Clinical Project Manager I/II

Symbio is a contract research organization supporting global clinical studies across multiple therapeutic areas and medical devices. The Clinical Project Manager I/II will manage clinical trial projects from start-up through closeout, serving as the primary liaison among sponsors, internal teams, and vendors while ensuring delivery against timelines, budget, scope, and regulatory requirements.

Responsibilities:

• Lead planning and execution of clinical trial projects from proposal through closeout
• Act as primary sponsor liaison, ensuring alignment on scope, timelines, and deliverables
• Develop and maintain project management and study plans
• Coordinate cross-functional teams, vendors, and study stakeholders
• Support protocol development, study documentation, and regulatory deliverables
• Participate in feasibility, site selection, and bid defense activities
• Oversee training plans and study team readiness

Requirements:

• Bachelor's degree in Business Administration, Science, or related field (or equivalent experience)
• 3+ years in pharmaceutical and/or clinical research industry
• 1+ years in clinical project management
• Demonstrated experience in managing low to moderate complexity trials
• Strong knowledge of GCP, ICH guidelines, and clinical trial regulations
• Excellent communication, time-management, and organization skills
• Ability to manage multiple priorities in a fast-paced environment
• Proficiency in Microsoft Office