Joyce Hillmer Email and Phone Number

= Provide support in planning, execution and close out of significant and non-significant risk clinical trials Assist in IRB submission, IDE and PMA  On-site monitoring including, interim monitoring and close-out visits Maintain clinical and regulatory files In-house audit and resolution of missing data/queries of informed consent forms and CRF’s for multiple sites Regular written, telephone and personal communication with study sites  Data entry and managementMy goal is to find a full time job in a small to medium medical device research company where I can use my clinical expertise and people skills