Senior Clinical Research Coordinator — Oncology Trials

University of Alabama at Birmingham; Birmingham (AL); Vor Ort; USD 61.000 - 99.000; Vollzeit

Zusammenfassung

University of Alabama at Birmingham is seeking a Clinical Research Coordinator III to lead interventional trial coordination and support senior team members. The role covers study lifecycle management, protocol adherence, consent, data collection, and regulatory compliance.

Strong candidates will have a related degree with at least five years of experience, and may hold CCRP/CCRC certification. OnCore and oncology trial experience are advantageous. This is an onsite position at UAB.

Qualifikationen

• Bachelor's degree in a related field and five (5) years of related experience required.
• CCRC or CCRP certification preferred.
• Work experience may NOT substitute for education requirement.
• Preferred: clinical research experience.
• Ability to lead others in coordinating oncology clinical trials.
• Knowledge of clinical research regulatory/compliance affairs.
• Strong problem-solving and analytical skills.
• Excellent written and verbal communication skills.
• Good organizational and prioritization abilities.
• Ability to walk at least one mile daily and lift 5–10 pounds.

Aufgaben

• Serve as lead coordinator, overseeing less experienced staff to ensure quality and regulatory compliance in clinical research operations.
• Coordinate and manage the research study lifecycle from start-up through close-out.
• Coordinate and conduct screening, scheduling, consent, data collection, and documentation per GCP.

Kenntnisse

Clinical research experience

Leadership abilities

Regulatory/compliance knowledge

GCP knowledge

Communication skills

Ausbildung

Bachelor's degree in a related field

Five years of related experience

Tools

OnCore

Jobbeschreibung

University of Alabama at Birmingham is seeking a Clinical Research Coordinator III to lead interventional trial coordination and support senior team members. The role covers study lifecycle management, protocol adherence, consent, data collection, and regulatory compliance.

Strong candidates will have a related degree with at least five years of experience, and may hold CCRP/CCRC certification. OnCore and oncology trial experience are advantageous. This is an onsite position at UAB.