Clinical Project Coordinator providing administrative and clerical support for research projects. Coordinating trainings, meetings, and documentation management to ensure compliance with quality standards.
Responsibilities
Provide administrative, clerical, implementation and/or processing support to the project teams and stakeholders
Assist with document/process/report development, testing, tracking, distribution, and management
Coordinate meetings, presentations, and training activities
Facilitate billing and payment activities
Act as first point of contact for project queries
Ensure that all activities align with quality standards, project guidelines, corporate best practices, and regulatory standards and guidelines
Requirements
Applicants should have a minimum of one to three years of related work experience with ongoing training
a minimum of a one-year College Advance Diploma/Degree in a relevant field of study, preferable in Health or Life Sciences, or Clinical Research
Knowledge of clinical research
ability to work independently
strong communication skills
ability to work in a cross-functional environment
Benefits
*Accommodations for job applicants with disabilities are available upon request
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