In acromion GmbH’s project management you will meet scientific specialists in all kind of indications and experts in clinical research. 

Serving your clinical trial, certainly our best specialist in respect of your project will continuously be the person in charge, and your personal project manager throughout the complete duration of our cooperation who will be accustomed to your individual needs and necessities.

Our project managing teams are specialists in conceptual design, organisation and coordination of all project activities. With high levels of experience, we are your adequate partner to efficiently plan and realize your clinical trial at the optimal price-performance ratio. 

Challenging projects lead us to proactive solutions, which are supervised and practically accompanied by our project management.

From project start to completion you will be cooperating with your personal project manager who is responsible for: 

Primary sponsor contact

Project planning

• preparations and start prerequisites:
• finalisation of study documents
• obtain Independent Ethics Committee/Competent Authority
• project team training
• development of study plans:
  
  • project
  • communication
  • monitoring
  • contingency
  • contract specific: safety, Clinical Data Management, Statistical Analysis Plan

Financial management

• study budget
• grant payments
• payments to third parties
• subject reimbursement

Running project to contract

• communication
• progress control
• status reporting (vs. contract, timelines, milestones)
• implementation of contingency plans and corrective measures
• quality control

Project team support

Project completion and handover of the Trial Master File