Oncology Clinical Research Coordinator - 256289

Medix™; Murrieta (CA); Presencial; USD 72 000 - 90 000; Tempo integral

Resumo da oferta

Medix is seeking an Oncology Clinical Research Coordinator in Murrietta, CA to coordinate protocol-driven visits and ensure regulatory compliance. The role emphasizes safety, informed consent, and accurate data capture across study visits in oncology trials.

The position requires 2+ years in clinical research coordination, with a preference for Phase I oncology trial exposure and strong knowledge of GCP/ICH guidelines and HIPAA.

Qualificações

• 2+ years of experience as a Clinical Research Coordinator.
• Phase I oncology trial experience preferred.

Responsabilidades

• Coordinate and conduct protocol-required study visits and procedures for oncology clinical trials, with preference for Phase I experience.

Conhecimentos

Oncology experience

Clinical Research Coordinator

GCP/ICH knowledge

Formação académica

Bachelor’s degree preferred

Ferramentas

Microsoft Office / Office365

Descrição da oferta de emprego

Oncology Clinical Research Coordinator (Murietta, CA)

Format: Direct Hire

Hours: Full time, Monday - Friday, 8am-5/6pm

Pay: $72,000 - $90,000

Responsibilities:

• Coordinate and conduct protocol-required study visits and procedures for oncology clinical trials, with preference for experience supporting Phase I studies.
• Obtain and document informed consent in accordance with federal regulations, GCP, and IRB requirements.
• Accurately document patient assessments, observations, test results, and other study-related activities in source documents and CRFs/eCRFs.
• Schedule and manage participant visits while ensuring adherence to protocol timelines and sponsor requirements.
• Recruit and screen eligible participants to meet study enrollment goals while maintaining ethical and regulatory compliance.
• Monitor and report adverse events (AEs) and serious adverse events (SAEs) in accordance with sponsor and regulatory timelines.
• Maintain accurate records and accountability for study materials, investigational products, and lab supplies.
• Ensure compliance with GCP, ICH guidelines, HIPAA regulations, and site SOPs.
• Communicate regularly with investigators, study team members, sponsors, and other stakeholders to ensure smooth study operations.
• Participate in investigator meetings, trainings, and continuing education to remain current on clinical research regulations and best practices.
• Represent the organization professionally when interacting with patients, sponsors, IRBs, and clinical partners.
• Perform additional study-related duties as assigned.

Qualifications:

• Bachelor’s degree preferred but not required.
• 2+ years of experience as a Clinical Research Coordinator, with oncology experience strongly preferred.
• Phase I oncology clinical trial experience preferred.
• Strong knowledge of clinical research regulations, GCP, and protocol compliance.

Preferred Skills:

• Strong organizational and multitasking abilities in a fast-paced research environment.
• Excellent written and verbal communication skills.
• Proficiency with Microsoft Office / Office365 and clinical research documentation systems.
• Ability to collaborate effectively with cross-functional teams and manage competing priorities.
• Strong attention to detail, problem-solving, and process improvement skills.