Clinical Research Associate I - Medical Oncology

City of Hope

Duarte, CA

JOB DETAILS
SKILLS
Analysis Skills, Brokerage, Cancer, Clinical Information, Clinical Information Systems, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Data Analysis, Diabetes, Disease Prevention and Control, Healthcare, Interpersonal Skills, Medical Records, Medicine, Nursing, Oncology, Organizational Skills, Patient Confidentiality, Project/Program Management, Regulatory Compliance, Sample/Specimen Processing, Specimen Collection, Testing
LOCATION
Duarte, CA
POSTED
30+ days ago

Join the forefront of groundbreaking research at City of Hope where we are 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 to 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, under which you will manage an assigned set of clinical research studies and protocols to assure efficiency and regulatory compliance.

As a successful candidate, you will:

• Work on data abstraction and analysis. • Interface with existing institutional resources, including Posiedon, Honest Broker, STATA, RedCap, Excel, and others. • Download and manipulate data from external sources, including the National Cancer Database and SEER. • Provide project management for computational projects. • Assist PIs and supervisors with write-up of results and notify them of any roadblocks. • Conduct protocol management for an assigned set of clinical studies within the department. • Maintain current and accurate protocol documentation. • Notify PIs and supervisors of pertinent protocol changes and other data management issues or problem areas. • Complete and maintain regulatory documents for IRB, DSMB, and PRMCCPRMC. • Compile and submit data on appropriate forms according to protocol. • Play an active role in recruitment of patients to department studies. • Establish and maintain interpersonal relationships with patients, visitors, and other COH personnel while assuring confidentiality of patient information. • Work with PIs and nurses to schedule protocol-related tests and evaluations. • Perform other duties as outlined in the approved protocol.

Collect and deliver specimens for analysis using appropriate materials and procedures specified in the protocol. 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 and shipping instructions.

Maintain professional growth and development through seminars, workshops, and professional affiliations to maintain certification, licensure, and/or keep abreast of the latest trends in the field.

Ensure work environment is organized and functions efficiently. Attend and participate in meetings as required. Provide staff relief as required to meet the needs of the department.

Your qualifications should include:

• Associates Degree • Experience may substitute for minimum education requirements • One-year experience working in a healthcare setting, preferably in research • Preferred qualifications: • Bachelors 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.

About the Company

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City of Hope