinates, monitors visits with CRAs for each trial to ensure accurate documentation; makes corrections to data as necessary
Assists during sponsor and FDA audits
Responsible for submissions and reports to the IRB; maintains documentation of IRB communications and decisions
Documents adverse events and notifies PI, sponsor and IRB
Assumes test article accountability
Possesses a sound and in-depth understanding of each protocol that has been assigned as a primary responsibility
Maintains compliance with Good Clinical Practice; Clinical Safety Data Management, 21 CFR, and has IATA certification
Travels to investigator meetings
Participates in weekly meetings with the research team, provides study metrics
Responds to requests in a timely manner, gives/receives correct information, encourages dialogue and follow-through, secures accurate signatures, maintains files in an organized and up-to-date manner
Other tasks as required
Qualification
Required
Bachelor's degree preferably in Science or related field
Equivalent relevant experience and/or training in lieu of education is acceptable
2+ years' relevant experience (e.g. research, clinical, interaction with study population, program coordination)
Experience with research studies, recruitment and retention of subjects and procedures associated with the studies
Ability to achieve enrollment targets on assigned studies
Obtains informed consent from patients and conducts study visits for clinical trials
Creates Case Report Forms
Completes assessments on study subjects as per protocol
Documents study assessments
Enters study data into EDC systems
Collects, processes, stores and ships lab specimens; documents lab procedures, lab results and follows up with patients and medical staff as necessary
Coordinates, monitors visits with CRAs for each trial to ensure accurate documentation; makes corrections to data as necessary
Assists during sponsor and FDA audits
Responsible for submissions and reports to the IRB; maintains documentation of IRB communications and decisions
Documents adverse events and notifies PI, sponsor and IRB
Assumes test article accountability
Possesses a sound and in-depth understanding of each protocol that has been assigned as a primary responsibility
Maintains compliance with Good Clinical Practice; Clinical Safety Data Management, 21 CFR, and has IATA certification
Travels to investigator meetings
Participates in weekly meetings with the research team, provides study metrics
Responds to requests in a timely manner, gives/receives correct information, encourages dialogue and follow-through, secures accurate signatures, maintains files in an organized and up-to-date manner
Company
The US Oncology Network
Every day, The US Oncology Network helps approximately 3,300 providers deliver value-based, integrated care for patients—close to home.
10001+ employees
Funding
Current Stage
Late StageTotal Funding
unknown2010-12-30Acquired
Leadership Team
R. Steve Paulson
National Policy Board Executive Committee
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