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Full-time

Cancer Clinical Research Coordinator 2 - Neurology (Hybrid)

Competitive

Stanford, CAScience & PharmaceuticalPosted 19d ago

You'll complete your application on the employer's website.

Role overview

Job description

Cancer Clinical Research Coordinator 2 - Neurology (Hybrid) jobs in United States

Tags

25 applicants

Original Job Post

Stanford University School of Medicine

Cancer Clinical Research Coordinator 2 - Neurology (Hybrid)

82

GOOD MATCH

Experience Level

100

Skill

68

Industry Exp.

76

Responsibilities

Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials

Oversee data management for research projects. Develop and manage systems to organize, collect, report, and monitor data collection. Extract, analyze, and interpret data

Develop project schedules, targets, measurements, and accountabilities, as assigned. Lead team meetings and prepare/approve minutes

Formally supervise, train, and/or mentor new staff or students, as assigned, potentially including hiring, preparing or assisting with the preparation of performance evaluations, and performing related duties, in addition to instruction on project work

Audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions and respond to requests and questions

Collaborate with principal investigators and study sponsors, monitor and report serious adverse events, and resolve study queries

Provide leadership in determining, recommending, and implementing improvements to policies/processes; define best practices

Develop study budget with staff and principal investigator, identifying standard of care versus study procedures. Track patient and study specific milestones, and invoice sponsors according to study contract

Ensure regulatory compliance. Regularly inspect study documents to ensure ongoing regulatory compliance

Work with principal investigator to ensure Investigational New Drug applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are completed

Preferred

Experience working with oncology clinical research studies

Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred

Benefits

Hybrid work arrangement

Glassdoor

4.0

Stanford Medicine improves health through leadership, diversity and collaborative discoveries and innovation in health care, education and research.

Stanford, California, USA

https://med.stanford.edu/scgpm.html

Late Stage

Leadership Team

Laila Soudi

Co-Founder, Co-Director MENA Health Program

Monica Hanson

Co-Founder and Director, (ACT), CCARE, Research Center at Stanford School of Medicine

Recent News

Business Wire

The Foundation for the National Institutes of Health Announces Recipients of the Deeda Blair Research Initiative for Disorders of the Brain

2026-05-20

BioSpace

NeuroDex and Stanford Researchers Publish First Evidence of CNS Target Engagement for GLP-1 and PPARγ Agonists Using Blood-Based Neuron-Derived Extracellular Vesicles

2026-04-23

News-Medical.Net

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2026-04-22

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Qualifications

Minimum of two (2) years of experience in a clinical research setting

Bachelor's degree in a related field and two years of experience in clinical research, or an equivalent combination of education and relevant experience

Strong interpersonal skills

Proficiency in Microsoft Office and database applications

Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices

Knowledge of medical terminology

Experience working with oncology clinical research studies

Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred

Minimum of two (2) years of experience in a clinical research setting.

Bachelor’s degree in a related field and two years of experience in clinical research, or an equivalent combination of education and relevant experience.

Required skills

Oncology Clinical Research, Clinical Research, Microsoft Office, HIPAA, FDA Regulations, Institutional Review Board Requirements, Clinical Practice (GCP), Medical Terminology, Clinical Research Certification SoCRA, Clinical Research Certification ACRP

Preferred skills

Experience working with oncology clinical research studies

Experience

2+ years

Interested in this role?

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