Remote Global Clinical Operations Leader

Alimentiv; Washington (District of Columbia); On-site; USD 110,000 - 150,000; Full time

Benefits offered by this job

Bonus

Job summary

Alimentiv is seeking a capable Clinical Operations Lead to oversee a project at regional/global level. You will coordinate CRAs and investigator sites, ensure adherence to the Monitoring Plan, GCP, ICH, and local regulations, and serve as the primary liaison with the clinical project team.

You will develop study tools, supervise enrollment strategies, train CRAs, review site performance, and contribute to project planning and metrics while supporting other functions such as Data Management and

Qualifications

• College diploma/degree AND 7-9 years related experience +continuous training and knowledge/skills upgrading.
• Undergraduate university degree (Bachelors or Honors Bachelors) AND 4-6 years' experience + substantial on-going job-related training.
• Health Sciences, Life Sciences or Nursing specialty preferred, or SoCRA and/or ACRP Certification/Designation.
• Should have a minimum of 3 years CRA experience, strong experience with EDC systems, proficient with MS Office, strong written and verbal communication skills and interpersonal/organizational skills.

Responsibilities

• Oversee regional CRAs to ensure site compliance with study protocol, timelines and ICH-GCP.
• Provide monitoring support visits to aid site/CRA performance and compliance with standards.
• Review visit reports for quality and site management.
• Oversee startup and feasibility activities.
• Contribute to financial project management and vendor oversight as applicable.

Skills

MS Office

EDC systems

Written communication

Verbal communication

Interpersonal skills

Organizational skills

Education

College diploma/degree

Undergraduate university degree

Tools

EDC systems

MS Office

Job description

Alimentiv is seeking a capable Clinical Operations Lead to oversee a project at regional/global level. You will coordinate CRAs and investigator sites, ensure adherence to the Monitoring Plan, GCP, ICH, and local regulations, and serve as the primary liaison with the clinical project team.

You will develop study tools, supervise enrollment strategies, train CRAs, review site performance, and contribute to project planning and metrics while supporting other functions such as Data Management and