Clinical Research Coordinator, RN - Flexible/Remote

START Center for Cancer Research; Los Angeles (CA); On-site; USD 62,000 - 90,000; Full time

Benefits offered by this job

Health coverage

401(k) plan

Life insurance

Disability insurance

Health savings account

Paid time off

Flexible schedule

Remote work options

Job summary

The START Center for Cancer Research seeks a Clinical Research Coordinator, RN to support daily activities of early phase oncology trials. You will ensure protocol compliance, consent, data accuracy, and patient safety under supervision of senior staff.

Responsibilities include coordinating multiple protocols, training staff, screening patients, and preparing source documents in a fast-paced setting at the Los Angeles site. Strong GCP knowledge and communication skills are essential.

Qualifications

• Associate’s degree in Nursing.
• RN license in state practicing.
• 2 years of clinical research experience.
• Basic understanding of oncology clinical trials, particularly Phase 1 studies.
• Strong attention to detail and accuracy in data collection and documentation.
• Ability to manage multiple tasks and meet deadlines in a fast-paced environment.
• Excellent organizational and time-management skills.
• Strong communication skills, both written and verbal.
• Proficient in Microsoft Office Suite and clinical trial management software.
• Working knowledge of GCP and regulatory requirements.

Responsibilities

• Communicate on a regular basis with Study Sponsor’s, CRO’s, staff, etc. regarding questions, concerns, as well as status of the protocol.
• Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study.
• Create/review forms created or revised for assigned trials to assure protocol compliance.
• Maintain files using standardized study document labeling and filing procedures.
• Implement initial protocol and amendments, training staff who will be involved in patient treatment and management.
• Maintain an up-to-date contact list.
• Assist with patient screening and determination of eligibility.
• Facilitate the informed consent process ensuring that consent is appropriately completed.
• Prepare and manage source documents according to standard operating procedures.
• Recognize deviations to the protocol and will work with leadership and staff to address corrective actions to prevent deviations.
• Assist data coordinator team with case report form completion and query resolution.
• Work with the Principal Investigator to complete and submit Serious Adverse Event reports.
• Perform protocol specific closeout related activities in conjunction with the data coordinator.
• Provide documentation for all deviations whether related to the protocol or a SOP.
• Ensure that all team members involved understand and adhere to assigned protocols.
• Perform telephone triage assessments of patients on trial when necessary.
• Provide patient education regarding participation in a clinical trial, chemotherapy/biotherapy/investigational agent administration and potential side effects.

Skills

Attention to detail

Multitasking

Organizational skills

Communication skills

Time management

Interpersonal skills

GCP knowledge

Education

Associate’s degree in Nursing

RN license

Bachelor’s degree in Nursing

Tools

Microsoft Office Suite

Clinical trial management software

Job description

The START Center for Cancer Research seeks a Clinical Research Coordinator, RN to support daily activities of early phase oncology trials. You will ensure protocol compliance, consent, data accuracy, and patient safety under supervision of senior staff.

Responsibilities include coordinating multiple protocols, training staff, screening patients, and preparing source documents in a fast-paced setting at the Los Angeles site. Strong GCP knowledge and communication skills are essential.