Clinical Project Management

Over 800 Assays Available

Clinical Project Management

Proven Success in Clinical Trial Project Management

QPS will meticulously manage every aspect of your late Phase II-IV clinical research, ensuring seamless coordination and oversight from initial planning through final execution. Our experienced team will handle all phases of your project, providing comprehensive management and strategic guidance to meet your study objectives efficiently and effectively.

Our project management services include:

Coordinates full range of clinical development services.
Continuous monitoring of study progress (timelines, budget, quality, organization and communication) and optimization where possible.
Development of a study protocol according to ICH GCP and local requirements/optimization of your study design.
Development of all essential study documents.
Regulatory Affairs (strategic development plan)
Timely submissions to regulatory authorities and ethics committees.
Selection, set-up and initiation of your study sites.

Organization and conduct of successful investigator meetings.
Set up and maintenance of your Trial Master File.
Closure of clinical trial.
Coordinating statistical analysis and reporting of your data.
Archiving of your study files and samples.
Individual consultancy and support in any other study related issues.

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Testimonials

We have had overall wonderful experiences with the QPS team, which is why we continue to establish new projects with you.

We are extremely grateful and pleased with all the work over the last month from Anant Pedada, Lan Li, Sarah Patterson, Dave Quirico, and all the QPS QA folks. We could not have completed any of these studies without their help and willingness to meet our tight timelines. All of our efforts right now are on our submission. If we get approved, we should have some more studies to send you.