Alimentiv is seeking a dedicated Study Start Up Specialist to join our team in a fully remote capacity. In this role, you will play a pivotal part in the clinical trial process by managing site-related start-up activities and serving as the primary point of contact for study sites, ensuring seamless communication and project progression.
Key responsibilities
- Create and distribute study-specific start-up document packages while ensuring all returned documents meet internal quality and regulatory standards.
- Act as the main liaison for sites during contract and budget negotiations, working closely with legal and project management teams.
- Maintain accurate site intelligence trackers, including timelines, recruitment data, and negotiation progress.
- Develop and nurture professional relationships with study personnel to facilitate the timely completion of all start-up milestones.
- Track project progress using designated systems and provide regular reports on metrics and site readiness.
Requirements
- Undergraduate degree or college diploma with relevant experience in clinical study site operations.
- Fluency in both English and French is essential for this position.
- Strong understanding of clinical site start-up requirements and regulatory documentation.
- Excellent communication skills with the ability to manage complex interactions with various stakeholders.
- Proven ability to work independently, set personal pace, and manage multiple tasks with a high sense of urgency.
What we offer
- The opportunity to work in a fully remote environment within a global clinical research organization.
- Professional growth and the chance to contribute to impactful clinical studies.
- A collaborative team culture that values expertise and proactive problem-solving.