Clinical Research Coordinator

jobs-americanvisionpartners; Indianapolis (IN); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Eye care discounts

401(k)

Paid holidays

PTO

Sick Time

Continuing education funds

Job summary

American Vision Partners (AVP) seeks a Clinical Research Coordinator to oversee and facilitate clinical research activities across affiliated eye care practices. You will coordinate protocol procedures, screen and enroll participants, and manage study visits with emphasis on participant safety and regulatory compliance.

The role requires at least 1 year of clinical research experience, an associates or allied health degree, and strong communication skills.

Qualifications

• Associates Degree or allied health professional degree or equivalent.
• At least 1 year clinical research experience to include consenting patients.
• Basic understanding of regulatory binders highly preferred.
• Ability to adhere to Good Clinical Practices, FDA, HIPAA, IRB regulation, and principles of research design.
• Detail oriented, reliable and able to multi-task in a fast-paced, high-volume work environment.
• Excellent verbal and written communication skills.
• Personable; empathetic with subject's needs and concerns.
• Flexible schedule working Monday–Friday.
• Occasional travel to other RCA location in Metro Valley.

Responsibilities

• Coordinates protocol related research procedures, study visits, and follow-up care
• Screens, recruits, and enrolls patients/research participants
• Schedules patient/research participants visits and procedures
• Independently completes the informed consent process of study subjects
• Educates research participants and family on protocol, study intervention, study drug/device, etc.
• Conducts vital signs
• Collects, processes, and ships laboratory specimens
• Administers questionnaires
• Supports the safety of clinical research procedures, study visits, and follow-up care
• Submits documents to regulatory authorities (IRB, FDA, etc.) and/or review/monitoring boards
• Facilitates study close out activities
• Retains records and archives documents after conclusion of study
• Completes case report forms and address queries
• Develops and maintains source documents
• Performs additional duties as assigned

Skills

Clinical research coordination

Regulatory compliance

Good Clinical Practices

HIPAA

Communication skills

Multitasking

Education

Associates Degree or allied health degree

Job description

Company Intro

AtAmerican Vision Partners (AVP), we partner with the most respected ophthalmology practices in the country and integrate best-in-class management systems, operational infrastructure, and advanced technology to provide the highest quality patient care possible. Our practices include Barnet Dulaney Perkins Eye Center, Southwestern Eye Center, Retinal Consultants of Arizona, M&M Eye Institute, Abrams Eye Institute, Southwest Eye Institute, Aiello Eye Institute, Moretsky Cassidy Vision Correction, Wellish Vision Institute, West Texas Eye Associates and Vantage Eye Center. We are focused on building the nation’s largest and most comprehensive eye care practices and currently operate more than 100 eye care centers in Arizona, New Mexico, Nevada, California and Texas – including 25 ambulatory surgical centers. At AVP we value teamwork, providing exceptional experiences, continuous improvement, financial strength, and hard work. We are committed to providing best-in-class patient care, pioneering research and technology, and most importantly, rewarding and recognizing our employees!

Overview

As a Clinical Research Coordinator, you’ll oversee and facilitate the clinical research activities.

Responsibilities

• Coordinates protocol related research procedures, study visits, and follow-up care
• Screens, recruits, and enrolls patients/research participants
• Schedules patient/research participants visits and procedures
• Independently completes the informed consent process of study subjects
• Educates research participants and family on protocol, study intervention, study drug/device, etc.
• Conducts vital signs
• Collects, processes, and ships laboratory specimens
• Administers questionnaires
• Supports the safety of clinical research procedures, study visits, and follow-up care
• Submits documents to regulatory authorities (IRB, FDA, etc.) and/or review/monitoring boards
• Facilitates study close out activities
• Retains records and archives documents after conclusion of study
• Completes case report forms and address queries
• Develops and maintains source documents
• Performs additional duties as assigned

Qualifications

• Associates Degree or an allied health professional degree or equivalent
• At least 1 year clinical research experience to include consenting patients
• Basic understanding of regulatory binders highly preferred
• Ability to adhere to Good Clinical Practices, FDA, HIPPA, IRB regulation, and principal of research design
• Detail oriented, reliable and able to multi-task in a fast-paced, high-volume work environment
• Excellent verbal and written communication skills
• Personable; empathetic with subject's needs and concerns
• Ability to maintain confidentiality and professionalism
• Flexible schedule working Monday-Friday
• Occasional travel to other RCA location in Metro Valley.

Benefits & Perks

Your health, happiness and your future matters! At AVP, we offer everything from medical and dental insurance, significant eye care discounts, child care assistance, pet insurance, continuing education funds, 401(k), paid holidays, PTO, Sick Time, opportunity for growth, and much more!