Greenline Clinical Research is a leading regional full-service contract research organization (cro) in North America providing clinical development services across all clinical trial phases and therapeutic areas and global product development and regulatory affairs consulting through our in-house team.
We provide clinical development services across all clinical trial phases and therapeutic areas including: feasibility assessments; ethics committee and regulatory submissions, data management, statistical analysis, medical monitoring, safety solutions, central lab services, report write-up to ICH requirements, project and vendor management.
Working in a fast paced and adaptable environment, we set a high benchmark for clinical trial operations by listening carefully, allocating North Region best talent, and leveraging best in class platforms, technology, systems and processes to achieve our client’s clinical program milestones and ultimately improve patient lives.
Our people are critical in meeting organisational and client’s objectives and we place a strong emphasis on creating an inclusive, collaborative, transparent and collegiate work environment where everyone is supported to learn, grow and prosper.
Our values, policies and benefits contribute to a workplace culture that reflects the supports our people to be their best in all aspects of their lives. We are committed to hiring ambitious and ethical professionals genuinely excited to be a part of the dynamic Life Sciences industry and who relish a challenge.