Vision Research Center – Associate Site Director

Eyenm; Albuquerque (NM); On-site; USD 120,000 - 170,000; Full time

Benefits offered by this job

Paid Time Off (PTO)

401(k)

Education Assistance

Company-paid Life Insurance

Company-paid AD&D Insurance

Job summary

Eye Associates of New Mexico seeks an experienced Associate Site Director for the Vision Research Center in Albuquerque. You will oversee multidisciplinary clinical research operations, lead a team of investigators, coordinators, and staff, and ensure strict adherence to regulatory standards and study protocols.

You will collaborate with the Center Director to grow the research program, manage data integrity and patient safety, and support investigator-initiated trials, informed consent

Qualifications

• Bachelor’s degree in a medical-related field (nursing, ophthalmology, biology, etc.).
• Five years of directly related clinical experience.
• Five years of management experience.
• CRC experience or certification.
• ARCP certification required.
• Familiarity with FDA, ICH, and GCP regulations.
• Knowledge of IRB requirements and procedures.
• Strong leadership and decision-making abilities.

Responsibilities

• Lead clinical research site operations with safety and protocol compliance.
• Provide leadership to the clinical research team and investigators.
• Oversee recruitment, care, and treatment of research participants.
• Ensure study protocols, procedures, and data integrity are upheld.
• Coordinate regulatory compliance, patient safety, and sponsor communications.
• Collaborate across departments to initiate and conduct trials.
• Support investigator-initiated studies and informed consent processes.

Skills

Leadership

Regulatory compliance

Clinical trial operations

Team management

Communication skills

Education

Bachelor’s degree in medical field

Job description

Eye Associates of New Mexico seeks an experienced Associate Site Director for the Vision Research Center in Albuquerque. You will oversee multidisciplinary clinical research operations, lead a team of investigators, coordinators, and staff, and ensure strict adherence to regulatory standards and study protocols.

You will collaborate with the Center Director to grow the research program, manage data integrity and patient safety, and support investigator-initiated trials, informed consent