Alimentiv Hiring For Clinical Project Manager (Remote) at Toronto, ON Full Time

JOB INFORMATION

Job Title: Clinical Project Manager (Full-time, Permanent)

Location: Canada/US (Remote-based)

Reports To: Project Director

Department/Unit Name: Clinical Services > Clinical Study Management

This is an exciting opportunity to join a niche GI CRO and recognized expert in IBD and Clinical Trial Design. Alimentiv is a culturally diverse organization that is committed to fostering a positive, healthy, and peaceful work environment where kindness and collaboration are a commonplace. The mission of transforming human health is our purpose and a defining pillar of the culture. You will experience the solidarity, drive, and satisfaction of contributing to this purpose. Your work will be meaningful and appreciated by your colleagues, the community, and society at large.

As a private, for-profit, and social enterprise, we have different objectives than traditionally structured companies. We can offer a different kind of employee experience: competitive and innovative with value placed on social improvement and recognizing employees for the roles they play in the growth of the organization.

We are looking for an extraordinary Clinical Project Manager to join our global talented and collaborative Full Service Clinical Project Management Team.

JOB SUMMARY:

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, he or she 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 be managing the day to day activities and performance of a multidisciplinary project team, ensuring all decisions align with corporate, industry, sponsor and regulatory requirements.

GENERAL AREAS OF RESPONSIBILITY:

Project Management

• 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.

Documents and Tools

• 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.

Project Team Performance

• 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.

Client/Sponsor Support

• 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.

QUALIFICATIONS:

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 team work.

WORKING CONDITIONS:

Home Based

Occasional travel

• Accommodations for job applicants with disabilities are available upon request

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