On-Site Associate Site Director, Vision Research Center

Eye-Associates-of-New-Mexico; Albuquerque (NM); Sur place; USD 120 000 - 170 000; Plein temps

Avantages offerts par ce poste

Paid Time Off (PTO)

8 paid holidays

401(k)

Education Assistance

Company-paid Life Insurance

Company-paid AD&D Insurance

And more!

Résumé du poste

Eye Associates of New Mexico is seeking an experienced Associate Site Director to lead the Vision Research Center in Albuquerque. This leadership role oversees clinical research site operations, regulatory compliance, and a multidisciplinary team to advance patient care.

You will guide investigators and staff, manage complex trials, ensure safety and data integrity, and pursue new opportunities to grow the research program.

Qualifications

• Bachelor’s degree required in a medical or related field (nursing, ophthalmology, biology, or similar).
• At least five years of directly related clinical experience and five years in management.
• CRC experience and certification preferred.
• Strong knowledge of FDA/ICH/GCP regulations and IRB processes.
• Supervisory experience and ability to lead a multidisciplinary team.

Responsabilités

• Lead clinical research site operations in the Vision Research Center.
• Provide leadership and guidance to clinical research staff.
• Oversee recruitment, care, and treatment of research participants.
• Ensure adherence to study protocols, standards, and best practices.
• Maintain patient safety and data integrity; ensure regulatory compliance.
• Develop new research opportunities and sponsor relationships.
• Represent the program with investigators, sponsors, and stakeholders.

Connaissances

Leadership

Regulatory knowledge

Clinical research

Team management

Communication skills

Formation

Bachelor’s degree in medical or related field

Description du poste

Eye Associates of New Mexico is seeking an experienced Associate Site Director to lead the Vision Research Center in Albuquerque. This leadership role oversees clinical research site operations, regulatory compliance, and a multidisciplinary team to advance patient care.

You will guide investigators and staff, manage complex trials, ensure safety and data integrity, and pursue new opportunities to grow the research program.