Performance Passion
An attitude of making it happen, drives a dedicated focus on engagement, quality, accountability and performance results
About
We've enjoyed exceptionally strong growth in recent years, expanding our footprint to provide clinical trial and drug development consulting services globally. But we remain very focused on our core mission, of being a full-service clinical development partner, specializing in biotech sector sponsors conducting trials in the North America region.
North America remains the fastest growing region in the world for clinical development but it is also a heterogenous environment with different cultures, languages, and regulatory environments. A core to our strategy is to have experienced local leadership, on-the-ground regulatory specialists, well developed KOL relationships, and monitoring presence in each of the countries in which we operate.
Our people have a deep understanding of their local environment, deep rooted relationships, and excellent English and French language capabilities.
Greenline Clinical Research is internationally recognized as the leading North America Pacific centered global biotech contract research organization (CRO).
Greenline Clinical Research has built on our deep experience and coverage across Canada with expansion into North America region and India to provide global clinical development support to our global client base.
Greenline Clinical Research has office in Canada and site partnerships with over 40 key medical institutions and experience with >1500 clinical trial sites
Greenline Clinical Research provides clinical development services across all clinical trial including regulatory and drug development consulting, protocol design and writing, feasibility assessments, local ethics committee and regulatory submissions, clinical monitoring, project and vendor management, data management, statistical analysis, data visualization and analytics, DCTs, medical advisory and medical monitoring, pharmacovigilance, central lab services and clinical study report writing. We work to the highest quality standards, in line with ICH-GCP, global regulatory agencies and underpinned by robust processes in line with our ISO 9001 accredited Quality Management system.
Greenline Clinical Research has broad therapeutic experience with a particular focus on oncology/immuno-oncology, infectious disease/vaccines, neurology, and rare diseases.
As a biotech specialist, Greenline Clinical Research has extensive medical, scientific, regulatory, and operational expertise with advanced and novel therapeutics, across all therapeutic areas, including cell & gene therapies, precision medicine, RNA based vaccines and therapeutics, ADCs, microbiome, radiopharmaceuticals and more.
Our geographic presence, our depth of expertise and services, our operational infrastructure, and investments in technological advancements, combine to provide the perfect solution to accelerate global clinical development for biotech Sponsors.
Our values and our people is what makes Greenline Clinical Research a great place to work. Our work culture is driven by our values, every day.
An attitude of making it happen, drives a dedicated focus on engagement, quality, accountability and performance results
Our style of working recognises the value of everyone involved.
We never hesitate to say or do the right thing.
We seek and nurture people with exceptional talent.
Our mission is to help bring advances in therapeutic products to market efficiently by providing high quality clinical development services to our clients. We will do this by hiring and developing highly talented people, employing the best technologies in our operations, and by fostering a culture of open communication, teamwork and sharing of knowledge, experience and resources with our internal and external partners.
A horizontal organizational structure that encourages inter-country and inter-department collaboration and knowledge-sharing is paramount. We are proud of our inclusive culture and committed to always looking for ways to improve and remain a leader in workplace flexibility and gender equality. We are continually making progress.
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