Clinical Site Lead: Multi-Site Research & Compliance

Alcanza Clinical Research, LLC; Fredericksburg (VA); On-site; USD 75,000 - 105,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

Health Savings Account (HSA)

401(k) with safe harbor match

Job summary

Alcanza Clinical Research, LLC in Fredericksburg, VA, is seeking a Clinical Site Manager to oversee site operations, ensure protocol compliance, patient safety, and on-site visits within ICH/GCP guidelines. You will lead study teams, manage resources, track milestones, and partner with investigators to meet timelines and sponsor expectations.

Bi-lingual not required. This role requires an Associate’s degree and 3+ years in clinical research; leadership experience is preferred.

Qualifications

• Associate’s degree required with clinical research experience.
• 3+ years in clinical research; management experience preferred.
• Bi-lingual English/Spanish a plus.

Responsibilities

• Oversee site operations, ensuring protocol and GCP compliance.
• Provide on-site oversight of visits, documentation, and follow-up.
• Lead study teams, manage resources, and monitor milestones.
• Collaborate with investigators to meet timelines and sponsor goals.
• Manage staff performance, training, and regulatory adherence.
• Escalate risks and implement corrective actions when needed.
• Ensure data integrity across dashboards and trial systems.

Skills

Project leadership

Site management

Regulatory compliance

Documentation control

Communication

Problem solving

Time management

HIPAA awareness

Bi-lingual English/Spanish

Education

Associate’s degree

Tools

Microsoft Office

Electronic health records (EHR)

Clinical trial management systems

Job description

Alcanza Clinical Research, LLC in Fredericksburg, VA, is seeking a Clinical Site Manager to oversee site operations, ensure protocol compliance, patient safety, and on-site visits within ICH/GCP guidelines. You will lead study teams, manage resources, track milestones, and partner with investigators to meet timelines and sponsor expectations.

Bi-lingual not required. This role requires an Associate’s degree and 3+ years in clinical research; leadership experience is preferred.