Enter Our Professional Way
With us hire an experienced and efficient team to assist in clinical operations support for clinical trials. Especially , Vendor Oversight, Client Team Support, Patient Recruitment, and Site Management

About us

CRDE was founded by a dedicated team of professionals with an experience in supporting pharmaceutical industry, in clinical trials related areas.

We have been supporting our clients from over 20 years. Our clients are pharmaceutical, biotech and medical devices companies as well as CROs and study sites.

We focus on delivering global training solutions, clinical operations support and staff recruitment for your clinical trials. We focus on supporting small to mid-size clients globally.

With the global experience and the expertise in wide range of clinical trials services, therapeutic areas we provide an advantage and measurable impact to our clients.

Our services, or what we do


Clinical Operations Support

Our support in Clinical Operations involves coordination between the Client and the Vendor company.

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Resourcing Solutions

We are proud to help our clients to find best talents, passionate about delivering new solutions improving patients’ health and quality of life.

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Trainings & e-Learning Solutions

We are proud to help our clients to find best talents, passionate about delivering new solutions improving patients’ health and quality of life.

Learn More >>

Clinical Operations Support

Our support in Clinical Operations involves coordination between the Client and the Vendor company. It involves establishing deliverables and timelines and CRO/Vendor Oversight Plan that includes also adopted KPIs, thresholds, KPIs monitoring, issues management and escalation.

CRO oversight include:

  • CRO identification and selection process
  • Cost proposals analysis
  • Scope of Work for clinical operations and other functions
  • Discussing the monitoring strategy and systems
  • Reviewing and approving Monitoring Plan and other plans where applicable

Reviewing on ongoing basis:

  • Monitoring visit status, issues and protocol deviations, monitoring visit report timelines and quality etc.
  • Trends based on monitoring visits report review
  • Milestone status and forecasts
  • Patient metrics
  • Site productivity
  • Enrollment metrics
  • Compliance metrics
  • Budget status
  • Performing Study Oversight Visits at the sites
  • Regular meetings with CRO functional managers
  • Issues management and escalation

Resourcing Solutions

We are proud to help our clients to find best talents, passionate about delivering new solutions improving patients’ health and quality of life. We are focused on roles involved in clinical trials: CPM, CRAs, CTAs, Data Managers etc.

Whether you need a specialist or a team, we’ll source the right person for you.

We identify experts on a global level on a permanent, freelance or multi-hire basis.
Our mission is very simple: to provide you with exceptional service as fast and successful as possible.

Trainings & e-Learning Solutions

CRDE has been providing clinical research training for over 20 years. We provide open courses as well as the ones tailored to our clients needs.

Our online trainings cover the following areas:

  • ICH GCP (E6 R2)
  • Good Documentation Practice (GDocP) and Essential Documents
  • Clinical Trial Management
  • Clinical Trial Monitoring
  • Clinical Trial Coordination and Administration
  • Regulatory

Here is the list of our currently available courses:

Here is the list of all our courses:

  • ICH GCP (E6 R2) in Ukrainian
  • ICH GCP (E6 R2) in Spanish
  • Clinical Trials Monitoring (English)
  • Good Documentation Practice and Essential Documents
  • Clinical Trial Management
  • Medical Writing
  • Drug Safety and Regulations
  • GCP refresher
  • Clinical Trial Administration

Want to know more? Just ask!

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