What are the responsibilities and job description for the Clinical Research Coordinator position at Eye Associates Of New Mexico?
Clinical Research Coordinator
Eye Associates of New Mexico has an outstanding career opportunity in our Vision Research Department.
Eye Associates of New Mexico is the largest Ophthalmology and Optometry practice in the Southwest. We serve our communities with compassionate, state-of-the-art and value-based care. Our team approach aims to deliver the highest quality eye care to all. We take pride in providing the absolute highest level of patient care through our employees, and we strive to support their professional development.
We are currently looking for a full-time Clinical Research Coordinator, to join our Vision Research team. If you are detail-oriented, passionate about advancing patient care through clinical research, and enjoy working in a collaborative healthcare environment, we encourage you to apply. Come be a part of our team and help make a difference in our patients' vision.
Some Job Duties May Include:
- Coordinate clinical research studies under the direction of the Principal Investigator and Vision Research leadership
- Maintain accurate study documentation, subject records, and source documents
- Perform study-related procedures in accordance with research protocols, Good Clinical Practice (GCP), ICH, and FDA guidelines
- Screen, recruit, enroll, and retain study participants while ensuring protocol compliance
- Collect medical histories, concomitant medications, and study-specific clinical data
- Enter and maintain study data within sponsor electronic data capture (EDC) systems
- Prepare for sponsor site visits, audits, and regulatory inspections
- Assist with Institutional Review Board (IRB) submissions and regulatory documentation
- Coordinate specimen collection, processing, storage, and shipment as required
- Communicate with physicians, study sponsors, regulatory agencies, and research participants
- Support adverse event documentation and follow-up
- Maintain HIPAA compliance and ensure confidentiality of research participants
- Assist with scheduling research visits and providing ongoing patient education
Skills/Requirements:
- Prior clinical research experience or Certified Clinical Research Coordinator (CCRC) certification preferred
- Strong attention to detail with accurate data entry skills
- Experience working within sponsor electronic data systems is preferred
- Ability to maintain screening and recruitment logs using Excel or Microsoft Word
- Strong organizational, communication, and critical thinking skills
- Phlebotomy experience preferred
- Ophthalmology experience or COA, COT, or COMT certification is a plus, but not required
Generous Benefits:
- Paid Time Off (PTO)
- Eight (8) Company Paid Holidays
- Medical and Dental Insurance
- Generous Vision Benefits
- Flexible Spending Accounts (FSA)
- Company-Paid Life and AD&D Insurance
- Voluntary Supplemental Life and AD&D Insurance
- Employee Assistance Program (EAP)
- 401(k) and Roth Retirement Plans
- Financial Wellness Program
- And much more!
Eye Associates of New Mexico is proud to foster a safe, team-oriented culture that supports a drug-free workplace.
To learn more about this position and our organization, please visit www.eyenm.com.
AA/EOE/Disability. Eye Associates of New Mexico is a drug and tobacco-free employer.
Req # 2900