FSP CTM / Sr. CTM

📋 Description

• Lead clinical trial operations for studies of low to moderate complexity
• Oversee timelines, quality, costs, and contractual commitments
• Collaborate with clinical teams, project managers, and study sites
• Contribute to study start-up, monitoring strategy, risk management, and process improvement
• Provide strong judgment and communication in complex clinical situations
• Remote opportunity for an experienced clinical professional

🎯 Requirements

• Bachelor’s degree or equivalent qualification
• At least 5 years in clinical research/monitoring/CRTM or related field
• Oncology trial experience highly preferred
• Strong understanding of ICH-GCP, FDA guidelines, and relevant regulations
• Proven leadership, mentoring, and cross-functional collaboration skills
• Excellent planning, organization, and communication in multicultural/matrix settings

🎁 Benefits

• Fully remote work opportunity
• Full-time with standard Monday–Friday schedule
• Global clinical research program exposure and meaningful impact
• Opportunities to work with multidisciplinary teams in an international environment
• Professional development through leadership, mentoring, and collaboration
• Chance to work with complex clinical studies and develop trial management expertise