JOB ID: 2888221

Position: Clinical Research Coordinator

Shift Schedule: Day 5x8-Hour (08:00 - 17:00)

Location: Los Angeles, CA 90025

Start date; 07/07/2025

Job Types: 13 weeks Contract

Pay: $35 - $40 per hour

Years of Experience:

3 year(s)

Note: REQUIRED: Must have 2 year of relevant exp in one of the Research Specialties marked as preferred above AND 1 year of Oncology experience

Position Summary:

We are seeking a highly motivated and detail-oriented Clinical Research Coordinator (CRC) with at least one year of oncology experience to join our research team. The CRC will play a pivotal role in managing and coordinating clinical trials focused on oncology, ensuring strict compliance with protocol, regulatory requirements, and Good Clinical Practice (GCP).

Required:

• Associates Degree

• 3+ years of experience as CRC

• 2 years of RECENT (within 1-2 years) experience in Oncology

• BLS

• Longevity in previous roles

• Interest in temp to perm

Preferred

• Bachelors Degree

• SoCRA or ACRP Certification

• Phlebotomy Certified

• Medical Assistant Diploma

Primary Duties and Responsibilities

• Establishes and executes logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety.

• Coordinates administrative functions of research studies, including scheduling of patients for research visits, procedures and labs and completion and maintenance of consent forms, case report forms, SAE’s and source documents.

• Responsible for screening and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and supporting the informed consent process.

• Responsible for accurate and timely data collection, documentation, entry and reporting, including resolution of queries from sponsors or regulatory entities.

• Coordinates institutional, pharmaceutical and internal audits, including facilitating third party study monitoring and designs and implements needed corrective actions.

• Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.

• Responsible for timely submission of adverse events, serious adverse events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.

• Identifies quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality.

• Plans and coordinates strategies for increasing research participant enrollment, and/or improving clinical research efficiency as needed.

• Provides technical support for the preparation of grant proposals, publications, presentations and special projects.

• Provides assistance with research project budget development, including identifying and classifying routine care vs. research related care and provides assistance with research participant research billing and reconciliation.

• Attend meetings and conferences related to research activities, including research staff meetings.

• Participate in planning, workshops, evaluation meetings, and seminars, educational or administrative meetings as necessary or requested; Participates in training and education of new research personnel.

Precision Scans is an equal-opportunity employer, committed to cultural diversity. Precision Scans will provide equal consideration for employment to all qualified applicants without regard to their race, religion, ancestry, national origin, sex, sexual orientation, age, disability, marital status, domestic partner status, or medical condition.