Our Capabilities

Sunrise Medical and Research is fully equipped to manage clinical trials from start to finish, with expertise across diverse therapeutic areas and Phases II-IV. Our capabilities include participant recruitment, data management, regulatory compliance, and investigational product handling, all executed with precision and efficiency. By combining advanced technology with a highly skilled team, we ensure that every trial is conducted to the highest standards, delivering reliable data and maintaining participant safety. Whether you're looking to conduct a trial in a specialized medical field or across multiple phases, we are a trusted partner for Sponsors seeking excellence in clinical research.

Our Facility

Exam Rooms

Our facility houses multiple private and fully-equipped exam rooms designed to provide a comfortable and secure environment for study participants. Each room is furnished with modern medical equipment, ensuring accurate assessments and monitoring throughout the clinical trial. Privacy and patient comfort are our top priorities, with soundproofing and adjustable lighting to cater to each participant’s needs. The layout allows for seamless coordination between healthcare professionals, ensuring efficient and timely examinations.

Laboratory

The laboratory at Sunrise Medical and Research is a cutting-edge facility equipped with advanced diagnostic tools and technology. It allows for timely and precise processing of biological samples, ensuring high-quality data collection. The lab operates under strict compliance with GCP and CLIA regulations, with regular calibration and maintenance of equipment to guarantee accuracy. Our experienced laboratory technicians work closely with clinical teams to ensure seamless integration of lab results into the clinical trial process.

Pharmacy

Our on-site pharmacy is a controlled and secure environment that adheres to stringent regulatory standards for the storage, handling, and dispensing of investigational products (IP). The pharmacy is equipped with temperature-controlled storage units, including refrigerators and freezers, monitored 24/7 for any fluctuations. Our experienced pharmacy staff is trained in Good Clinical Practice (GCP) and follows rigorous protocols to ensure accurate dispensing and accountability of IPs, with detailed records maintained for audit readiness.

Document Storage

Our document storage space is a dedicated, secure area designed to meet the highest standards of confidentiality and compliance. All study-related documents, including informed consent forms, case report forms, and regulatory documents, are stored in a secure, access-controlled environment. We utilize both physical and electronic storage solutions. This ensures that all documents are easily accessible for audits and inspections, while also maintaining data integrity and security.

Our facility is a reflection of our commitment to excellence in clinical research. By maintaining the highest standards in our exam rooms, pharmacy, laboratory, and document storage space, Sunrise Medical and Research ensures that every aspect of your clinical trial is managed with precision, care, and compliance. We welcome Sponsors to visit our site and experience firsthand the quality and dedication we bring to every study.

Our Staff

Investigators

Our Principal Investigators are seasoned medical professionals with extensive experience in clinical research across various therapeutic areas. They are responsible for the overall conduct of the study, ensuring that all trials are scientifically sound, ethically conducted, and compliant with regulatory requirements. Their leadership is crucial in maintaining the integrity of the research and safeguarding participant welfare.

Coordinators

Our Clinical Research Coordinators are the backbone of our trial operations. They manage the day-to-day activities of the studies, including participant recruitment, informed consent, scheduling, and data collection. With a keen attention to detail and strong organizational skills, our CRCs ensure that each trial is executed efficiently and in strict adherence to the protocol, while also serving as the main point of contact for participants and Sponsors.

Regulatory Specialist

The Regulatory Affairs Team at Sunrise Medical and Research is tasked with ensuring that all studies comply with local, national, and international regulations. This team manages the preparation and submission of regulatory documents, oversees the maintenance of trial master files, and ensures that our site is always audit-ready. Their work is essential in maintaining the legal and ethical integrity of our research.

Pharmacy Staff

The Pharmacy Team at Sunrise Medical and Research is responsible for the secure handling, preparation, and dispensing of investigational products (IP). Our pharmacists and pharmacy technicians are trained in Good Clinical Practice (GCP) and adhere to rigorous protocols to ensure the integrity and accurate dosing of all medications. Their expertise ensures that all IPs are managed according to the highest standards of safety and compliance.

The team at Sunrise Medical and Research is unified by a common goal: to advance medical science through high-quality clinical trials while ensuring the best possible experience for our participants. Our collective expertise, dedication, and adherence to the highest standards set us apart in the field of clinical research.