Clinical Research Coordinator I

Ora • Andover, MA

316d

About The Position

At Andover Eye Institute, our mission is to lead the future of eye care through innovative clinical trials and groundbreaking research. We are committed to advancing the understanding and treatment of ophthalmic conditions by exploring new frontiers in medical science. Our team of experienced and compassionate professionals works closely with participants and sponsors, ensuring that each clinical trial is conducted with the utmost care, precision, and attention to detail. The Andover Eye Institute Per Diem, Clinical Research Coordinator I (CRC I) has close relationships with the subjects who participate in our clinical trials. Our CRC I's will collect, record, and organize research information for clinical projects, while ensuring compliance with clinical project protocol and overall clinical objectives. Our CRC I's will partner with Clinical Research Coordinators and Clinical Project Managers to execute protocol directives and work cross-functionally with internal and external teams such as other Research Coordinators and Investigators.

Requirements

• Bachelor's degree in Life Sciences or 1-year experience in a clinical or lab setting including course work.
• Previous experience as a research coordinator strongly preferred.
• Certified Ophthalmic Associate or Certified Ophthalmic Technician certifications strongly preferred.
• Advanced degree in related study preferred but not required.
• Medical skills and/or certifications such as (CPT) certified phlebotomist technician, (EMT) Emergency Medical Technician preferred.
• The ability to work a flexible schedule including weekends.
• A team player attitude with a strong interest in clinical studies and enjoy interacting with patients.

Responsibilities

• Performs clinical skills identified in the SOP at study visits.
• Maintains protocol compliance during clinical projects.
• Be compliant with SOP, ICH-GCP and regulations.
• Login time and expenses in a timely manner, follow the guidelines and company expense policy.
• Participates in study start-up activities such as putting together charts, pulling patient charts, ensuring site cleanliness.
• Performs patient screening, recruitment, and enrollment.
• Create study documents as assigned.
• Maintains study documents, including source documentation, case report forms, and regulatory documentation.
• Provide Quality Control of documents as required.
• Enters data into electronic database and resolves data queries.
• Adhere to all aspects of Andover Eye Institute quality system.
• Adhere to all essential systems and processes that are required at Andover Eye Institute to maintain compliance to Andover Eye Institute data integrity & business ethics and regulatory requirements.
• Clear and sustained demonstration of Andover Eye Institute values -- prioritizing kindness, operational excellence, cultivating joy and scientific rigor - as well as their linked behaviors.
• Responsibilities may differ from the above based on the specific needs of the business.

Benefits

• Diverse workforce encouraged to apply.
• Affirmative Action and Equal Opportunity Employer.

What This Job Offers

• Industry: Ambulatory Health Care Services
• Education Level: Bachelor's degree
• Number of Employees: 51-100 employees