Clinical Research Coordinator

Responsibilities

The Clinical Research Coordinator will coordinate investigator-initiated and industry-sponsored clinical trials of targeted theranostic in patients with various types of cancer according to Good Clinical Practices (GCP), internal standard operating procedure (SOPs), and University policies and procedures such as HIPAA guidelines; Collect and maintain patient data in appropriate digital formats; Create patient profiles on CareConnect, schedule patients for search visits and procedures, and enroll/disenroll patients on OnCore.

You will also maintain detailed records and enter information into a database; Maintain a well-organized study; follow all safety and procedural regulations; Maintain and follow-up on information and referring physicians' questionnaires as appropriate. There will be patient interaction (face-to-face, phone, and email); Coordination & facilitation of monitoring and auditing visits; and management & resolution of study queries via sponsor EHRs.
Qualifications

REQUIRED:

Knowledge of basic computer skills including MS Excel, Word, etc

Ability to create weekly concise updates enumerating patient numbers, ethnicity, other demographic data etc.

Familiarity with RedCap, CareConnect and OnCore

Familiarity with Nuclear Medicine, theranostics and Oncology

Ability to organize raw data into a comprehensible form

Ability to maintain research patient charts

Ability to communicate effectively to convey results

Interpersonal skills to effectively interact with faculty, staff, postdoctoral fellows and students

UCLA is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected Veteran status.

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