Clinical Trials Coordinator - Patient Enrollment & Protocols

ADP; City of Cortland (NY); On-site; USD 47,000 - 83,000; Full time

Job summary

Finger Lakes Medical Research is seeking an on-site Clinical Research Coordinator in Cortland, NY. This full-time role supports screening, enrollment, informed consent, and data capture for clinical trials, with duties spanning patient coordination, protocol adherence, and data integrity.

The position emphasizes collaboration with investigators, meticulous data handling, and accurate dose calculations, with the goal of meeting recruitment targets and ensuring protocol compliance.

Qualifications

• Must possess good communication and interpersonal relationship skills.
• Must be able to organize work with minimal supervision.
• Must be able to focus attention to minute details.
• Access, Work and Excel computer skills required.

Responsibilities

• Coordinate screening and enrollment of clinical trial patients.
• Review physician-patient schedules and assess enrollment suitability.
• Educate patients and families during informed consent.
• Register patients to protocols and ensure eligibility.
• Ensure protocol-required patient testing is ordered and complete.
• Maintain recruitment strategies and market protocols to meet goals.
• Coordinate clinical trial activities at the clinic and hospital.
• Verify source documents and data submissions.
• Collaborate with investigators on protocol compliance.
• Interview patients for adverse events and outcomes.
• Obtain follow-up data after active treatment ends.
• Maintain drug accountability records and accurate dosing.

Skills

Communication skills

Interpersonal skills

Organizational skills

Attention to detail

MS Access

MS Excel

Tools

MS Word

Job description

Finger Lakes Medical Research is seeking an on-site Clinical Research Coordinator in Cortland, NY. This full-time role supports screening, enrollment, informed consent, and data capture for clinical trials, with duties spanning patient coordination, protocol adherence, and data integrity.

The position emphasizes collaboration with investigators, meticulous data handling, and accurate dose calculations, with the goal of meeting recruitment targets and ensuring protocol compliance.