Clinical Research Specialist

CommonSpirit Health • Phoenix, AZ

1d • Onsite

About The Position

The Cardiovascular (CV) Research Program has quickly grown over the past 3 years and has become a destination for novel clinical research trials. Our team members include Medical Doctors, Nurse Practitioners, Physician Assistants, Registered Research Nurses and Research Coordinators. We have received NIH grants and Sponsor funded clinical trials, all working towards improving the lives and outcomes of Cardiac Disease patients. Our Clinical Research work in Genetics, Structural Heart, Coronary Artery Disease, and Congestive Heart Failure are among the patient population disease states of which we serve. As a Research 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 Other in related field or an equivalent combination of relevant education and/ or job-related experience in lieu of degree
• Minimum 2 years related experience, upon hire

Nice To Haves

• Bachelors Other in related field
• 3+ years clinical experience, upon hire

Responsibilities

• 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: Mid Level
• Education Level: Associate degree
• Number of Employees: 5,001-10,000 employees