Clinical Project Manager

September 20, 2024

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Logo of Alimentiv

Alimentiv

Alimentiv is a specialty contract research organization focused on gastrointestinal (GI) and liver diseases. With over 30 years of experience, Alimentiv offers a comprehensive range of clinical research and imaging services, including clinical trial management, site management, regulatory affairs, and precision medicine. The company is at the forefront of medical research and development, providing state-of-the-art imaging solutions and actionable biomarker insights. Alimentiv supports the development of GI compounds and is active in more than 60 countries, working with a network of medical and operational experts to accelerate clinical trials and patient recruitment.

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. • 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. • 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. • 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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