UniTriTeam

Clinical Research

• Conduct outbound and inbound phone calls with prospective study participants
• Respond promptly to web inquiries, referrals, and marketing-generated leads
• Perform detailed prescreening interviews using approved study criteria
• Educate potential participants on clinical research and study expectations
• Build rapport and establish trust with individuals seeking treatment options
• Schedule qualified participants for screening visits with the research site
• Document all patient interactions accurately within the site's recruitment systems and CTMS/CRM
• Maintain consistent follow-up with interested participants until disposition
• Ensure all patient communications comply with sponsor, IRB, HIPAA, and site requirements
• Collaborate closely with Clinical Research Coordinators and site staff regarding scheduling and participant status
• Maintain daily productivity and quality metrics
• Participate in team meetings, coaching sessions, and ongoing training
• Identify opportunities to improve recruitment conversion rates and patient experience
• Handle 60+ outbound/inbound patient calls per day
• Schedule 8–10 qualified patient appointments per week
• Complete timely follow-up on all assigned leads
• Complete accurate documentation the same day
• Deliver high patient satisfaction through compassionate communication
• Maintain strong attendance and schedule adherence
• Contribute to enrollment goals through productivity, quality, conversion rates, scheduling success, and documentation accuracy

Explore Patient Recruitment Specialist – CNS Clinical Research at UniTriTeam. Review requirements and application details.

Patient Recruitment Specialist – CNS Clinical Research

Recruitment

• Conduct outreach to potential clinical trial participants via inbound and outbound calls
• Pre-screen and assess patients for eligibility based on study protocols
• Educate patients on clinical trial participation, benefits, and expectations
• Maintain accurate interaction records in the recruitment tracking system
• Collaborate with study teams to ensure timely follow-up and enrollment
• Use CRM software such as HubSpot and phone systems for communication and tracking
• Provide culturally sensitive support in English and Spanish as needed
• Target 70 calls per day and schedule 5 patients per day for screening visits

Explore Patient Recruiter at UniTriTeam. Review requirements and application details.

Patient Recruiter

Frontend Engineer

• Design, build and maintain scalable web applications, front-end and back-end
• Translate wireframes, mockups and functional specs into high-quality code
• Build responsive, modern UIs using React, TypeScript and Tailwind CSS
• Develop back-end services and RESTful APIs using Node.js and Express
• Work with PostgreSQL and NoSQL databases, including schema design and query development
• Integrate third-party services and APIs, such as Stripe, OpenAI and authentication providers
• Implement background job processing using BullMQ/Redis and handle CSV and Excel data imports/exports
• Optimize applications for speed, scalability and performance
• Implement testing, CI/CD workflows and version control best practices
• Troubleshoot and debug across the full stack and external services
• Maintain clear documentation to support future scaling
• Collaborate with product and engineering teams and iterate on customer feedback

Explore Full Stack Web Developer – PST/EST/CST Timezone at UniTriTeam. Review requirements and application details.

Full Stack Web Developer – PST/EST/CST Timezone

• Own and manage the study start-up process from initial study award or feasibility through site activation and readiness for first patient enrollment.
• Develop study start-up plans, timelines, milestones, and deliverables.
• Coordinate regulatory, contracts, budgets, clinical operations, finance, recruitment, technology, and other functional teams.
• Track feasibility, regulatory submissions, IRB approvals, contracts, budgets, training, system readiness, and sponsor requirements.
• Ensure study documentation, approvals, and operational requirements are complete before site activation.
• Identify critical-path activities, dependencies, delays, and mitigation plans.
• Serve as the central coordination point for internal departments, sponsors, CROs, vendors, and site leadership.
• Lead start-up meetings, assign action-item owners, and drive follow-through.
• Escalate risks, delays, and unresolved issues with recommended solutions and recovery plans.
• Build and maintain project plans, study start-up trackers, milestone reports, and centralized documentation.
• Coordinate operational readiness, including staffing, training, supplies, systems, and required documentation.
• Verify readiness of CTMS, eRegulatory, eSource, EDC, and other study-specific systems.
• Ensure compliance with GCP, regulatory requirements, sponsor expectations, and organizational SOPs.
• Support handoffs from study start-up to ongoing clinical research operations.
• Provide structured status updates on study progress, milestones, risks, and next steps.
• Facilitate meetings with documented decisions, owners, and due dates.
• Drive accountability, remove bottlenecks, and improve study start-up workflows and activation cycle times.

Explore Clinical Research Project Manager – PST/EST/CST Timezone at UniTriTeam. Review requirements and application details.

Open roles

Patient Recruitment Specialist – CNS Clinical Research

Patient Recruiter

Full Stack Web Developer – PST/EST/CST Timezone

Clinical Research Project Manager – PST/EST/CST Timezone