Research Regulatory Specialist

CommonSpirit Health • Phoenix, AZ

3d • Onsite

About The Position

The Ivy Brain Tumor Center at Barrow Neurological Institute is a non-conventional non-profit program offering state-of-the-art clinical trials for patients with the most aggressive form of brain cancer. It is home to the largest collection of Phase 0 trials for brain tumors in the world. Our multidisciplinary team of brain tumor specialists and scientists are accelerating drug discovery and precision medicine in neuro-oncology to identify the most promising first-in-class therapies for brain tumor patients. As a Research Regulatory Specialist, you will lead and manage complex clinical research, collaborating with Principal Investigators to ensure protocol adherence and scientific integrity. You will actively contribute to study design and methodology to advance research objectives. Every day you will oversee data collection, management, and quality control, ensuring accuracy and regulatory compliance. You will analyze data, prepare detailed reports, and contribute to presentations and publications. To be successful in this role, you will possess advanced knowledge of research methodologies and regulatory guidelines, demonstrating exceptional problem-solving and critical thinking skills. Your ability to manage multiple projects, mentor junior staff, and communicate complex scientific information effectively is essential.

Requirements

• Associates degree in related field or an equivalent combination of relevant education and / or job-related experience in lieu of degree
• Minimum (2) years related experience

Nice To Haves

• Bachelors degree in related field
• Three (3+) years clinical experience

Responsibilities

• Coordinates and participates in clinical research studies.
• Collects, compiles, documents, and reports clinical research data.
• Prepares project reports as it relates to program management and grant funding.
• Coordinates and schedules subject study visits to ensure adequate supplies, procedures and investigator availability.
• Provides study specific, individualized education to study subjects and families.
• Ensures all appropriate subject consents are obtained.
• Collects and processes protocol required specimens.
• Acts as a liaison between Sponsor, Investigator, and Study Subject
• Collects all required study data and completes CRFs in a timely, accurate manner.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree