Senior Clinical Research Coordinator

Job Description

Job Description

Job Location/Schedule: Monday – Friday / On-Site / Phoenix, AZ

About the Company:

We’re people with a purpose, dedicated to advancing medical innovation and healing technology through groundbreaking research, diligent patient care and strong executive management. Our hands-on management team and medical staff are committed to rapid, efficient trials that bring life-changing drugs to market faster; our research staff brings years and years of “in the trenches” experience conducting Phase 1-4 clinical studies. And each one is dedicated to curing disease and improving individual quality of life.

Mission Statement:

At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.

Summary:

Senior CRC oversees the planning and management of study projects, ensuring compliance with protocols and regulatory requirements. Coordinate the study activities, manage data collection, and support investigators with reporting and documentation. To play a critical role in maintaining the integrity and efficiency of research operations.

Essential Duties and Responsibilities:

• Provide work direction to clinical staff and back-office team
• Provide operational leadership to resolve complex study and site-level issues impacting enrollment, compliance, and timelines
• Review, comprehend and communicate study protocols
• Oversee SIV, PSV and IMV
• Assist CRC team as needed to facilitate research and business needs
• Conduct and manage clinical trials in accordance with the study protocol guidelines and internal SOP’s.
• Oversee data quality and ensure accuracy and timelines of study data across assigned protocols
• Work closely with CRO/CRA and IRB
• Manage required study start up documentation, training and timelines on assigned study protocols
• Effectively communicate with Sponsors, ensuring customer satisfaction
• Direct study resource planning and ensure appropriate allocation of supplies and equipment
• Other job duties as apparent or assigned

Qualification Requirements:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required.

Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

Education and Experience:

• Associates degree and/or completion of accredited healthcare certification program
• Ability to effectively lead, coach and direct employees
• Strong leadership skills that empower an engaged and effective team
• Exceptional communication skills, including verbal and written communication
• Ability to prioritize critical tasks and effectively manage time
• 2+ years of experience in clinical research
• 2+ years of experience working as a Clinical Research Coordinator preferred
• Comprehensive knowledge of FDA, GCP & confidentiality.
• Exceptional attention to detail and strong organizational skills
• Proven ability to multi-task in a rapidly changing environment
• High emotional intelligence, with the ability to identify and effectively control stressful situations

Benefits: Medical, Dental, Vision, 401k, PTO and more