Site Director
Miami, FL | On-site
Full-Time
Not sure what skills you will need for this opportunity Simply read the full description below to get a complete picture of candidate requirements.
Lead Clinical Research Operations and Drive Study Success
Excellent opportunity for experienced clinical research leaders with expertise in Phase I and early-phase clinical trials
Are you passionate about clinical operations, site leadership, and advancing innovative therapies ? We're looking for a Site Director to lead clinical research operations at one of ERG's premier research sites, overseeing study execution, business performance, quality, regulatory compliance, and team leadership.
If you thrive in a fast-paced clinical research environment and enjoy leading high-performing teams while driving operational excellence, this could be your next opportunity.
What You'll Do
Lead the overall operations, profitability, and strategic execution of a clinical research site
Manage, mentor, and develop site staff while overseeing recruitment, onboarding, training, and performance management
Drive study enrollment, patient recruitment, retention efforts, and site performance metrics
Oversee clinical trial operations to ensure studies are conducted in compliance with protocols, GCP, ICH, HIPAA, and regulatory requirements
Partner with sponsors, investigators, business development teams, and operational leadership to evaluate and execute new research opportunities
Manage site quality assurance programs, regulatory submissions, IRB interactions, and staff training initiatives
Coordinate cross-functional teams and centralized support services to ensure successful study delivery
Serve as the primary leadership contact for sponsors, internal stakeholders, and executive management
What We're Looking For
Bachelor's degree in a scientific or healthcare-related field
7-10 years of experience in clinical operations, including 5+ years in a senior leadership role
Phase I or early-phase clinical research experience
Bilingual in English and Spanish
Knowledge and experience with:
- Clinical Research Operations
- Clinical Trial Management
- Phase I Clinical Trials
- Patient Recruitment and Retention
- GCP Compliance
- ICH Guidelines
- HIPAA Requirements
- Regulatory Affairs
- IRB Processes
- Quality Assurance
- Medical Terminology
- Team Leadership
- Business Development Support
- Site Operations
- Study Start-Up and Execution
- Microsoft Office Suite
Compensation
Base Salary: $175,000 - $200,000 annually , depending on experience and qualifications. xhqgsiq
Additional compensation and benefits package available
Sign-On Bonus Available
Relocation Assistance Available
Please Note
On-site in Miami, FL
Full-time leadership position overseeing clinical research operations
Phase I and early-phase clinical research experience required
Bilingual English/Spanish required
Overnight business travel may be required
Relocation assistance is available for qualified candidates
If this sounds like you, or someone in your network, I'd love to connect!
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This position is listed as full time and onsite.