Note: The job is a remote job and is open to candidates in USA. Alimentiv is a company focused on clinical research, and they are seeking a Clinical Project Manager. The role involves managing clinical research projects, ensuring compliance with regulations, and acting as a liaison between clients and sponsors throughout the project lifecycle.
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
Skills
- Bachelor's Degree in a relevant field of study
- 1-3 years of experience in clinical study management
- Self-motivation with strong communication skills
- Commitment to achieving positive results
- Strong attention to detail
- 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
- Health Sciences, Clinical Research preferred
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