Clinical Research Feasibility Coordinator — Growth & Impact

Accel Research Sites; Florida; On-site; USD 52,000 - 70,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401k plan with match

Job summary

Accel Research Sites is seeking a Clinical Research Feasibility Coordinator to join the Business Development team at our Alcanza Corporate location. You will coordinate feasibility activities across multiple sites and assist in building a robust pipeline for upcoming trials.

Responsibilities include evaluating protocol details, identifying investigators, and maintaining documentation in CRM/system records while complying with HIPAA and quality standards.

Qualifications

• Must have a high school diploma or equivalent and 2+ years of administrative or sales support experience, or an equivalent combination.
• 1+ years of clinical research experience is required.
• Bi-lingual (English/Spanish) proficiency is a plus.

Responsibilities

• Process feasibilities within set sponsor/CRO timelines.
• Identify potential investigators and sites for studies with the Business Development team.
• Contact and discuss study details with investigators to assess feasibility.
• Maintain site capability documentation and CRM records.
• Input PI information into Sponsor/CRO databases and assist with confidential agreements.

Skills

Microsoft Office

Communication

Organizational skills

Attention to detail

HIPAA knowledge

Independence

Education

High school diploma or equivalent

Tools

EHR systems

CRM

Job description

Accel Research Sites is seeking a Clinical Research Feasibility Coordinator to join the Business Development team at our Alcanza Corporate location. You will coordinate feasibility activities across multiple sites and assist in building a robust pipeline for upcoming trials.

Responsibilities include evaluating protocol details, identifying investigators, and maintaining documentation in CRM/system records while complying with HIPAA and quality standards.