Why Choose TransCom for Your Clinical Trial?

Our Clinical Operations Department is composed of Project Managers, Senior CRAs, Junior CRAs, Administrative Assistants and Study-site Coordinators with extensive experience in clinical trials for pharmaceutical, medical device, biotechnology and CRO companies. All members of our Clinical Operations Department undergo intensive training and supervision by experienced clinical-trial directors during each entire study.
We define individual project-specific needs in coordination with the client, and assign precisely-tailored resources in order to meet these needs.
Throughout the study we allocate tasks according to the different specialties and level of seniority of the professionals involved. We will never allocate tasks that require a Junior CRA level staff member to high-cost Senior CRAs. If your study involves a high level of in-house administrative tasks, we will allocate a low-cost administrative assistant to ensure that the CRA does not spend time on these tasks. If your study involves sites with many patients or that may have issues with staff availability, we will allocate our own Study-site Coordinator who is committed to your study at the site.
We make proactive arrangements with the relevant medical centers to apply the same allocation and utilization models in order to maximize your “Value-for-Money”. All junior-level tasks at the medical centers are delegated to junior staff and, if necessary, we provide experienced administrative personnel to the medical centers, even at short notice, to handle a high volume of administration.
The natural outcome of our resourcing model both in-house and at the medical centers results in:

  • Maximization of CRA and Senior CRA utilization
  • Reduction of project costs

The infrastructure that we provide for every clinical study allows each staff member to focus on the specific goals. The Senior CRA supervises the study on a daily basis and assures maximum cooperation at any given point between the different staff members (both at TransCom and in the medical centers). This way, the collection and cleaning of data from the sites is faster and more efficient.
We offer flexibility in our resourcing, so we guarantee to take the best care of your business. Even if the assigned staff is replaced, or if the project requirements change during the study, we will always have the best options available for our clients.
We act as a partner to our clients, which is expressed in our:

  • High commitment to the project’s success
  • Personalized relationships based on mutual trust
  • Availability to our clients and to medical staff at investigational centers

We support our clients during each different phase of the clinical development program: starting with pivotal clinical studies, through dose-ranging studies to phase I-IV clinical studies.
Due to our unique combination of advantages, we build successful, long-term relationships with our clients.
The ingredients for this successful practice are:

  • Adaptability: As a very dynamic company, we adapt to our client’s changing needs
  • Flexibility: Every project is treated differently
  • Availability: Always available for you
  • Relationship: Personal and direct
  • Engagement: Our team “lives and breathes” the study with the client!!

 

Learn more about performing clinical trials with TransCom: