DPS Clinical Research Assistant I

City of Hope; Duarte (CA); On-site; USD 55,000 - 75,000; Full time

Job summary

City of Hope Beckman Research Institute in Duarte, CA is seeking a Clinical Research Assistant I to manage multiple research protocols, ensure regulatory compliance, and support data collection. This role involves participant registration, data submission, and active recruitment efforts under supervision within a dynamic research setting.

The ideal candidate has an Associate’s Degree (Bachelor’s preferred) and experience with medical records data extraction, medical terminology, and health

Qualifications

• Read, identify and extract pertinent data from medical records.
• Ability to read, write and comprehend medical terminology.
• Medical Record, Health Information Systems, or related health field.

Responsibilities

• Manage an assigned set of multiple research protocols to assure efficiency and regulatory compliance.
• Maintain current and accurate protocol documentation and notify investigators of pertinent protocol changes.
• Ensure participants are appropriately registered and maintain documentation of participant registration.
• Compile and submit data on appropriate forms according to protocol requirements.
• Ensure protocol compliance through monitoring of study requirements and schedule protocol-related activities.
• Play an active role in recruiting participants for the study.
• Assist in training and mentoring new clinical research staff members.
• Perform protocol-specific clinical duties as required by the research study.
• Perform data management and data analyses as required by the research study.

Skills

Protocol management

Data management

Participant recruitment

Training staff

Education

Associate’s 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.

Join us as a Clinical Research Assistant I in which you will manage an assigned set of multiple research protocols to assure efficiency and regulatory compliance of the protocol.

As a successful candidate, you will:

• Conduct protocol management for an assigned set of multiple research protocols.
• Maintain current and accurate protocol documentation and notify investigators of pertinent protocol changes.
• Ensure participants are appropriately registered and maintain documentation of participant registration.
• Compile and submit data on appropriate forms according to protocol requirements.
• Ensure protocol compliance through intense monitoring of specific study requirements and schedule protocol-related activities.
• Play an active role in the recruitment of participants for the study.
• Assist in training and mentoring new clinical research staff members.
• Perform protocol-specific clinical duties as required by the research study.
• Perform data management and data analyses as required by the research study.
• Establish and maintain interpersonal relationships with participants, visitors, and other hospital personnel while ensuring the confidentiality of participant information.
• Collect and deliver specimens for analysis using appropriate 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, with particular attention to safety practices.
• Identify and communicate important protocol and data management issues or problem areas to the supervisor.

Your qualifications should include:

·Associate’s Degree.Bachelor’s Degree preferred.Experience may substitute for minimum education requirements.

• Read, identify and extract pertinent data from medical records.
• Ability to read, write and comprehend medical terminology.
• Medical Record, Health Information Systems, 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, pleaseCLICK HERE.