Coloplast - United States, Research and Development

Medical Affairs Program Manager role in Minneapolis driving clinical evidence and regulatory strategy for Coloplast. Leverage 5+ years of medical device experience to manage CERs, PMCF, and IFUs while ensuring GCP and MDR compliance. Lead cross-functional initiatives, interpret scientific data, a...

Join our Medical Affairs team in Minneapolis as a Specialist. Utilize your 5+ years of clinical research/medical affairs experience, ideally in medical devices, to drive clinical documentation and ensure regulatory compliance (ISO 14155, FDA, GCP, MDR). Serve as a clinical expert, supporting CERs...