Research Coordinator - Clinical-Only Local Candidates

Job Description

Job Description

***Relocation assistance is NOT available for this position. Candidates must currently reside within commuting distance or be able to relocate independently as well as be prepared to begin employment within 2-4 weeks of receiving an offer***

Ironwood Cancer & Research Centers has beautiful state-of-the-art integrated Cancer and Women's Centers, with locations strategically located throughout the Valley. Each one provides a superior cancer care environment with a full spectrum of cancer related services for patients. Our multi-disciplinary team approach includes surgical oncology, medical oncology, radiation oncology, women's centers, diagnostic imaging services, integrative services including social work and nutrition, and genetic counseling.

Mission Statement : To serve the community by providing quality, comprehensive cancer care which respects the values and needs of each individual.

Overview : We are looking for a qualified and experienced Research Coordinator. Manages and coordinates all aspects of conducting clinical trials within Ironwood Physicians, PC facilities, both clinically and administrative/regulatory. Required to have in-depth knowledge of protocol requirements and ensures that studies are properly conducted in conformance with the protocol guidelines, departmental standards and good clinical practices as set forth by federal regulations and international guidelines. Schedule: Full-time, Monday through Friday day shift position and located in our Dobson location.

Essential Duties and Responsibilit ies include:

• 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.

Knowledge and Skills :

• 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.

Education and Experience :

• 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.
• We offer a competitive salary and a comprehensive benefit package including health/dental/vision and life insurance, 401K, and a caring work environment. We are an E.O.E.

Please visit our website at "Outsmarting Cancer One Patient at a Time"