Better Clinical Trials
Management for hire to establish and manage
- a successful CRO organization
- a successful Clinical Operation organization
Guidance on clinical development programs, strategic solutions, and
advice on how and when to facilitate CRO services.
Clinical trial applications to the Regulatory Authorities and the Ethics
Clinical Trial Management including
- feasibility studies
- building experienced well trained study teams
- rapid site selection to fit study requirements
- contracts negotiation
- efficient study start up
- facilitation of patient recruitment
- monitoring, detailed tracking and reporting of study outcome
- Seminars in drug development
- Mentorships for CRA trainees
- GCP tailor-made training courses for CRAs and Investigators
- Training for CRAs
- Training for Investigators
Arrange, prepare, and conduct investigator meetings.
Management of non-interventional studies.
Provide support for investigator driven studies e.g. protocol writing,
budgeting, submissions, contracts, and monitoring.
Helena Lomberg, PhD
Mobile: + 46(0)733319264