Job Title: CRC

Work Location: Los Angeles County, California

Summary:

This position is responsible for independently coordinating clinical research studies, ensuring accuracy, efficiency, and compliance with regulatory requirements. The role involves close collaboration with physicians, patients, sponsors, and research teams to support all aspects of clinical trial execution.

Responsibilities:

• Identify and screen potential participants for clinical trial eligibility and facilitate the informed consent process.
• Organize and schedule research visits, procedures, and study-related activities, ensuring protocol adherence.
• Collaborate with clinical staff to document patient conditions, adverse events, medications, and protocol compliance.
• Maintain accurate source documentation and study records, and ensure timely data collection, entry, and reporting.
• Respond to sponsor queries, support monitoring and auditing activities, and track study metrics and patient accrual.
• Assist with regulatory submissions, including adverse events, protocol deviations, and safety communications.
• Participate in research team meetings, training, audits, SOP development, and quality improvement initiatives.
• Provide training to staff, identify new research opportunities, and travel to satellite clinics as required.

Qualifications:

• Bachelor’s degree (BA/BS) required.
• Certification in clinical research (ACRP, SOCRA, or equivalent).
• Minimum 1 year of clinical research coordination experience, preferably in oncology/hematology.
• Knowledge of oncology/hematology terminology and clinical research practices.
• Healthcare experience and strong knowledge of medical terminology.
• Excellent written and verbal communication skills; strong organizational skills and attention to detail.
• Ability to work independently and collaboratively with multidisciplinary teams.
• Professionalism and confidentiality in handling sensitive patient information; strong customer service skills.
• Ability to travel to satellite clinics as needed and lift up to 25 pounds.
• Strict adherence to HIPAA and applicable confidentiality laws.

Published Category: Clinical Operations & Development