On-Site Clinical Research Coordinator – Mobile, AL

Forefront Dermatology; Mobile (AL); On-site; USD 65,000 - 90,000; Full time

Job summary

Forefront Dermatology in Mobile, Alabama seeks a Clinical Research Coordinator to drive strategy and execution across assigned studies, ensuring regulatory compliance and delivering enrollment and data-quality outcomes. You will engage directly with participants and exercise independent judgment in identifying risks that affect study success.

This 100% on-site position requires coordinating protocol-specific deliverables, managing sponsor/CRO interactions, and mentoring the research team to

Qualifications

• Advanced knowledge of clinical research regulations, quality management principles, and documentation standards.
• Ability to interpret and apply requirements to maintain compliance and audit readiness.
• Independently manage multiple studies with prioritized, performance-driven execution.
• Strong communication and interpersonal skills with sponsors, CROs, investigators, and teams.

Responsibilities

• Direct clinical research operations across protocols, establishing workflows and deliverables.
• Oversee regulatory compliance, safety reporting, and audit readiness activities.
• Lead enrollment strategies, optimize screening, and meet performance targets.
• Manage external partnerships with sponsors, investigators, and CROs.
• Mentor research staff and promote protocol adherence across sites.
• Assess new opportunities, plan feasibility, and guide protocol development.

Skills

Clinical Research

Regulatory Compliance

Data Quality

Enrollment Strategy

Stakeholder Engagement

Education

Bachelor's Degree

Job description

Forefront Dermatology in Mobile, Alabama seeks a Clinical Research Coordinator to drive strategy and execution across assigned studies, ensuring regulatory compliance and delivering enrollment and data-quality outcomes. You will engage directly with participants and exercise independent judgment in identifying risks that affect study success.

This 100% on-site position requires coordinating protocol-specific deliverables, managing sponsor/CRO interactions, and mentoring the research team to