Clinical Trial Manager

About the role

For our client, we are seeking a Clinical Trial Manager to join the team of a leader in the Pharmaceuticals & Biotech space. This role will support clinical priorities focused on quality, patient-centered outcomes, and effective care delivery. You will collaborate with clinical leaders, operational teams, and cross-functional stakeholders to improve standards, workflows, and execution. The position offers the opportunity to strengthen care quality, team performance, and measurable outcomes within a life sciences environment.

Responsibilities

• Lead clinical study planning, execution, and oversight while ensuring regulatory compliance
• Partner with cross-functional teams to meet study objectives and timelines
• Manage CROs and vendors, including overseeing site payments and monitoring visits
• Track study timelines, enrollment, vendor performance, and financial metrics
• Identify risks and challenges early, implementing solutions for successful study outcomes
• Support contract negotiations and ensure study activities stay within scope and budget
• Facilitate study team meetings, providing updates on progress and milestones

Qualifications

• Bachelor's degree in a scientific, clinical, or health-related field; advanced degree preferred
• 8+ years in pharmaceutical, biotechnology, diagnostics, or CRO, with 5+ years as CRA/Senior CRA
• Global clinical study experience, especially in Europe and Asia-Pacific, preferred
• In-depth knowledge of GCP, ICH, FDA regulations, and global clinical research
• Experience in managing CROs, vendors, and study partners for project success
• Strong project management, organizational, and budgeting skills under tight deadlines
• Excellent communication, problem-solving, and analytical skills

Benefits

• Hybrid work model with in-person collaboration and work-from-home options
• Flexible work hours to enhance work-life balance
• Opportunities for professional development and continued education support