Clinical Project Manager

September 20

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

201 - 500

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 • 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 • 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

Requirements

• Applicants should have a minimum of one to three years of related work experience with ongoing training • 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