Remote Clinical Study Manager for AI Training (Contract)

Alignerr Corp.; Denver (CO); Remote; USD 83,000 - 165,000; Part time

Job summary

Alignerr is seeking an experienced Clinical Study Manager to oversee operational execution of clinical trials and contribute to AI training workflows informed by real-world healthcare data. This is a fully remote, hourly contract role built for experienced clinical research professionals who want meaningful, high-impact work on their own schedule, with 10–40 hours per week.

Ideal candidates bring a strong track record in budgets, timelines, and vendor relationships, and excel in remote,

Qualifications

• Experience managing budgets, timelines, and vendor relationships in clinical trials.
• Proven ability to coordinate CROs, sites, and cross-functional teams in complex environments.
• Highly organized, detail-oriented, and able to navigate ambiguity in fast-moving research settings.
• Strong communication skills to keep stakeholders aligned while maintaining quality.
• Ability to work independently in a remote, asynchronous environment.

Responsibilities

• Manage clinical trial timelines, milestones, and deliverables to keep studies on track and on budget.
• Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and partners.
• Coordinate with CROs, investigator sites, and internal teams to ensure smooth, high-quality study execution.
• Identify operational risks early, resolve issues decisively, and keep all stakeholders aligned throughout the trial lifecycle.
• Apply your clinical expertise to evaluate and inform AI training workflows grounded in real clinical research processes.

Skills

Clinical trial management

Budget & forecasting

Vendor management

Cross-functional coordination

Remote work communication

Documentation & reporting

Job description

Alignerr is seeking an experienced Clinical Study Manager to oversee operational execution of clinical trials and contribute to AI training workflows informed by real-world healthcare data. This is a fully remote, hourly contract role built for experienced clinical research professionals who want meaningful, high-impact work on their own schedule, with 10–40 hours per week.

Ideal candidates bring a strong track record in budgets, timelines, and vendor relationships, and excel in remote,