Senior Clinical Research Associate - Remote

Overview

Bring your monitoring expertise to the forefront of innovation. We are looking for a Senior Clinical Research Associate (Sr. CRA) to join our A-team (remote; with travel). As a Sr. CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.

In Short

• Independently manage all aspects of monitoring for assigned clinical trials across study phases.
• Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
• Build strong site relationships, acting as a primary point of contact.
• Identify and resolve site issues, escalating as needed.
• Mentor and support junior CRAs, sharing knowledge and best practices.
• Travel throughout the United States.
• Collaborate with a supportive and experienced team.
• Contribute to the success of clinical trials.
• Work with small-medium biopharmaceutical companies.
• Help bring life-changing therapies to patients in need.

Requirements

• Experience in clinical research monitoring.
• Strong understanding of GCP and regulatory requirements.
• Excellent communication and interpersonal skills.
• Ability to manage multiple sites and trials effectively.
• Strong problem-solving skills.
• Proven mentoring capabilities.
• Willingness to travel.
• Strong organizational skills.
• Ability to work independently and as part of a team.
• Experience with data collection and site management.

Benefits

• Collaborative work environment.
• Opportunity to mentor junior team members.
• Engagement in meaningful work that impacts patients' lives.
• Supportive team culture.
• Flexibility in work arrangements.