We are seeking experienced Ophthalmology (Sr CRAs & CRA 1/2) to lead and support our Full Service Outsourcing team, with flexibility for major hub locations in the U.S. This role involves 60-70% travel and 8-10 days of service per month.
Key responsibilities include:
- Managing all aspects of study site monitoring, including routine visits, site close-outs, study file maintenance, and vendor liaison.
- Overseeing site management in accordance with project plans.
- Ensuring proper training and safety procedures for study staff.
- Verifying informed consent and protocol adherence to protect study participants.
- Monitoring data integrity, reviewing CRFs, and resolving discrepancies.
- Handling SAE reporting, generating reports, and following up.
- Assisting with training new employees and coordinating clinical projects as a Local Project Coordinator.
Qualifications and skills:
- University or college degree, or certification in a related health profession (e.g., nursing license).
- 1-3 years of clinical monitoring experience.
- Comfort working in a fast-paced environment with changing priorities.
- Strong teamwork, communication, and technology skills, with experience working in electronic data collection.
Additional details:
- Competitive compensation and comprehensive benefits including health insurance, 401(k), PTO, and employee recognition.
- Work performed in an office environment with frequent travel, domestic and international.
- Physical ability to sit, operate a vehicle, lift objects up to 20 lbs., and access various software.
This role offers an engaging environment focused on high-quality clinical research and teamwork.