Offer summary

Qualifications:

Minimum of one to three years of related work experience., A three-year College Advance Diploma or Degree in a relevant field, preferably in Health Sciences or Clinical Research., Strong communication skills and self-motivation., Attention to detail and ability to build collaborative relationships..

Key responsibilities:

Manage planning, execution, and completion of clinical research projects.

Ensure compliance with regulations, guidelines, and policies.

Coordinate data, documents, and project tools throughout the project lifecycle.

Act as primary liaison with clients and sponsors, providing updates and resolving issues.

Job description

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 adaptdevelop, implement, monitor and be accountable for project protocols, operational plans, risk management, resources, project toolsmaterials, 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.

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 andor participate in the development of project communications, training, regulatory submissions andor audits and selection of third party vendors as required.

Documents and Tools
Manage a crossfunctional 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 safetyadverse event management, document management, statistical analysis andor final report writing and publications.
Ensure task completion performance meets or exceeds quality standards and sponsorclient, project and regulatory expectations and guidelines.

ClientSponsor Support
Act as primary liaison throughout the project life cycle ensuring clientsponsor expectations are appropriately managed by addressing and resolving queriesissues, 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 sponsorclient 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 threeyear College Advance DiplomaDegree in a relevant field of study, preferable in (Health) Sciences or Clinical Research.
The successful candidate must exhibit the following skills: selfmotivation 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 selfdevelopment.
Ability to continually foster teamwork.

Working Conditions
Home Based
Occasional travel
*Accommodations for job applicants with disabilities are available upon request
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