Description
We are seeking experienced Clinical Research Associates (CRAs) with Ophthalmology monitoring experience to join our team. As a CRA, you will be responsible for monitoring clinical trials, ensuring compliance with regulations and good clinical practice.
Responsibilities:
- Conduct routine monitoring and close-out of clinical sites
- Maintain study files and ensure data integrity
- Liaise with vendors and study site staff
- Ensure the protection of study patients by verifying informed consent procedures and protocol requirements
- Verify data submitted on Case Report Forms (CRFs) or other data collection tools
- Complete Serious Adverse Event (SAE) reporting and follow-up
- Independently perform CRF review and query generation
- Assist with training of new employees
- Coordinate designated clinical projects as a Local Project Coordinator
Requirements:
- University or college degree, or certification in a related allied health profession (e.g., nursing licensure)
- 4+ years of Clinical Monitoring experience (Sr. CRA level)
- Ophthalmology experience is required
- 60-70% overnight travel
Work Environment:
- Fast-paced environment with changing priorities
- Teamwork and people skills are essential
- Technology-based environment with electronic data collection
Physical Requirements:
- Ability to sit for extended periods and operate a vehicle safely
- Repetitive hand movement and ability to make fast, simple, repeated movements
- Occasional crouching, stooping, and bending
- Ability to access and use various computer software
- Light to moderate lifting and carrying (up to 15-20 lbs)
Salary: $110,000 - $145,000 per year