Clinical Research Associate I - Microbiome Program at City of Hope Duarte, CA

Itlearn360; Duarte (CA); On-site; USD 55,000 - 80,000; Full time

Job summary

A leading company in innovative medical research seeks a Clinical Research Associate I to manage research protocols and ensure compliance with regulatory standards. The role requires strong interpersonal skills and attention to patient confidentiality, alongside the ability to work independently in a dynamic environment.

Qualifications

• One year of experience in a healthcare setting, preferably in research.
• Adaptability, independence, professional demeanor.

Responsibilities

• Conduct protocol management for research protocols.
• Maintain regulatory documents and protocol compliance.
• Recruit patients for studies.

Skills

Patient confidentiality

Interpersonal skills

Adaptability

Independence

Education

Associate's Degree

Bachelor's Degree

Job description

Clinical Research Associate I - Microbiome Program job at City of Hope. Duarte, CA.

Join the forefront of groundbreaking research at the Beckman 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.

Come join us as a Clinical Research Associate I. If you are adaptable, independent, and professional in diverse settings, then this is the right fit for you! As a successful candidate, you will:

• Conduct protocol management for an assigned set of multiple research protocols.
• Maintain current and accurate protocol documentation; notify investigators of pertinent protocol changes.
• Maintain and complete regulatory documents for IRB, DSMB, and PRMC/CPRMC.
• Compile and submit data on appropriate forms according to protocol requirements.
• Establish and maintain interpersonal relationships with patients, visitors, and other hospital personnel, while assuring confidentiality of patient information.
• Collect and deliver specimens for analysis, using appropriate or specified equipment for collecting and handling specimens; ensure proper labeling and obtain pertinent clinical and protocol information on request forms; develop and maintain knowledge of various aspects of processing specimens, paying particular attention to safety practices.
• Work with physician or nurse to see that protocol related tests and evaluations are ordered per protocol guidelines.
• Play active role in recruitment of patients to study.
• Perform protocol specific duties as required per the research study.

Your qualifications should include:

• Associate's Degree.
• Experience may substitute for minimum education requirements.
• One-year experience working in a health care setting, preferably in research.

Preferred qualifications:

• Bachelor's Degree.
• Medical Record, Health Information Systems, clinical trials exposure or related health field.

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 commitment to diversity, equity, and inclusion, please click here . To learn more about our Comprehensive Benefits, please CLICK HERE .