Clinical Research Associate I

City of Hope; California, Duarte (MO, CA); On-site; USD 45,000 - 70,000; Full time

Job summary

An established industry player in medical research is seeking a Clinical Research Associate I to join their innovative team. In this role, you will conduct protocol management for various research studies, ensuring compliance and maintaining critical documentation. Your ability to build strong relationships with patients and staff will be key to your success as you contribute to groundbreaking research in the fight against serious illnesses. If you are adaptable and professional in diverse settings, this opportunity offers a chance to make a real difference in the healthcare field.

Qualifications

• 1+ years of experience in a healthcare setting, preferably in research.
• Associate's Degree or equivalent experience is required.

Responsibilities

• Conduct protocol management for multiple research protocols.
• Maintain accurate protocol documentation and regulatory documents.
• Establish relationships with patients and hospital personnel.

Skills

Protocol Management

Regulatory Documentation

Interpersonal Skills

Specimen Collection

Education

Associate's Degree

Bachelor's Degree (Preferred)

Job description

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.

Qualifications

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 Comprehensive Benefits, please CLICK HERE.