Responsibilities

• Organize and participate in Monitor's and Investigator's Meetings to ensure effective communication and project alignment.
• Conduct co-monitoring visits for assigned clinical projects, ensuring adherence to study protocols and compliance regulations.
• Oversee the execution and delivery of clinical studies, ensuring all phases are completed on time and within budget.
• Manage vendor, site, and CRO activities, ensuring high-quality data collection and reporting.
• Track study progress, addressing any issues or delays as they arise, and implement solutions proactively.
• Collaborate closely with cross-functional teams to facilitate project success and maintain strong client relationships.
• Provide mentorship and training to junior team members to foster a supportive and growth-oriented environment.

Requirements

• Bachelor's degree in a relevant field; advanced degree preferred.
• A minimum of 5 years of experience in clinical project management, specifically within a Clinical Research Organization (CRO).
• Strong background in managing complex oncology and hematology clinical trials.
• Proven ability to work independently and manage multiple projects simultaneously in a fast-paced environment.
• Excellent communication skills, both verbal and written, with a focus on building relationships and teamwork.
• Knowledge of regulatory requirements and Good Clinical Practice (GCP).
• Willingness to travel for monitoring visits and client meetings as needed.

Benefits

• Competitive salary and performance-based bonuses.
• Flexible working arrangements, including remote work options.
• Comprehensive health, dental, and vision insurance plans.
• Generous paid time off and holiday policies.
• Opportunities for professional development and career advancement.
• A supportive and inclusive company culture that promotes work-life balance.