GreenLight Clinical has extensive experience in preclinical and clinical trial management demonstrated through numerous successful trials and long-standing relationships with our clients.
Our “people first” and patient centric approach underpins our practical management processes. Leveraging our own Central Laboratory we are able to manage the needs of patients and clients via on-site monitoring, and remote monitoring combined with careful management of targeted source data verification. Our highly qualified data teams are equipped with the experience and the technology to ensure accurate, robust and globally compliant trial reporting.
Embedded monitoring and management capability is underpinned by a commitment to patient safety, data integrity, risk assessment, and mitigation.
We focus on global consistency, transparency, support, and partnerships. This quality-driven approach is supported by our investment in class-leading software platforms including Medidata CTMS, Medidata Rave EDC, Viedoc, Veeva Vault, ArisGlobal and SAS.
Underpinning our focus on high-quality trial outcomes is our Patient Recruitment, Retention and Advocacy team. Our global recruitment and retention solutions provide our clients with a patient-centric, real-world approach to identifying, attracting and keeping patients involved in our trials. Ultimately, we aim to ensure that both patients and caregivers are provided with support from day one, and get access to the potentially life-saving therapeutics they need.
What you can expect
Our range of expertise, global footprint and investment in data and technology means we can provide you with –