Research Coordinator - Clinical-Only Local Candidates-Glendale

Ironwood Women's Centers; Glendale (AZ); Hybrid; USD 55,000 - 75,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401K

Job summary

Ironwood Cancer & Research Centers in Glendale, AZ is seeking a qualified Research Coordinator to manage clinical trials within Ironwood Physicians, PC facilities. The role covers clinical and administrative duties to ensure studies follow protocol guidelines and regulatory standards.

Candidates should have oncology or acute care experience, knowledge of regulatory requirements, and be able to begin within 2–4 weeks of offer, with strong organizational and data management skills.

Qualifications

• 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.

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.
• 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.

Skills

Clinical skills

Organizational skills

Microsoft Office

Attention to detail

Education

Associate degree

Bachelor's degree

Tools

GCP training

IATA training

Human subjects protection training

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

10 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 Centershas 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.

Please visit our website at www.ironwoodcrc.com. "Outsmarting Cancer One Patient at a Time"