Jr. Clinical Research Coord

jobs-americanvisionpartners; Indianapolis (IN); Presencial; USD 52 000 - 72 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Medical insurance

Dental insurance

Eye care discounts

Child care assistance

Pet insurance

Continuing education funds

401(k)

Paid holidays

PTO

Sick Time

Growth opportunities

Resumo da oferta

American Vision Partners in Phoenix seeks a Junior Clinical Research Coordinator to assist in managing clinical trials across ophthalmology practices. You will coordinate consent, enrollment, and follow-up while ensuring protocol compliance and data integrity in a dynamic clinical setting.

The role involves regulatory documentation, IRB submissions, and collaboration with investigators and study staff to deliver high-quality patient care and research outcomes.

Qualificações

• Clinical research experience in Retina or related optical care is preferred.
• Experience with regulatory documents and IRB submissions is desirable.
• GCP/IATA training or Human Subjects protection training is advantageous.

Responsabilidades

• Act as liaison between investigators, study staff, providers, IRB and sponsor.
• Screen, enroll, consent and monitor subjects per protocol with data accuracy and safety.
• Manage source documents, adverse event reporting, and regulatory filings.
• Coordinate billing for research subjects and communicate procedure costs.
• Prepare study materials for IRB submissions and audits.
• Maintain regulatory documents and attend study visits and meetings.
• Ensure adherence to protocol and accurate data entry in sponsor databases.
• Oversee drug administration, storage, and accountability; ensure patient safety.

Conhecimentos

Clinical research

Retina experience

Regulatory training

GCP/IATA training

CCRC certification

Formação académica

Associate or Bachelor’s Degree

Descrição da oferta de emprego

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 Junior Clinical Research Coordinator, you are responsible for assisting with the management and coordination of all aspects of conducting clinical trials within s RII, surgery centers, both clinically and administrative/regulatory.

Responsibilities

• Acts as a representative of clinical research and as liaison between investigators, other study staff, primary care providers, IRB and sponsor.
• Screens, consents, enrolls and follows study subjects ensuring protocol compliance and close monitoring while subjects are on study utilizing Research Nurses’ oversight for help with clinical decision making.
• Responsible for all data and source documentation, and adverse experience reporting
• Responsible for following departmental policies
• Responsible and for assuring proper billing for research subjects. Assures that charges for tests and treatments are appropriately communicated and processed.
• Assists as needed in preparing study for submission to IRB and ensures all regulatory documents are completed.
• Attends study-related meetings as appropriate.
• Travels between RCA research offices as needed for patient and business needs.
• Develops screening/enrollment/follow up mechanisms.
• Ensure adherence to protocol requirements.
• Schedules and performs patient procedures, assessments, evaluations and testing as required by the protocol, including but not limited to blood sample collection, processing and shipping, ECG, vital signs, etc., as applicable.
• Organizational maintenance of all aspects of the trial, including but not limited to timeliness in completing CRFs, reporting adverse events, managing caseload and study files.
• Responsible for quality data entry into sponsor’s database (electronic data capture systems or paper CRFs) and query resolution.
• Ensures proper study drug administration, compliance and accountability, including receipt and , storage and dispensing.
• Ensures patient safety and ensures coordination of patient care as needed.
• Assists with maintenance of regulatory documents, IRB reporting and submissions of amendments, renewals, etc.
• Assists with study initiation visits, monitoring visits, closeout visits and audit visit, ensuring all study documentation and study issues are addressed.
• Communicates regularly with the Manager of Clinical Research at RII and Principal Investigators about study related issues.
• Ensures compliance with department standards and all federal regulations and international guidelines of good clinical practice.
• Maintain job related certifications (IATA, Human subjects, subjects’ protection training, GCP, and protocol specific required training).
• Active in acquiring professional growth by obtaining CRC certification when eligible and joining a professional association such as SOCRA or ACRP.
• Performs other duties and responsibilities as required.
• Promotes a positive work environment and works to be an integral member of the team
• Encourage a team-oriented environment supporting the AVP Mission, Vision and Core Values.
• Participate in on-going training and continuing education.
• Show respect and deal appropriately with co-workers, patients, and visitors.
• Perform any and all duties assigned.

Qualifications

• Associate or Bachelor’s Degree or working toward one
• Clinical experience in Retina or other optical care
• Prior research experience
• Current IATA, Human Subjects’ protection training or GCP training highly desirable
  • Certificates, Licenses, Registrations:
• Specialty certification such as CCRC preferred

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!