Sr. Clinical Research Associate

📋 Description

• Oversee clinical site monitoring and management across studies (onsite and remote).
• Coordinate site qualification, initiation, routine monitoring, and close-out visits.
• Ensure activities comply with SOPs, study plans, ICH-GCP, and local regulations.
• Review data against source documentation; resolve data queries and issues.
• Monitor and facilitate shipment of clinical supplies and study documents.
• Train site staff on protocols, systems, and ICH-GCP requirements.

🎯 Requirements

• 4–6 years of relevant clinical research experience; 7–9 years preferred.
• Bachelor’s degree in Health/Life Sciences, Pharmacy, Nursing or related; Master’s advantageous.
• Senior CRA or ACRP certification a plus.
• Strong knowledge of ICH-GCP and local regulatory requirements.
• Experience with Phase I–IV trials; proficient with EDC (Medidata Rave, Oracle InForm), IRT, eTMF
• Fluent English; valid driver’s license; ability to travel ~40–60%.

🎁 Benefits

• Salary: $58,000–$96,500 per year (depends on experience, location).
• Home-based work; regular travel to clinical sites and meetings.
• Professional growth and mentoring opportunities in clinical research.
• Cross-functional collaboration with sponsors, investigators, and regulatory teams.
• Opportunity to contribute to process improvements and best practices.