Clinical Operations Project Manager
By Intelliswift Software At Upper Gwynedd, PA, United States
• Education Requirement: BA/BS/Masters in a scientific or technological field of study.
• Minimum experience requirement: 2-3years of experience with clinical trial set-up and execution.
Job Title: Clinical operation project manager (Project Manager Scientific I (Assistant)
Software: MS office suite, any document review software experience is good to have.
• Clinical study operation experience.
Location: Upper Gwynedd, PA or WestPoint PA or Rahway, NJ

Are you looking for an exciting opportunity to join a dynamic team and make a real impact? We are looking for a Project Coordinator with Clinical Operations experience to join our team and help us drive our clinical operations forward. You will be responsible for coordinating and managing clinical operations projects, ensuring that all project timelines and deliverables are met. If you have a passion for clinical operations and are looking for a challenging and rewarding role, then this is the perfect opportunity for you!

Overview Project Coordinators with Clinical Operations are responsible for providing administrative and operational support to clinical research projects. They coordinate the activities of the project team, manage timelines, and ensure that the project is completed on time and within budget. Detailed Job Description Project Coordinators with Clinical Operations are responsible for providing administrative and operational support to clinical research projects. They coordinate the activities of the project team, manage timelines, and ensure that the project is completed on time and within budget. They are also responsible for tracking project progress, preparing reports, and communicating with stakeholders. Project Coordinators with Clinical Operations must have excellent organizational and communication skills, as well as the ability to work independently and as part of a team. They must be able to manage multiple tasks and prioritize work to meet deadlines. Job Skills Required
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize work to meet deadlines
• Knowledge of clinical research processes and regulations
• Proficiency in Microsoft Office Suite
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research or project management
• Knowledge of clinical research processes and regulations
• Proficiency in Microsoft Office Suite
Job Knowledge
• Knowledge of clinical research processes and regulations
• Knowledge of project management principles and techniques
• Knowledge of data analysis and reporting
Job Experience
• At least two years of experience in clinical research or project management
• Experience in coordinating and managing clinical research projects
• Experience in preparing reports and presentations
Job Responsibilities
• Coordinate and manage clinical research projects
• Track project progress and prepare reports
• Communicate with stakeholders and ensure project deadlines are met
• Monitor project budget and ensure that project is completed within budget
• Prepare presentations and other materials for project meetings
• Ensure compliance with clinical research regulations and guidelines