Clinical Project Manager

Summary

Join Alimentiv as a Clinical Project Manager and act as the primary sponsor liaison, planning, executing, managing, and monitoring clinical research projects. You will adapt and implement project protocols, manage project resources, and ensure compliance with regulations. The role involves managing a multidisciplinary team, overseeing project activities, and maintaining operational and regulatory integrity. Responsibilities include managing project documents and tools, ensuring team performance meets quality standards, and acting as the primary liaison with clients/sponsors. You will prepare reports, address client queries, and assist with recruitment strategies. The position is home-based with occasional travel.

Requirements

• Applicants should have a minimum of one to three years of related work experience with ongoing training, and a three-year College Advance Diploma/Degree in a relevant field of study, preferable in (Health) Sciences or Clinical Research
• The successful candidate must exhibit the following skills: self-motivation with strong communication skills and a commitment to achieving positive results
• Strong attention to detail and keenness to understand the importance of building collaborative relationships to achieve results
• Ability to engage in continuous learning and self-development
• Ability to continually foster teamwork
• Fluent in reading, writing, and speaking of English

Responsibilities

• Manage the planning, execution, progress and completion of assigned clinical research projects
• Work with functional experts to ensure all project activities comply with applicable regulations, guidelines, and corporate policies
• Maintain operational, financial and regulatory integrity and safety
• Develop and/or participate in the development of project communications, training, regulatory submissions and/or audits and selection of third party vendors as required
• Manage a cross-functional team to ensure the appropriate creation, delivery, maintenance and disposal of all related data, documents, equipment and tools, including protocols, SOPs, informed consent forms, case report forms and instructions
• Prepare investigator updates and other project related reports as required to support the proper conduct and execution throughout the life cycle of assigned projects
• Identify, assign and monitor the completion of interdisciplinary project tasks that include site monitoring, CRF and database development and revision, data collection, patient safety/adverse event management, document management, statistical analysis and/or final report writing and publications
• Ensure task completion performance meets or exceeds quality standards and sponsor/client, project and regulatory expectations and guidelines
• Act as primary liaison throughout the project life cycle ensuring client/sponsor expectations are appropriately managed by addressing and resolving queries/issues, planning and executing all project meetings, assisting with site and patient recruitment strategies and materials, assisting with the development of stakeholder training and by regularly providing sponsor/client with project status and update reports

Benefits

• Home Based
• Occasional travel