Clinical Research Coordinator II

Vetted Solutions; Danville (PA); On-site; USD 60,000 - 85,000; Full time

Job summary

Vetted Solutions is seeking a Clinical Research Coordinator to support multiple studies in inpatient and outpatient settings. You will coordinate study activities, prepare IRB submissions, and oversee reporting obligations under physician supervision, while interacting with patients in clinics and hospitals.

The role requires recruiting and screening participants, enrolling eligible individuals, performing nursing assessments, monitoring adverse events, and administering study drugs as directed.

Qualifications

• Requires graduation from a specialty training program; a Bachelor's Degree in Nursing is preferred.
• Strong collaboration, communication, and assessment skills are essential.

Responsibilities

• Coordinates and implements clinical research studies, preparing IRB submissions and overseeing reporting obligations.
• Responsible for trial conduct, including recruitment, screening, enrollment, and follow-up of eligible participants.
• Develops recruitment strategies, interviews subjects, and collaborates with physicians for enrollment.
• Performs nursing assessments, monitors patients for adverse events, and administers study drugs as directed.
• Reviews medical records, evaluates patient suitability for trials, and collaborates with investigators and staff.
• Creates training tools for staff, monitors lab results, and reports findings to the principal investigator.
• Informs the investigator of patient care issues, ensures proper billing, and educates staff on research protocols.
• Reviews financial statements and provides patient and family education on study protocols, risks, and benefits.
• Serves as liaison between investigators and sponsors, adapting protocols to local settings.

Skills

Collaboration

Communication

Assessment

Education

Bachelor's Degree in Nursing

Job description

Role Summary: Supports clinical research by coordinating multiple studies and trials within inpatient and outpatient settings. Assesses patient eligibility for protocols and collects data under physician supervision, including patient interactions in clinics and hospitals.

Key Responsibilities

• Coordinates and implements clinical research studies, preparing IRB submissions and overseeing reporting obligations.
• Responsible for trial conduct, including recruitment, screening, enrollment, and follow-up of eligible participants.
• Develops recruitment strategies, interviews subjects, and collaborates with physicians for enrollment.
• Performs nursing assessments, monitors patients for adverse events, and administers study drugs as directed.
• Reviews medical records, evaluates patient suitability for trials, and collaborates with investigators and staff.
• Creates training tools for staff, monitors lab results, and reports findings to the principal investigator.
• Informs the investigator of patient care issues, ensures proper billing, and educates staff on research protocols.
• Reviews financial statements and provides patient and family education on study protocols, risks, and benefits.
• Serves as liaison between investigators and sponsors, adapting protocols to local settings.

Qualifications & Skills:

Requires graduation from a specialty training program; a Bachelor's Degree in Nursing is preferred. Strong collaboration, communication, and assessment skills are essential.