Senior Clinical Research Associate - Remote

Overview

As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets, and standards of clinical research projects in a variety of therapeutic indications while focusing on subjects’ rights, safety, and well-being.

In Short

• Conduct and report onsite monitoring visits.
• Be involved in study startup.
• Perform CRF review and source document verification.
• Manage site communication and activities.
• Supervise study timelines and schedules.
• Act as a point of contact for support services and vendors.
• Participate in quality control and compliance monitoring.
• Support regulatory team with study submissions.

Requirements

• College/University degree in Life Sciences or equivalent.
• Minimum 5 years independent on-site monitoring experience in the USA.
• Experience in Phase II and/or III monitoring visits.
• Lead/Senior Monitor experience in clinical projects.
• Experience monitoring complex Oncology trials required.
• Full working proficiency in English.
• Proficiency in MS Office applications.
• Ability to plan and multitask in a dynamic environment.
• Strong communication and problem-solving skills.
• Ability to travel.

Benefits

• Advance your career in clinical research.
• Lead challenging full-service projects.
• Hands-on involvement in every aspect of the study.
• Join a company that puts its people first.