Project Management That Keeps Your Trial On Track

From study planning to close-out, we partner with our clients as trusted advisors. Our project managers don't just coordinate the many moving parts—timelines, budgets, service providers, and submissions—they consult and support your decision-making so you can focus on strategy and science.

 
Lets plan your next study together.

Our Services

Full Study Management

  • Study design input and operational study setup 
  • Support in all stages of risk management 
  • Submission to ethics committees and regulatory authorities 
  • Continuous coordination with sites, service providers, and internal teams 
  • Sponsor consulting, communication and information 
 

Sponsor Oversight

If you need help in overseeing your internal processes and service providers, we will support your oversight activities. 

  • Identify, monitor, and mitigate risks as basis for effective oversight 
  • Set up and ensure sponsor oversight by active trial management 

Communication & Reporting

  • Build strong relationships with site teams 
  • Support the proactive identification of issues 
  • Foster open communication between sponsor, CRO, and investigators 

Full Study Management

  • Study design input and operational study setup 
  • Support in all stages of risk management 
  • Submission to ethics committees and regulatory authorities 
  • Continuous coordination with sites, service providers, and internal teams 
  • Sponsor consulting, communication and information 

Sponsor Oversight

If you need help in overseeing your internal processes and service providers, we will support your oversight activities. 

  • Identify, monitor, and mitigate risks as basis for effective oversight 
  • Set up and ensure sponsor oversight by active trial management 

Communication & Reporting

  • Build strong relationships with site teams 
  • Support the proactive identification of issues 
  • Foster open communication between sponsor, CRO, and investigators 

How We Work

  • 01Plan

    Develop timelines, budgets, and risk strategies.

  • 02Execute

    Coordinate study setup, submissions, and operations.

  • 03Monitor

    Track quality, costs, and progress with proactive reporting.

  • 04Deliver

    Ensure on-time, compliant study completion.

Why Sponsors Choose Us

Experienced Leadership

Highly skilled PMs with multi-therapy expertise. 

Pragmatic Approach

Efficient coordination without overcomplication. 

Maximum support

Partnership built on trust and transparency. 

Compliance & Training

GCP adherence
Regulatory submission expertise
Membership in national and international clinical research associations

We Assure

  • Timelines and budgets adherence
  • Constant, proactive updates—no surprises 
  • Smooth communication across the entire study team 
  • Reduced risk of deviations and delays 

How can we support you in the project management of your clinical studies?

Call Dr Doris Greiling directly right now or write us an email.

Dr Doris Greiling
+49 1520 921 96 49
info@forschungsdock.de

How can we support you in the project management of your clinical studies?

Call Dr Doris Greiling directly on +49 (0) 1520 921 96 49 or write us an email.

Contact