Sr. Clinical Research Associate
Job Summary
Job Description
Alimentiv is seeking a Sr. Clinical Research Associate to manage full clinical site monitoring services across one or more complex projects. This home-based role involves oversight of project monitoring, site recruitment, investigational site operations, and collaboration with sponsors and internal project teams.
Responsibilities:
- Act as primary liaison between clinical sites, CRAs, and project teams, ensuring compliance with study protocols and SOPs.
- Manage and deliver monitoring services, including site visits, patient recruitment, training, data/document management, and regulatory filings.
- Mentor, coach, and provide feedback to CRAs; assist in hiring, training, and supervision.
- Oversee monitoring reports, approve deliverables, and escalate issues to management as needed.
- Identify, recruit, and support site investigators, coordinating materials, protocols, and investigational products.
- Facilitate site access to study systems and ensure training and compliance requirements are met.
- Maintain collaborative relationships with stakeholders and provide ongoing updates and feedback.
Requirements:
- College diploma/degree with 4-6 years of related clinical research experience.
- Strong communication skills, self-motivation, attention to detail, and critical thinking abilities.
- Ability to travel regularly to investigational sites.
- Familiarity with GCP guidelines, SOPs, and clinical site operations.
- Capacity to manage multiple projects and resolve site or patient issues effectively.
Benefits:
- Opportunity to work on multinational, complex clinical trials.
- Home-based position with regular travel to sites.
- Exposure to clinical research project leadership and mentoring.
This role provides the opportunity to contribute to high-quality clinical research while ensuring adherence to regulatory standards and operational excellence.
