Senior Clinical Research Associate at Catalyst Clinical Research Full Time NEW

Responsibilities

• Monitor clinical trials to achieve project goals.
• Travel up to 80% within an assigned territory.
• Conduct site evaluations, study initiations, and close-outs.
• Communicate with site staff and report study status.
• Resolve study-related issues and audit findings.
• Assist with Investigator Meetings and FDA submission prep.
• Manage work activities to meet budget and timelines.
• Participate in meetings to stay updated on regulations.
• Collaborate with Study Manager and Project Manager.
• Provide internal support to Field Monitor.

Requirements

• Bachelor’s degree in a science or health-related field.
• 7 years industry experience or equivalent.
• Minimum 5 years in clinical research with monitoring experience.
• 3 years recent oncology clinical trial experience required.
• Strong knowledge of regulatory compliance and trial methodology.
• Excellent organizational and time management skills.
• Strong communication and interpersonal skills are essential.
• Flexibility to travel routinely for project requirements.
• Proficient in standard computer applications.

Benefits

• Equal opportunity employer committed to diversity.
• Inclusive environment for all employees.