You will get Clinical Research Patient Recruitment & Prescreening Support
Project details
Clinical Research Coordinator and Clinical Operations Specialist with hands-on experience supporting pulmonology and dermatology clinical trials in private research sites. Experienced in patient recruitment, prescreening, workflow organization, source documentation, EDC support, study coordination, sponsor communication, and operational research support.
I help research sites improve organization, streamline workflows, and reduce operational inefficiencies while maintaining high-quality standards. My approach is proactive, detail-oriented, and focused on practical solutions that support smoother study execution and stronger site performance.
Services may include patient recruitment support, eligibility review, workflow organization, study startup assistance, research tracking systems, source documentation support, and remote clinical research coordination.
Bilingual: English & Spanish.
I help research sites improve organization, streamline workflows, and reduce operational inefficiencies while maintaining high-quality standards. My approach is proactive, detail-oriented, and focused on practical solutions that support smoother study execution and stronger site performance.
Services may include patient recruitment support, eligibility review, workflow organization, study startup assistance, research tracking systems, source documentation support, and remote clinical research coordination.
Bilingual: English & Spanish.
Purpose
BusinessIndustry
Medical & PharmaceuticalLanguage
EnglishWhat's included $300
These options are included with the project scope.
$300
- Delivery Time 5 days
- Number of Revisions 1
- Number of Hours of Work 5
- Summary
About Maria
Clinical Research Operations Consultant | Site Growth & Enrollment
Davie, United States - 11:54 pm local time
My experience includes patient recruitment and prescreening, source documentation creation, EDC data entry, regulatory support, visit coordination, sponsor communication, workflow optimization, and operational support across multiple clinical studies.
I specialize in improving site organization, streamlining research workflows, and helping research teams reduce operational bottlenecks while maintaining high-quality standards.
I have experience supporting:
Pulmonology clinical trials
Dermatology clinical trials
Patient recruitment and prescreening
Eligibility review and chart analysis
Source document creation
EDC data entry and query resolution
Regulatory document organization
Study startup support
Research operations coordination
Sponsor and CRA communication
Bilingual: English & Spanish
Available for:
Remote Clinical Research Coordinator support
Clinical trial operations assistance
Patient recruitment and prescreening
Source documentation and data entry
Research workflow organization
Site operational support
Steps for completing your project
After purchasing the project, send requirements so Maria can start the project.
Delivery time starts when Maria receives requirements from you.
Maria works on your project following the steps below.
Revisions may occur after the delivery date.
Receive the list of problems from the client