Clinical Research Assistant I

City of Hope, Inc.; West Arcadia (CA); On-site; USD 40,000 - 60,000; Full time

Job summary

Join a pioneering research team at the Beckman Research Institute of City of Hope as a Clinical Research Assistant I. This role focuses on managing clinical research protocols and supporting personalized patient care related to cancer treatment. The position requires an Associates degree and offers opportunities to make a significant impact in the field.

Qualifications

• Associates degree required; Bachelor’s preferred.
• Experience with medical records and clinical trials is preferred.
• Ability to read and comprehend medical terminology.

Responsibilities

• Conduct protocol management of multiple research protocols.
• Ensure participants are registered and maintain documentation.
• Perform data management and analyses.

Skills

Data management

Clinical trials knowledge

Medical terminology

Record review

Education

Associates degree

Bachelor's degree (preferred)

Job description

Join the forefront of groundbreaking research at theBeckman Research Institute of City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.

A Clinical Research Assistant I role is available under Dr. Rusha Bhandari.She is a is a board-certified pediatric hematologist/oncologist who specializes in survivorship, which enables her to continue providing care and personalized late effects screening for patients long after they complete their cancer treatment.Dr. Bhandari’s research focuses on identifying methods to mitigate toxicities from cancer treatment, with the goal of improving long-term patient outcomes.

As a successful candidate, you will:

·Conduct protocol management of multiple research protocols.

·Maintain current and accurate protocol documentation

·Ensure participants are appropriately registered and maintain documentation of participant registration.

·Compile and submit data on appropriate forms according to protocol requirements.

·Perform protocol specific clinical duties as required per the research study.

·Perform data management and data analyses

·Collect and deliver specimens for analysis

Your qualifications should include:

·Associates degree.Experience may substitute for minimum education requirements.Bachelors preferred.

·Read, identify and extract pertinent data from medical records

·Read, write and comprehend medical terminology

·Experience with medical record review, health information systems, and/or clinical trials is preferred

City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.

City of Hope is an equal opportunity employer.

To learn more about our Comprehensive Benefits, pleaseCLICK HERE.