Administration-Management Hospital Based job located in Florida

Job Summary
We are seeking a dynamic and detail-oriented Clinical Project Manager to lead and oversee the planning, execution, and completion of clinical trials. This pivotal role involves coordinating cross-functional teams, ensuring compliance with regulatory standards, and maintaining rigorous data collection processes. The ideal candidate will demonstrate exceptional leadership skills, a strong background in scientific research and clinical studies, and a passion for advancing healthcare through innovative research. Join us to drive impactful clinical projects that contribute to groundbreaking medical discoveries and improve patient outcomes worldwide.

Responsibilities

• Lead the development and management of clinical trial protocols, ensuring alignment with project goals and regulatory requirements.
• Oversee all aspects of clinical trial operations, including site selection, initiation, monitoring, and close-out activities.
• Supervise multidisciplinary teams, providing guidance and support to ensure timely delivery of project milestones.
• Ensure adherence to Good Clinical Practice (GCP) guidelines and ICH standards across all trial activities.
• Manage data collection processes, ensuring accuracy, completeness, and compliance with data management plans.
• Coordinate with laboratories and research sites to facilitate sample processing, testing, and reporting.
• Maintain comprehensive documentation for audits, inspections, and regulatory submissions while managing project timelines effectively.
• Ensure compliance with applicable regulations and company policies related to clinical research and project management.

Experience

• Proven supervising experience in clinical research or project management within a healthcare or scientific environment.
• Extensive background in scientific research, clinical trials, or laboratory work with a clear understanding of research methodologies.
• Demonstrated leadership in managing cross-functional teams across multiple projects or sites.
• Strong knowledge of data collection techniques, laboratory procedures, and regulatory standards such as GCP and ICH guidelines.
• Valid ICH GCP certification from a recognized issuer (e.g., CA or equivalent) is required.
• Experience in project management tools and compliance management practices to ensure smooth trial execution.
• Familiarity with clinical research software platforms and documentation best practices is highly desirable. Join us as a Clinical Project Manager to be at the forefront of medical innovation! Your expertise will help shape the future of healthcare by ensuring that our clinical trials are conducted efficiently, ethically, and successfully—making a real difference in patients’ lives around the globe.

Benefits:

• 401(k)
• Dental insurance
• Flexible schedule
• Health insurance
• Life insurance
• Paid time off
• Vision insurance