Clinical Project Manager (US)

About the Role

The Clinical Project Manager role is essential to the success of Alimentiv's clinical research initiatives. You will be responsible for developing and implementing project plans, ensuring that projects are completed on time, within budget, and to the required quality standards. Your ability to build and maintain strong relationships with stakeholders, including investigators, sponsors, and team members, will be crucial to the success of the projects.

You will be part of a dynamic team that values innovation, collaboration, and continuous learning. Alimentiv is committed to providing a supportive and inclusive work environment that fosters growth and development.

What You Will Do

• Manage the planning, execution, and completion of clinical research projects
• Ensure compliance with applicable regulations, guidelines, and corporate policies
• Develop and implement project plans, resource allocation plans, and other project-related documents
• Coordinate and facilitate project meetings, including investigator meetings and sponsor meetings
• Maintain accurate and up-to-date project records and documentation
• Develop and manage project budgets, track expenses, and ensure timely payment to vendors
• Identify, assign, and monitor the completion of interdisciplinary project tasks
• Ensure task completion performance meets or exceeds quality standards and sponsor/client expectations
• Act as primary liaison with clients/sponsors throughout the project life cycle
• Develop and deliver project status reports, presentations, and other project-related communications

What We Are Looking For

• Bachelor's Degree in a relevant field of study (Health Sciences, Clinical Research preferred)
• 1-3 years of experience in clinical study management
• Strong communication and project management skills
• Ability to work independently and as part of a cross-functional team
• Strong attention to detail and ability to prioritize tasks
• Ability to engage in continuous learning and self-development
• Ability to foster teamwork and collaborate with stakeholders
• Fluent in reading, writing, and speaking English

Nice to Have

• Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS)
• Knowledge of Good Clinical Practice (GCP) and regulatory requirements
• Certification in clinical research or project management (e.g., CCRA, CCRP, PMP)
• Experience with budgeting and financial management

Benefits and Perks

• Competitive salary and benefits package
• Opportunity to work remotely and flexible working hours
• Professional development and training opportunities
• Collaborative and supportive work environment
• Access to cutting-edge technology and tools
• Recognition and reward for outstanding performance
• Comprehensive health insurance and retirement plan
• Paid time off and holidays
• Remote work stipend and home office setup support

• Develop a strong understanding of clinical research regulations and guidelines, such as GCP and ICH-GCP, to stand out as a candidate.
• Create a portfolio that showcases your project management skills, including examples of successful project plans, budgets, and timelines.
• Highlight your ability to work independently and as part of a cross-functional team, as well as your excellent communication and interpersonal skills.
• Be prepared to discuss your experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) during the interview process.
• Research Alimentiv's company culture and values to demonstrate your enthusiasm for the role and the company, and to show that you are a strong fit for the team.
• Be prepared to negotiate your salary and benefits package, and to discuss your long-term career goals and how they align with the company's vision.