Research Coordinator - Clinical-Only Local Candidates-Glendale

Ironwood Physicians, P.C.; Glendale (AZ); On-site; USD 52,000 - 76,000; Full time

Job summary

Ironwood Cancer & Research Centers in Glendale seeks a Research Coordinator to manage clinical trials, ensuring protocol compliance and efficient study conduct.

You will coordinate with investigators, monitor subject safety, collect data, and support regulatory files, with Monday–Friday day shift.

Qualifications

• Associate or Bachelor’s Degree required.
• Clinical experience in Oncology or acute care.
• Prior research and phlebotomy experience.
• IATA, human subjects protection training or GCP training highly desirable.
• We offer a competitive salary and comprehensive benefits.

Responsibilities

• Acts as liaison between investigators, other study staff, primary care providers, IRB and sponsor.
• Reviews studies for clinical and operational feasibility with Investigator and Director of Research.
• Screens, consents, enrolls and follows study subjects ensuring protocol compliance.
• Responsible for data and source documentation, adverse experience reporting, and regulatory files maintenance.
• Develops screening/enrollment/follow up mechanisms.
• Ensures randomization and blinding procedures per protocol guidelines.
• Schedules and performs patient procedures, assessments, and testing as required by the protocol.

Skills

Excellent clinical skills

Organized and detail oriented

MS Office proficiency

Office equipment operation

Education

Associate or Bachelor’s Degree

Clinical oncology experience

Phlebotomy experience

GCP/IATA training desirable

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Research Coordinator - Clinical-Only Local Candidates-Glendale

Full-time Regular Glendale, AZ, US

4 days ago Requisition ID: 8281

***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 Glendale location.

Essential Duties and Responsibilities 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.
• 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.