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, & submissions—they consult & support your decision-making so you can focus on strategy & science.

 
Lets plan your next study together.

Our Services

Full Study Management

Our team provides hands-on project management across all study stages. 

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

Sponsor Oversight

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

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

Communication & Reporting

In both scenarios, we keep you fully informed with structured updates.

  • Continuous study status reports 
  • Clear communication across stakeholders 
  • Early escalation of issues to avoid surprises 

 

Full Study Management

Our team provides hands-on project management across all study stages. 

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

Sponsor Oversight

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

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

Communication & Reporting

In both scenarios, we keep you fully informed with structured updates. 

  • Continuous study status reports 
  • Clear communication across stakeholders 
  • Early escalation of issues to avoid surprises 

How We Work

  • 01Plan

    Develop timelines, budgets, & risk strategies.

  • 02Execute

    Coordinate study setup, submissions, & operations.

  • 03Monitor

    Track quality, costs, & 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 & transparency. 

Compliance & Training

GCP adherence (ICH E6(R3), ISO 14155)
Proven track record from monosite to multinational
Membership in national & international clinical research associations

We Assure

  • Partnering & consultation early on & throughout the whole study 
  • Highly seasoned personnel with Sponsor & CRO experience 
  • Constant, proactive & transparent updates 
  • Smooth communication across the entir study team 

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