As the primary sponsor liaison and advocate, the Clinical Project Manager will plan, execute, manage, and monitor regional, single modality, or therapeutic area clinical research projects. Utilizing existing templates, processes, and programs as a guide, they will adapt/develop, implement, monitor, and be accountable for project protocols, operational plans, risk management, resources, project tools/materials, documents, and timelines. The successful candidate will manage the day-to-day activities and performance of a multidisciplinary project team, ensuring all decisions align with corporate, industry, sponsor, and regulatory requirements.Project ManagementManage the planning, execution, progress, and completion of assigned clinical research projects.Collaborate 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, audits, and the selection of third-party vendors as required.Documents and ToolsManage 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 to support proper conduct and execution throughout the project lifecycle.Project Team PerformanceIdentify, assign, and monitor the completion of interdisciplinary project tasks, including site monitoring, CRF and database development and revision, data collection, patient safety/adverse event management, document management, statistical analysis, and final report writing and publications.Ensure task completion performance meets or exceeds quality standards and sponsor/client, project, and regulatory expectations and guidelines.Client/Sponsor SupportAct as the primary liaison throughout the project lifecycle, managing client/sponsor expectations by addressing and resolving queries/issues, planning and executing project meetings, assisting with site and patient recruitment strategies and materials, developing stakeholder training, and providing regular project status and update reports.QualificationsApplicants should have a minimum of one to three years of related work experience with ongoing training, and a three-year College Advanced Diploma/Degree in a relevant field of study, preferably in (Health) Sciences or Clinical Research.The successful candidate must possess: self-motivation, strong communication skills, and a commitment to achieving positive results.Strong attention to detail and an understanding of the importance of building collaborative relationships to achieve results.Ability to engage in continuous learning and self-development.Ability to foster teamwork continually.Fluency in reading, writing, and speaking English.Working ConditionsHome-based environmentOccasional travelPHISHING SCAM WARNING: Alimentiv is aware of the increase in phishing scams via email, text, voice, and social media. Please note that Alimentiv only uses company email addresses containing "@alimentiv.com" for communication. If contacted about a job at Alimentiv, verify the sender's email domain and ensure they ask you to apply through this website. If you believe you've been a victim of a phishing scam, contact your local cyber authorities.#J-18808-Ljbffr