Medpace

As a global CRO with an operational footprint across 40 countries, Medpace has broad experience designing and conducting Phase I-IV clinical trials around the globe. From feasibility to patient recruitment, to study start-up, monitoring to study closure.
Medpace has local staff and management in Sweden and the surrounding Nordic countries supporting feasibility, study start-up and through the life cycle of clinical trials. In Sweden specifically, we have site relationship coordinators, contract specialists, regulatory submission specialists and our clinical research associate team.
Medpace offers thorough training for new CRAs/new employees, and at the same time offers good benefits and a great team to work with, as well as supportive management.