We bring you a modern, fast, and transparent approach to your trial operations. You deserve excellence without excuses.

Contact Info
East Brunswick, New Jersey, USA 08816 atahir@sunclinicaltrials.com

Services

Our Services

Inside the Workflow of our Clinical Trials.

At Sun Clinical Trials, we specialize in managing global clinical trials for neurodegenerative and neuropsychiatric disorders across all phases: start-up, maintenance, and close out. Our team brings deep expertise in the operational complexities of neuroscience studies, including Alzheimer’s, Parkinson’s, multiple sclerosis, depression, and schizophrenia. We ensure rigorous site selection, timeline adherence, risk mitigation, and data integrity to support high quality outcomes in even the most challenging trial landscapes. With a focus on patient centric solutions and regulatory compliance, we help sponsors advance neuroscience breakthroughs with efficiency and confidence.

Our services cover every operational layer of clinical trial execution, with a focus on precision, transparency, and science driven oversight:

Study Start-Up

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Streamlined Start-Up & Vendor Oversight Data-driven site selection, regulatory submissions, vendor coordination, and global contract/budget management.

  • Feasibility & Site Selection: Using data-driven tools and historical enrollment performance to identify the most suitable sites across global regions.
  • Regulatory Submissions & CTA Management: Coordinating EU CTR submissions, managing country-specific requirements, and supporting HA and EC approvals.
  • Vendor Engagement: Leading vendor selection, scope definition, and kick-off (e.g., central labs, eCOA, imaging, IRT).
  • Site Contracts & Budgets: Overseeing contract negotiation strategies and budget alignment across varied regions (EU, US, APAC, LATAM).

Maintenance Phase

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Proactive Trial Oversight & Patient Engagement Risk-based study monitoring, vendor governance, global communication coordination, and tailored recruitment strategies for high-performing trials.

  • Study Oversight: Providing structured oversight through risk-based monitoring plans, enrollment tracking, deviation trend reviews, and issue management dashboards.
  • Vendor Oversight: Leading regular governance meetings with key vendors to ensure timelines, deliverables, and KPIs are met.
  • Patient Engagement: Supporting country and site-level tactics to boost recruitment and retention, especially in challenging CNS populations.
  • Communication Management: Acting as the central communication hub between sponsors, CROs, and sites, driving collaboration across time zones.

Close Out

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Seamless Close-Out & Inspection Readiness Coordinated database lock, site close-out execution, and TMF management to ensure compliance and audit preparedness.

  • Database Lock Coordination: Aligning all operational stakeholders to meet clean file and lock timelines.
  • Site Close-Out Visits & Documentation: Ensuring close-out packages are completed per SOPs and regulatory requirements.
  • Trial Master File (TMF) Oversight: Managing TMF health, QC cycles, and inspection readiness throughout the study.

Full Support

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At Sun Clinical Laboratories, our Full Support service is designed to guide you through every phase of the clinical trial process. From initial planning and protocol development to patient recruitment, data management, and final reporting, we provide seamless integration of services to ensure your trial's success.

  • Complete trial support from start to finish
  • All services integrated for smooth execution
  • Customized plans to fit your study goals
  • Expert team you can trust