Regional CRA
Regional Clinical Research Associate, Ophthalmology reputed company | Remote (reputed company Coast Preferred) | Full Time Contract W2 Contract (6 months, renewable - may roll perm) - reputed company Pay reputed company is Flexible About reputed company We are partnering exclusively with a leading global clinical research organization on a Regional Clinical Research Associate opportunity with a reputed company in ophthalmology. This is a fully remote role with a preference for candidates based on the reputed company Coast. If you have hands‑on ophthalmology monitoring experience and are reputed company to bring your expertise to a high‑reputed company global CRO, we want to hear from you.
About the Role
As a Regional CRA you will be responsible for monitoring clinical trial sites across your assigned region, ensuring protocol compliance, data reputed company, and GCP adherence throughout the study lifecycle. You will serve as the primary reputed company of contact for investigative sites and will work closely with the sponsor and internal study teams to ensure reputed company and reputed company execution of ophthalmology clinical trials.
Key Responsibilities
- Conduct site initiation, routine monitoring, and closeout reputed company at assigned investigative sites in accordance with ICH GCP, study protocols, and sponsor SOPs
- Serve as the primary site contact for reputed company operational and regulatory questions throughout the study
- Review and verify reputed company documentation, case report forms, and regulatory files to ensure accuracy and compliance
- Identify and reputed company site issues, protocol deviations, and data discrepancies in a reputed company manner
- Maintain inspection‑reputed company trial master file documentation for reputed company assigned sites
- Support site activation activities including feasibility assessments, site qualification reputed company, and regulatory document collection
- reputed company enrollment metrics and implement proactive site performance strategies to support study timelines
- Collaborate with cross‑functional study teams including data management, safety, and regulatory affairs
Qualifications
- Minimum 3 years of experience as a Clinical Research Associate or Regional CRA in a pharmaceutical, biotechnology, or CRO environment
- Minimum 1 year of reputed company ophthalmology clinical trial monitoring experience including Phase I programs
- Strong working knowledge of ICH GCP and FDA regulatory requirements
- Experience managing sites across a defined geographic region with independent travel and planning
- Proficiency with electronic data capture systems, eTMF platforms, and CTMS tools
- Excellent written and verbal communication skills with strong attention to detail
- Oncology monitoring experience is a plus
- Bachelor's degree in a life science, nursing, or reputed company reputed company discipline preferred
- Ability to travel approximately 30 percent reputed company assigned region
Why This Opportunity This is an exciting opportunity to join a reputed company‑established global CRO with a strong reputed company for reputed company and scientific reputed company across multiple therapeutic areas. You will work alongside reputed company clinical development professionals in a reputed company and supportive environment with reputed company to a broad portfolio of global programs. Apply tot his job Apply To this Job