Global Clinical Monitoring & Site Management Lead

Alimentiv; Minneapolis (MN); Remote; USD 111,000 - 174,000; Full time

Benefits offered by this job

Education reimbursement

Cell phone allowance

Remote work allowance

Office setup allowance

Mentorship program

Job summary

Alimentiv is a global CRO focused on GI therapies, seeking a Manager to lead Clinical Monitoring, overseeing teams, regulatory compliance, and project delivery. The role requires coordinating with sponsors and sites to maintain quality and timeliness across the lifecycle.

The position emphasizes staff development, process improvement, and collaboration across time zones, with remote/global work and a competitive benefits package.

Qualifications

• College diploma or university degree in a relevant field, preferably Health Sciences or Life Sciences; SoCRA and/or ACRP certification/designation is considered an asset.
• Minimum 4–6 years of relevant clinical research/clinical monitoring experience with substantial ongoing training.
• Demonstrated experience managing CRA or Clinical Monitoring staff, including performance management, resource planning and staff development.
• Proven ability to train, mentor and support colleagues in both one-to-one and team settings.
• Strong knowledge of ICH‑GCP, applicable clinical research regulations and guidelines, and clinical monitoring best practices.
• Demonstrated leadership skills with the ability to engage, develop and support high‑performing teams.
• Strong stakeholder management skills and a collaborative, customer‑focused and solution‑oriented approach.
• Strong verbal and written communication skills, with the ability to work effectively with internal teams, sponsors and external partners.
• Excellent organisational and prioritisation skills, with the ability to manage multiple responsibilities and deadlines in a dynamic environment.
• Ability to work effectively in a remote, global environment and collaborate across functions, geographies and time zones.

Responsibilities

• Lead the day‑to‑day delivery of the Clinical Monitoring function, ensuring high-quality, timely and compliant services across assigned projects.
• Manage and develop Clinical Operations Leads, including resource planning, work allocation, training and development, employee engagement and performance management.
• Ensure appropriate staffing levels across projects, balancing operational requirements, team capacity and project priorities.
• Partner with clinical monitoring and project leadership to develop and oversee project‑specific strategies and processes relating to site selection, monitoring, ICH‑GCP compliance and global project delivery.
• Provide oversight and support for the identification, escalation and resolution of site, sponsor and clinical monitoring issues.
• Drive the development and continuous improvement of policies, procedures, tools and processes supporting Clinical Monitoring activities.
• Partner with internal stakeholders, sponsors and research sites to identify opportunities for improvement and support the implementation of new technologies and processes.
• Identify, engage and manage independent contractor resources, including recruitment, contract support, training, cost monitoring, compliance and performance management.
• Ensure Clinical Monitoring activities comply with applicable regulations, ICH‑GCP, organizational procedures and industry best practices.
• Provide Clinical Monitoring expertise to project teams and Business Development throughout the project lifecycle, from the bidding process through project delivery and reporting to sponsors.

Skills

Clinical monitoring experience

Staff management

Regulatory knowledge

ICH-GCP knowledge

Stakeholder management

Communication skills

Leadership

Organisational skills

Remote collaboration

Education

Health Sciences degree

Job description

Alimentiv is a global CRO focused on GI therapies, seeking a Manager to lead Clinical Monitoring, overseeing teams, regulatory compliance, and project delivery. The role requires coordinating with sponsors and sites to maintain quality and timeliness across the lifecycle.

The position emphasizes staff development, process improvement, and collaboration across time zones, with remote/global work and a competitive benefits package.