The SRC clinical operations team comprises of qualified and trained project managers, clinical team leads and monitors with extensive experience in managing phase I to IV studies for regulated markets. Our SOPs are well aligned with both regulatory norms as well as best practices of the industry. An interdisciplinary team consisting of medical, pharmaceutical and life sciences graduates under the guidance of the project manager comprises of the delivery team.
We are committed to meeting the client’s needs for quality, compliance, and agreed upon delivery times in order to achieve and, where possible, exceed the target plan with the guarantee that all work is carried out in accordance with SOPs, GCP/ICH guidelines and regulatory requirements. SRC utilizes a streamlined project management model, providing a single point of contact to oversee the people, processes and operations. For clinical studies conducted in multiple countries (SRC is conducting a number of global clinical studies with multiple centers in US, CEE and South East Asian countries), a global project manager is assigned as a single point of contact. Participating countries are managed by regional project leads/managers who communicate with the global project manager. We have also successfully completed Phase 1 clinical trials in Asian countries.
SRC offers comprehensive Phase I-IV services for drugs, devices & diagnostics. The team is well-entrenched in regulated market requirements & GCP. Our collective goal is to shrink your time-to-market through superior scientific expertise and trial management innovation.
INDIA Tel: +91 80 4262 7200
US Tel:+1 818 760 1000