Research Assistant - Clinical

ZipRecruiter; Phoenix (AZ); On-site; USD 45,000 - 65,000; Full time

Job summary

A leading healthcare provider is seeking a qualified Research Assistant to support clinical trials in a comprehensive cancer care environment. The role involves managing regulatory compliance, quality data entry, and assisting in the education of research staff. Ideal candidates should possess strong clinical skills, attention to detail, and relevant educational background. This full-time position offers competitive salary and benefits, contributing to a caring and professional work environment.

Benefits

Health/Dental/Vision insurance

Life insurance

401K

Qualifications

• Degree required in related field (Associate or Bachelor’s).
• Training in human subjects protection or GCP desirable.

Responsibilities

• Assist in managing and conducting clinical trials.
• Maintain regulatory files and ensure compliance.
• Responsible for data quality and drug accountability.

Skills

Clinical skills

Attention to detail

Leadership skills

Communication skills

Team building

Computer skills

Education

Associate or Bachelor’s Degree

IATA, Human subjects protection training, or GCP training

Tools

Microsoft Office

Job description

Job DescriptionJob Description

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, social service support, nutritionist, integrative services, 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 Assistant to assist in managing and conducting clinical trials and ensure that studies are properly conducted in conformance with the protocol guidelines, departmental standards, and good clinical practices.

Schedule: Full-time, Monday through Friday day shift position.

Essential Duties and Responsibilities:

• Assists with maintenance of complete regulatory files, data entry, drug receipt, drug storage, and transportation and other administrative duties as assigned.
• Responsible for quality of data.
• Assists in ensuring compliance with department standards and all federal regulations and international guidelines of good clinical practice.
• Active in maintaining continued education and professional growth through participation in continuing education programs.
• Assists with lab processing and shipping.
• Assists with completion of CRFs, data entry/query resolution within protocol specified timelines.
• Assists to ensure proper study drug accountability, including receipt, storage, dispensing and transportation.
• Assist Research Nurses in the maintenance of regulatory documents.
• Assists and participates in study initiation visits, monitoring visits, closeout visits and audit visits.
• Assists with of new staff and ongoing education of other staff in the research department as appropriate

Knowledge and Skills:

• Excellent clinical and functional skills.
• Organized and detail oriented.
• Strong leadership skills.
• Strong communication and team building skills a must.
• Computer skills required (Microsoft Office).

Education and Experience:

• Associate or Bachelor’s Degree .
• 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.

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