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Ironwood Cancer and Research Centers · 2 days ago

Research Coordinator - Clinical

Mesa, AZ, US

Full-time

Onsite

New Grad, Entry Level

Ironwood Cancer & Research Centers is dedicated to providing quality cancer care and is looking for a qualified and experienced Research Coordinator. This role involves managing and coordinating all aspects of conducting clinical trials, ensuring compliance with protocol guidelines and federal regulations.

Health CareMedical

Responsibilities

Acts as liaison between investigators, other study staff, primary care providers, IRB and sponsor

Reviews studies for clinical and operational feasibility, along with the Investigator and Director of Research

Screens, consents, enrolls and follows study subjects ensuring protocol compliance and close monitoring while subjects are on study utilizing Research Nurses’ oversight for help with clinical decision making

Responsible for all data and source documentation, adverse experience reporting, and will assist Regulatory Specialist in the maintenance of complete regulatory files

Develops screening/enrollment/follow up mechanisms

Ensures that randomization procedures and blinding procedures, as applicable, are followed as per protocol guidelines

Schedules and performs patient procedures, assessments, evaluations and testing as required by the protocol, including but not limited to blood sample collection, processing and shipping, ECG, vital signs, etc., as applicable

Qualification

Clinical trial managementOncology experienceData entryPhlebotomy experienceIATA certificationGCP trainingMicrosoft Office proficiencyOrganizational skillsDetail oriented

Required

Acts as liaison between investigators, other study staff, primary care providers, IRB and sponsor

Reviews studies for clinical and operational feasibility, along with the Investigator and Director of Research

Screens, consents, enrolls and follows study subjects ensuring protocol compliance and close monitoring while subjects are on study utilizing Research Nurses' oversight for help with clinical decision making

Responsible for all data and source documentation, adverse experience reporting, and will assist Regulatory Specialist in the maintenance of complete regulatory files

Develops screening/enrollment/follow up mechanisms

Ensures that randomization procedures and blinding procedures, as applicable, are followed as per protocol guidelines

Excellent clinical and functional skills

Organized and detail oriented

Data entry experience a plus

Proficiency in Microsoft Office, Word, Outlook, and Internet

Ability to use office equipment, computer

Associate or Bachelor's Degree

Clinical experience in Oncology or other acute care

Prior research and phlebotomy experience

Current IATA, Human subjects protection training or GCP training highly desirable