The Q Clinical Difference

​Getting a new technology to market is a complex undertaking.   But your experience working with consultants doesn't have to be.   You come to us, we discuss your needs and objectives, create a solid personalized proposal, and get to work.   It's that simple.

Not sure what you need?    Q Clinical will listen to your goals and determine how best to get there. 

our focus

Therapeutic areas

cardiology, neurology, wound care, psychiatry, endocrine, vascular, women's health, imaging, biologics, ophthalmology

Device experience

hemodialysis access, advanced wound care dressings, thermometry, peripheral vascular stents, peripheral vascular ablation devices, venous access, cardiac implant closure, cardiac laser, balloon catheters, infusion pump, robotic assist devices, imaging devices, embolic protection devices, autologous cellular therapies

our services

Clinical Strategy

It is important to have a well thought-out plan for study design for your clinical trial.  Q Clinical can liaise with the key stakeholders to develop a study design with endpoints to satisfy regulatory bodies, payors, and clinicians.  Q Clinical will provide estimates on costs and timelines of different study designs.​

Project Management

Timelines and deliverable seem to need constant managing, don't they? Let Q Clinical take the reigns. We'll work with your vendors to coordinate activities for on-time delivery of your final data set or project-specific deliverables.

Clinical Monitoring

The founding partners of Q Clinical are experienced with clinical monitoring for both drug and device trials. From a temporary study monitor to someone who can manage your contract monitors, Q Clinical is here to help with as little or as much as your project requires.

Medical Writing

Protocol writing. Regulatory reports. Scientific manuscripts. Q Clinical can provide support for all of them.  From manuscripts in journals to conference posters or presentations, we will seamlessly integrate your information and help you determine where you can get the most impact from your publication.


Let's face it: Some clinical study sites are simply better than others. Lying awake at night with concern over an FDA audit is no way to live. If this issue plagues you, send Q Clinical to the site. We'll work with the site staff and your current monitors to assess the situation and get things back on track.​ 

clinical research expertise

Study Preparation

  • Study design
  • Cost and timeline projection
  • Protocol writing
  • Clinical Advisory Boards
  • Site selection andQualification
  • Study staff training
  • Site on-boarding
  • Essential document collection
  • Budget and contracts
  • Vendor selection
  • CRF development
  • Kick-off meetings
  • Site Initiation visits

Operations/Study conduct

  • Project management
  • Site management
  • Conducting monitoring visits
  • CRA management
  • Site audit preparations
  • "Rescue" efforts
  • Vendor management
  • Medical monitoring and safety reporting
  • Refresher training
  • Interim analysis planning
  • Data management oversight
  • Data Safety Monitoring Board oversight
  • Study payments/invoicing
  • FDA annual reports
  • Data quality/site audits
  • Regulatory compliance

Study Wrap up and Completion

  • Site Close out
  • Medical and regulatory writing
  • Trial Master File maintenance and archiving
  • Publication planning and strategy