Key skills
Communication
About this role
Role Overview
- Receive study-specific requests and operational guidance from the Site Engagement Leads
- Serve as the “face” of the client to develop/strengthen relationships with new/current clinical trial investigators
- Maintain clear and consistent communication channels with site coordinators, investigators, and staff
- Develop tailored engagement plans and strategies for each investigator site
- Analyze patient enrolment and retention methods to identify potential roadblocks
- Monitor and manage clinical study sites, including initiation, routine visits, and closeout activities
- Support feasibility assessments, budget negotiations, and regulatory submissions
- Travel extensively (60–80%) to support site activities and maintain audit readiness.
Requirements
- Bachelor’s degree in life sciences or related field, or equivalent clinical research experience
- Minimum 5 years of site engagement and clinical monitoring experience in pharmaceutical or CRO setting
- Strong knowledge of regulatory requirements and drug development processes
- Advanced site monitoring and management skills
- Excellent communication, organizational, and problem-solving abilities
- Proficiency in relevant computer applications and systems
- Valid driver’s license and ability to travel extensively.
Benefits
- Paid time off
- Flexible working arrangements