Clinical Project Manager

September 20

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Logo of Alimentiv

Alimentiv

Clinical Trials Design • Planning • Safety Management • Custom Services • Study Management

Description

• 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.

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

Benefits

• Home Based • Occasional travel

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