Global Alzheimer's Platform Foundation · 1 day ago
Senior Clinical Research Coordinator
Tampa, FL
Full-time
Onsite
Mid, Senior Level
$65K/yr - $80K/yr
3+ years expGlobal Alzheimer's Platform Foundation is seeking a Senior Clinical Research Coordinator to manage and coordinate clinical research studies focused on Alzheimer's and other neurodegenerative diseases. The role involves ensuring compliance with regulatory standards, overseeing participant safety, and mentoring junior staff while maintaining high-quality data collection.
Health CareNon ProfitWellness
Responsibilities
Independently coordinates multiple clinical research studies across varying therapeutic areas and phases
Reviews study protocols and identifies operational needs, feasibility, and required resources
Schedules and conducts participant study visits, collects research data, and manages required study procedures per protocol
Ensures compliance with protocol, IRB regulations, institutional policies, FDA regulations, and ICH-GCP guidelines
Conducts informed consent discussions and ensures documentation aligns with ALCOA-C practices
Monitors participant safety, documents adverse events, and communicates with Principal Investigator (PI) and sponsor, as required
Supports participant retention through timely follow-up, visit reminders, and engagement
Knowledgeable in how to prepare, submit, and maintain regulatory documents, IRB submissions, and continuing reviews
Maintains accurate and timely source documentation, case report forms (CRFs), and study files
Ensures investigational product (IP) accountability and compliance in collaboration with pharmacy or designated site staff managing the IP
Performs data entry and query resolution in electronic data capture (EDC) systems within the contracted timeline
Participates in investigator meetings (IM), site selection visits (SSV), site initiation visits (SIV), sponsor monitoring visits, audits, inspections and quality review processes
Identifies deviations and contributes to corrective and preventive action planning
Serves as a resource and mentor to junior level staff members including but not limited to Clinical Research Coordinators and Research Assistants
Assists in training new staff on site operating procedures (SOP), study specific protocol procedures, documentation standards, and compliance expectations
Collaborates effectively with investigators, clinical teams, sponsors, CROs, and regulatory personnel
Qualification
Required
Bachelor's degree in a health-related or scientific field; or equivalent clinical research experience
Minimum 3–5 years of clinical research coordination experience
Strong knowledge of ICH-GCP, Good Documentation Practices (GDP)/ALCOA-C, and clinical research regulatory requirements
Experience conducting informed consent, coordinating study visits, and managing CRFs/EDC systems independently
Preferred
Certification in Clinical Research (e.g., CCRC, CCRP, ACRP-CP)
Spanish Speaker
Experience with multiple therapeutic areas or complex interventional trials
Familiarity with FDA inspections or sponsor audits
Benefits
Health insurance
Retirement savings
Paid time off
Professional development opportunities
Company
Global Alzheimer's Platform Foundation
Global Alzheimer's Platform Foundation aims to reduce the time, cost, and risk of Alzheimer’s clinical trials.
11-50 employees
Funding
Current Stage
Early StageLeadership Team
John R. Dwyer
President
Recent News
Longevity.Technology
2026-01-20
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