Clinical Feasibility Coordinator — Multi-Site Trials

Alcanza Clinical Research; Town of Florida (NY); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

Medical, dental, vision

401k with safe harbor match

Life and disability insurance

Job summary

Alcanza Clinical Research seeks a Feasibility Coordinator to advance clinical study feasibilities across multiple sites. You will support the Business Development team by identifying investigators, reviewing protocols, and maintaining site capability documentation.

The role requires a high school diploma with at least 2 years of administrative or related experience; clinical research experience and bilingual English/Spanish are a plus.

Qualifications

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

Responsibilities

• Complete feasibility in accordance with set timelines per sponsor/Clinical Research Organization (CRO) requirements.
• Review and understand study details such as protocol for feasibility.
• Identify potential investigators at sites with Business Development Team.
• Contact potential investigators to discuss study details and assess feasibility.
• Maintain documentation as to sites capabilities, including equipment lists (MRI, PET, CSF, etc.).
• Submit feasibility questionnaires and update feasibility regularly.
• Input PI information into Sponsor, CRO and databases.
• Assist in managing upcoming research trials pipeline.
• Attend and complete company training programs and meetings.
• Communicate with clients and stakeholders professionally.

Skills

Administrative support

Organization

Communication

Bilingual English/Spanish

HIPAA awareness

Education

High school diploma or equivalent

Tools

Microsoft Office

EHR systems

Web applications

Job description

Alcanza Clinical Research seeks a Feasibility Coordinator to advance clinical study feasibilities across multiple sites. You will support the Business Development team by identifying investigators, reviewing protocols, and maintaining site capability documentation.

The role requires a high school diploma with at least 2 years of administrative or related experience; clinical research experience and bilingual English/Spanish are a plus.