Associate Site Director - Vision Research Center

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Regular Full-Time Vision Research Center, Albuquerque, NM, US

Full-time/On-site

Take the next step in your clinical research career and help lead the future of eye care.

Eye Associates of New Mexico is seeking an experienced and highly motivated Associate Site Director to join our Vision Research Center
. This is an exciting leadership opportunity for a clinical research professional who is passionate about advancing patient care, developing high-performing teams, and ensuring excellence in clinical trial operations.

Working closely with the Director of the Vision Research Center, you’ll help oversee clinical research site operations and provide leadership to a multidisciplinary team that may include physician investigators, Clinical Research Coordinators, vision examiners, photographers, and laboratory technicians. You’ll also play an important role in regulatory compliance, patient safety, data integrity, study implementation, and the continued growth of our research program.

As the Associate Site Director, you’ll help lead clinical research operations while ensuring studies are conducted safely, effectively, and in accordance with applicable regulations and protocols.

Responsibilities include:

• Support the Director of the Vision Research Center in all aspects of clinical research site operations
• Provide leadership and guidance to members of the clinical research team
• Help lead complex clinical trials, including recruitment, care, and treatment of research participants
• Ensure adherence to study protocols, procedures, standards, and research best practices
• Promote compliance with FDA, ICH, GCP, CFR, and applicable regulatory requirements
• Support investigators in the implementation and execution of clinical research
• Help ensure the highest standards of patient safety and clinical research data integrity
• Provide guidance regarding HIPAA, informed consent, confidential patient records, and sponsor proprietary information
• Collaborate across departments to successfully initiate and conduct clinical trials
• Support Institutional Research Investigators with investigator-initiated clinical trials and informed consent documents
• Apply knowledge of IRB requirements and regulatory processes to research operations
• Assist in identifying and developing new business opportunities for the Vision Research Center
• Recruit, evaluate, educate, and provide instruction to clinical research participants
• Collect, maintain, evaluate, and safeguard clinical research data and study records
• Make administrative and procedural decisions involving sensitive and confidential matters
• Help maintain quality, safety, and infection-control standards
• Represent the research program professionally with investigators, sponsors, patients, colleagues, and other stakeholders

The position requires strong clinical-trial experience and the ability to serve as a team leader for complex studies while maintaining compliance with FDA, ICH and GCP requirements.

This role is ideal for an experienced clinical research professional who combines strong clinical knowledge with leadership, communication, and operational skills.

Qualifications include:

• Bachelor’s degree from an accredited school in a medical or related field, such as nursing, ophthalmology, biology, or a related discipline
  - Required
• Significant directly related clinical experience
• Clinical Research Coordinator (CRC) experience
• Clinical research management experience
• Strong clinical trials experience and demonstrated…