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Clinical Research Services 

The CNS provides expert consulting services to support your research at any stage.

Benefits of Working With Us

Agility

We pride ourselves in our efficiency and resourcefulness

Performance-Driven

We are meticulous and professional

Client-Centered

We want to make you a raving fan

Qualified

We are professionally certified and quality-conscious

Uncomplicated

You maintain full rights to your data and intellectual property

Our CRO Services

Study Design

From early ideation and comprehensive literature review through to outcome measure selection and statistical planning, your study will be custom-built according to your unique, long-term goals, based on ICH guidelines.

Pitch to Funders

Your study will be summarized into a brief pitch document to generate interest from potential funders and stakeholders.

Grant Writing

Find appropriate funding opportunities and let us take care of the writing and application process to help you secure the necessary resources to get your study off the ground.

REB/IRB Applications

All required documents will be prepared, including a full protocol informed consent and assent forms, and participant-facing materials (e.g. questionnaires or recruitment content), and submitted to a central or institutional ethics board for review and approval.

 Regulatory Applications

All necessary applications to Health Canada (e.g. CTA, ITA, Section 56 Exemption) and/or FDA (e.g. IND, IDE, DEA Registration) will be managed efficiently and with a high attention to detail for your Investigational Product testing needs.

Study Management

Depending on the needs of your specific protocol, we offer vendor management, international shipping coordination and support, risk management planning, participant recruitment and marketing services (e.g. graphic design, website, social media, video production, google ads), and on-site or decentralized data collection services.

 Data Management

Unique to your study needs, we will develop a custom data management plan outlining the procedures and processes for collecting, organizing, validating, analyzing, storing, and reporting data throughout the course of your study. Electronic data capture (EDC) systems and Case Report Forms (CRFs) will be designed to ensure your data is accurate, reliable, and compliant with applicable regulatory requirements.

Monitoring

Our clinical research associates offer services such as monitoring plan development, site selection and initiation, study team training, monitoring visits (remote or in-person), trial master file (TMF) development and maintenance, and study close out visits to ensure participant safety, data integrity and compliance with the protocol, applicable regulations, and good clinical practice (GCP) guidelines.

Data Analysis

From the development of an initial statistical analysis plan, through data cleaning and processing, final analysis and reporting and visualization (e.g. figures and tables), our team will provide the expertise needed to uncover the story your data is telling.

Program Evaluation

Outside the context of a clinical trial, our team can help evaluate your clinical program or intervention taking place in the real world, either prospectively or retrospectively. Let us take a deep dive into the effectiveness, efficiency, clinical relevance, and outcomes of your program, in the spirit of continuous improvement.

Medical & Scientific Writing

We are well-versed in manuscript writing and submission to medical and scientific peer reviewed journals. See our Publications for examples.

Knowledge Translation

We can turn a complex dataset into infographics, white papers, press releases, and community presentations to help share your results with the world.

Contact Us for a Quote