Clinical Research Associate Manager

Key Responsibilities:-

• Oversee CRA performance, development, and coaching to ensure delivery, productivity, and quality performance indicators
• Manage and allocate CRA resources to studies and sites, ensuring balanced workloads and quality monitoring
• Monitor and approve CRA travel and expenses to ensure compliance with T&E policy and budget
• Collaborate with SSO Clinical Project Managers to support recruitment strategies and site performance
• Ensure timely communication with vendors and align resource needs and expectations
• Oversee vendor monitoring performance targets, including site recruitment commitments, timely data entry, and issue resolution
• Support clinical development audits, site audits, and inspections, ensuring CAPA follow-up and implementation.

Essential Requirements :-

• A degree in a scientific or health discipline; an advanced degree is preferable
• Minimum 7 years of experience in clinical research, including planning, executing, and monitoring clinical trials
• Strong project management and team leadership capabilities
• Thorough understanding of clinical drug development, international standards (GCP/ICH), and health authority regulations
• Excellent communication, negotiation, and conflict resolution skills
• Ability to travel domestically and internationally as needed
• Proficiency in digital and technological tools

Commitment to Diversity & Inclusion:

We are committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.