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Senior Clinical Research Coordinator - Job Opportunity at Center for Advanced Research & Education

Gainesville, United States
Full-time
Senior
Posted: March 30, 2025
On-site
USD 25.00 per hour

Benefits

Comprehensive health insurance with competitive coverage
Flexible scheduling arrangements supporting work-life balance
Paid time off package indicating investment in employee wellbeing

Key Responsibilities

Lead clinical study execution according to FDA regulations and GCP guidelines
Design and implement organizational systems for study compliance and accuracy
Ensure subject safety and protocol adherence while managing study documentation
Train and coordinate with medical staff on protocol implementation
Manage subject screening, consent processes, and visit scheduling
Maintain detailed case histories and accurate CRF/eCRF documentation
Coordinate with sponsors and manage clinical supplies

Requirements

Education

Medical Assistant, Pharmacy Technician, Bachelor's Degree, or Master's Degree

Experience

Prior patient-related experience in medical facility or pharmacy required

Required Skills

Protocol compliance FDA regulations knowledge GCP guidelines expertise Clinical documentation Subject safety management Staff training Data entry accuracy Communication skills
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Sauge AI Market Intelligence

Industry Trends

Clinical research sector is experiencing rapid growth due to increased drug development and medical device trials, particularly in response to emerging health challenges. Digitalization of clinical trials is driving demand for coordinators with strong technical competencies in eCRF systems and digital documentation. Rising complexity in trial protocols is elevating the importance of experienced coordinators who can ensure compliance while maintaining efficiency.

Salary Evaluation

USD 52,000 - 75,000 annually based on location and experience level, which aligns with industry standards for senior clinical research positions in secondary markets

Role Significance

Typically works within a team of 3-7 clinical research staff, often serving as a lead coordinator
Senior-level position with significant autonomy in study coordination and staff training responsibilities

Key Projects

Phase I-IV clinical trials management Protocol implementation and staff training programs Regulatory compliance initiatives Subject safety monitoring systems development

Success Factors

Strong attention to detail and organizational skills for managing complex study requirements Excellent communication abilities for effective interaction with subjects, sponsors, and medical staff Deep understanding of regulatory requirements and ability to ensure compliance Capacity to manage multiple studies while maintaining accuracy and timeline adherence

Market Demand

High demand with steady growth projected due to increasing clinical trial volumes and complexity of studies

Important Skills

Critical Skills

Regulatory compliance expertise - Essential for maintaining study integrity and legal requirements Clinical documentation proficiency - Critical for accurate data collection and study validity Subject safety management - Fundamental to ethical research conduct

Beneficial Skills

Project management capabilities Statistical analysis understanding Electronic data capture system expertise

Unique Aspects

Combination of clinical expertise and research management responsibilities
Focus on both operational excellence and regulatory compliance
Opportunity to impact medical research advancement directly

Career Growth

2-4 years in current role before advancement, depending on performance and organizational growth

Potential Next Roles

Clinical Research Manager Clinical Operations Director Clinical Trial Manager Research Site Manager

Company Overview

Center for Advanced Research & Education

Research-focused organization specializing in clinical trials and advanced medical research

Regional research center contributing to medical advancement through clinical studies
Significant presence in the Southeast medical research community
Professional environment with emphasis on accuracy, compliance, and subject safety
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